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Mutant Prion Protein Expression Is Associated with an Alteration of the Rab GDP Dissociation Inhibitor alpha (GDI)/Rab11 Pathway
Mutations of an antibody binding energy hot spot on domain III of the dengue 2 envelope glycoprotein exploited for neutralization escape
Mutational Insights into the Roles of Amino Acid Residues in Ligand Binding for Two Closely Related Family 16 Carbohydrate Binding Modules
Mutation frequency in antibiotic-resistant and -susceptible isolates of Streptococcus pneumoniae
Mutant Huntingtin Alters Cell Fate in Response to Microtubule Depolymerization via the GEF-H1-RhoA-ERK Pathway
Mutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund-Thomson syndrome
Mutations Abrogating VP35 Interaction with Double-Stranded RNA Render Ebola Virus Avirulent in Guinea Pigs
Mutations in the Parkinson's disease genes, Leucine Rich Repeat Kinase 2 (LRRK2) and Glucocerebrosidase (GBA), are not associated with essential tremor
Mutational analyses of the BRAF, KRAS, and PIK3CA genes in oral squamous cell carcinoma
Mutation analysis of 272 Spanish families affected by autosomal recessive retinitis pigmentosa using a genotyping microarray
Mutations in the keratin 9 gene in Pakistani families with epidermolytic palmoplantar keratoderma
Mutations in Alternative Pathway Complement Proteins in American Patients with Atypical Hemolytic Uremic Syndrome
Mutational Analysis of Saccharomyces cerevisiae Erf2 Reveals a Two-step Reaction Mechanism for Protein Palmitoylation by DHHC Enzymes
Mutanobactin A from the human oral pathogen Streptococcus mutans is a cross-kingdom regulator of the yeast-mycelium transition
Mutations and Polymorphisms in the Gene Encoding Regulatory Subunit Type 1-Alpha of Protein Kinase A (PRKAR1A): An Update
Mutations in the Conserved Glycine and Serine of the MutS ABC signature motif affect Nucleotide Exchange, Kinetics of sliding clamp release of mismatch and mismatch repair
Mutant small heat shock protein B3 causes motor neuropathy Utility of a candidate gene approach
Mutations in KIT occur at low frequency in melanomas arising from anatomical sites associated with chronic and intermittent sun exposure
Mutational Analysis of Flucytosine Resistance in Candida glabrata
Mutation Discovered in a Feline Model of Human Congenital Retinal Blinding Disease
Mutations in a gene encoding a midbody protein in binucleated Reed-Sternberg cells of Hodgkin lymphoma
Mutation rates of spoligotypes and variable numbers of tandem repeat loci in Mycobacterium tuberculosis
Mutagenicity evaluation of metal oxide nanoparticles by the bacterial reverse mutation assay
Mutations in the External Loops of BK Virus VP1 and Urine Viral Load in Renal Transplant Recipients
Mutational analysis of residues important for ligand interaction with the human P2Y(12) receptor
Mutator phenotype in cancer: Origin and consequences
Mutations in Wnt2 Alter Presynaptic Motor Neuron Morphology and Presynaptic Protein Localization at the Drosophila Neuromuscular Junction
Mutations Alter the Geometry and Mechanical Properties of Alzheimer's A beta(1-40) Amyloid Fibrils
Mutation analysis (ABCC6) in a family with pseudoxanthoma elasticum: presymptomatic testing with prognostic implications
Mutations of Francisella novicida that Alter the Mechanism of Its Phagocytosis by Murine Macrophages
Mutations in MAP3K1 Cause 46,XY Disorders of Sex Development and Implicate a Common Signal Transduction Pathway in Human Testis Determination
Mutational Escape in HIV-1 CTL Epitopes Leads to Increased Binding to Inhibitory Myelomonocytic MHC Class I Receptors
Mutagenic potency of Helicobacter pylori in the gastric mucosa of mice is determined by sex and duration of infection
Mutations in Bone Marrow-Derived Stromal Stem Cells Unmask Latent Malignancy
Mutational Studies Uncover Non-Native Structure in the Dimeric Kinetic Intermediate of the H2A-H2B Heterodimer
Mutation screening of the MERIT40 gene encoding a novel BRCA1 and RAP80 interacting protein in breast cancer families
Mutagenesis of Klebsiella aerogenes UreG To Probe Nickel Binding and Interactions with Other Urease-Related Proteins
Mutations of the ER to plastid lipid transporters TGD1, 2, 3 and 4 and the ER oleate desaturase FAD2 suppress the low temperature-induced phenotype of Arabidopsis tocopherol-deficient mutant vte2
Mutation Screening Based on the Mechanical Properties of DNA Molecules Tethered to a Solid Surface
Mutagenicity of N3-methyladenine: A multi-translesion polymerase affair
Mutagenicity of a Glutathione Conjugate of Butadiene Diepoxide
Mutations in GABA(A) receptor subunits associated with genetic epilepsies
Mutational analysis of the S21 pinholin
Mutations of the Opsin Gene (Y102H and I307N) Lead to Light-induced Degeneration of Photoreceptors and Constitutive Activation of Phototransduction in Mice
Mutating the dileucine motif of the human beta(2)-adrenoceptor reduces the high initial rate of receptor phosphorylation by GRK without affecting postendocytic sorting
Mutations in the flhD gene of Escherichia coli K-12 do not cause the reported effect on cell division
Mutation analysis for RUNX1, MLL-PTD, FLT3-ITD, NPM1 and NRAS in 269 patients with MDS or secondary AML Response
Mutational analysis of Drosophila basigin function in the visual system
Mutation of the ATP Cassette Binding Transporter A1 (ABCA1) C-Terminus Disrupts HIV-1 Nef Binding but Does Not Block the Nef Enhancement of ABCA1 Protein Degradation
Mutagen sensitivity, tobacco smoking and breast cancer risk: a case-control study
Mutant INS-Gene Induced Diabetes of Youth: Proinsulin Cysteine Residues Impose Dominant-Negative Inhibition on Wild-Type Proinsulin Transport
Mutation screen of beta-crystallin genes in 274 patients with age-related macular degeneration
Mutations in the CHD7 Gene: The Experience of a Commercial Laboratory
Mutations in Lama1 Disrupt Retinal Vascular Development and Inner Limiting Membrane Formation
Mutant Prevention Concentrations of Four Carbapenems against Gram-Negative Rods
Mutations in retrotransposon AtCOPIA4 compromises resistance to Hyaloperonospora parasitica in Arabidopsis thaliana
Mutations at the same amino acid in myosin that cause either skeletal or cardiac myopathy have distinct molecular phenotypes
Mutations of DMYPT cause over constriction of contractile rings and ring canals during Drosophila germline cyst formation
Mutations in matrix and SP1 repair the packaging specificity of a Human Immunodeficiency Virus Type 1 mutant by reducing the association of Gag with spliced viral RNA
Mutagenesis Reveals the Complex Relationships between ATPase Rate and the Chaperone Activities of Escherichia coli Heat Shock Protein 70 (Hsp70/DnaK)
Mutations in the Bacillus subtilis beta Clamp That Separate Its Roles in DNA Replication from Mismatch Repair
Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules
Mutated GABA(A) receptor subunits in idiopathic generalized epilepsy
Mutations in DCC Cause Congenital Mirror Movements
Mutations in the perforin gene can be linked to macrophage activation syndrome in patients with systemic onset juvenile idiopathic arthritis
Mutations in the Gene Encoding the Ancillary Pilin Subunit of the Streptococcus suis srtF Cluster Result in Pili Formed by the Major Subunit Only
Mutation-specific hemostatic variability in mice expressing common type 2B von Willebrand disease substitutions
Mutations of the Phenylalanine Hydroxylase Gene in Iranian Azeri Turkish Patients with Phenylketonuria
Mutational Dynamics of Microsatellites
Mutated WWP1 Induces an Aberrant Expression of Myosin Heavy Chain Gene in C2C12 Skeletal Muscle Cells
Mutagenic activities of a chlorination by-product of butamifos, its structural isomer, and their related compounds
Mutation in the Q(28)SDD(31)SD site, but not in the two SQ sites of the survival of motor neuron protein, affects its foci formation
Mutations in the Cc.rmt1 gene encoding a putative protein arginine methyltransferase alter developmental programs in the basidiomycete Coprinopsis cinerea
Mutagenesis of the Rns regulator of enterotoxigenic Escherichia coli reveals roles for a linker sequence and two helix-turn-helix motifs
Mutational dynamics of murine angiogenin duplicates
Mutagenic potentials of Amberlite XAD-2-resin extracts obtained from river and drinking waters in the Northwest district of Chiba, Japan
Mutagenicity of Blue Rayon Extracts of Fish Bile as a Biomarker in a Field Study
Mutagenic activity removal of selected disperse dye by photoeletrocatalytic treatment
Mutations of Bruton's tyrosine kinase gene in Brazilian patients with X-linked agammaglobulinemia
Mutant Ferritin L-chains That Cause Neurodegeneration Act in a Dominant-negative Manner to Reduce Ferritin Iron Incorporation
Mutagenesis Studies of Human Cystathionine beta-Synthase: Residues Important for Heme Binding and Substrate Interactions
Mutational effects of different LET radiations in rpsL transgenic Arabidopsis
Mutagenicity and cytotoxicity assessment in patients undergoing orthodontic radiographs
Mutation in the xpsD gene of Xanthomonas axonopodis pv. citri affects cellulose degradation and virulence
Mutagenicity of two species of the genus Alchornea measured by Salmonella microsome assay and micronucleus test
Mutations at key pore-lining positions differentiate the water permeability of fish lens aquaporin from other vertebrates
Mutagenicity of New Lead Compounds to Treat Sickle Cell Disease Symptoms in a Salmonella/Microsome Assay
Mutations in SOX17 are Associated with Congenital Anomalies of the Kidney and the Urinary Tract
Mutational Status of Myeloproliferative Neoplasms
Mutations in Caenorhabditis elegans him-19 Show Meiotic Defects That Worsen with Age
Mutator for transforming memristor into memcapacitor
Mutant plantains (Musa spp.) with height reduction obtained by in vitro mutagenesis
Mutations and Variants in the Cohesion Factor Genes NIPBL, SMC1A, and SMC3 in a Cohort of 30 Unrelated Patients With Cornelia de Lange Syndrome
Mutations of Lysophosphatidic Acid Receptor Genes in Human Osteosarcoma Cells
Mutational Analysis of the Herpes Simplex Virus Type 1 UL25 DNA Packaging Protein Reveals Regions That Are Important after the Viral DNA Has Been Packaged
Mutation analysis of the MYO7A and CDH23 genes in Japanese patients with Usher syndrome type 1
Mutations in the Circadian Gene CLOCK in Colorectal Cancer
Mutations in the gene encoding paired box domain (PAX8) are not a frequent cause of congenital hypothyroidism (CH) in Iranian patients with thyroid dysgenesis
Mutation of the histidin residue of the DRH motif in vasopressin V2 receptor expression and function
Mutations in the rpsL Gene Are Involved in Streptomycin Resistance in Campylobacter coli
Mutation@A Glance: An Integrative Web Application for Analysing Mutations from Human Genetic Diseases
Mutated glutathione S-transferase in combination with reduced glutathione shows a synergistic effect in ameliorating oxidative stress and airway inflammation
Mutations in CHMP2B are not a cause of frontotemporal lobar degeneration in Finnish patients
Mutations in the LHX2 gene are not a frequent cause of micro/anophthalmia
Mutagenicity and genotoxicity of tannery effluents used for irrigation at Kanpur, India
Mutations in EDARADD account for a small proportion of hypohidrotic ectodermal dysplasia cases
Mutations in the Polycomb Group Gene polyhomeotic Lead to Epithelial Instability in both the Ovary and Wing Imaginal Disc in Drosophila
Mutations at the accommodation gate of the ribosome impair RF2-dependent translation termination
Mutation specific drug therapy for progressive familial or benign recurrent intrahepatic cholestasis: A new tool in a near future?
Mutations affecting the extreme C terminus of Escherichia coli haemolysin A reduce haemolytic activity by altering the folding of the toxin
Mutation and ADAMTS13-dependent modulation of disease severity in a mouse model for von Willebrand disease type 2B
Mutations of IDH1 and IDH2 genes in early and accelerated phases of myelodysplastic syndromes and MDS/myeloproliferative neoplasms
Mutations in the C-terminus of the conserved NDR kinase, Cbk1p of Saccharomyces cerevisiae, make the protein independent of upstream activators
Mutation Testing Cost Reduction Techniques: A Survey
Mutational spectrum of APC and genotype-phenotype correlations in Greek FAP patients
Mutasynthesis of Lincomycin Derivatives with Activity against Drug-Resistant Staphylococci
Mutant Mouse Models: Genotype-Phenotype Relationships to Negative Symptoms in Schizophrenia
Mutation of a Cuticle Protein Gene, BmCPG10, Is Responsible for Silkworm Non-Moulting in the 2nd Instar Mutant
Mutational analysis of 33 autosomal short tandem repeat (STR) loci in southwest Chinese Han population based on trio parentage testing
Mutational and Computational Evidence That a Nickel-Transfer Tunnel in UreD Is Used for Activation of Klebsiella aerogenes Urease
Mutation analysis of circulating plasma DNA to determine response to EGFR tyrosine kinase inhibitor therapy of lung adenocarcinoma patients
Mutational hierarchies in myelodysplastic syndromes dynamically adapt and evolve upon therapy response and failure
Mutagenesis of N-terminal residues of feline foamy virus Gag reveals entirely distinct functions during capsid formation, particle assembly, Gag processing and budding
Mutations in different pigmentation genes are associated with parallel melanism in island flycatchers
Mutations in the HECT domain of NEDD4L lead to AKT-mTOR pathway deregulation and cause periventricular nodular heterotopia
Mutations Affecting Potassium Import Restore the Viability of the Escherichia coli DNA Polymerase III holD Mutant
Mutations in actin used for structural studies partially disrupt beta-thymosin/WH2 domains interaction
Mutations Y493G and K546D in human HSP90 disrupt binding of celastrol and reduce interaction with Cdc37
Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts
Mutations in TKT Are the Cause of a Syndrome Including Short Stature, Developmental Delay, and Congenital Heart Defects
Mutation-Specific Effects on Thin Filament Length in Thin Filament Myopathy
Mutational spectrum and phenotypic variability of VCP-related neurological disease in the UK
Mutational signatures associated with tobacco smoking in human cancer
Mutations in Citron Kinase Cause Recessive Microlissencephaly with Multinucleated Neurons
Mutation Processes in 293-Based Clones Overexpressing the DNA Cytosine Deaminase APOBEC3B
Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia
Mutation in the Monocarboxylate Transporter 12 Gene Affects Guanidinoacetate Excretion but Does Not Cause Glucosuria
Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive features
Mutations in GANAB, Encoding the Glucosidase IIa Subunit, Cause Autosomal-Dominant Polycystic Kidney and Liver Disease
Mutations in genes encoding condensin complex proteins cause microcephaly through decatenation failure at mitosis
Mutations in troponin T associated with Hypertrophic Cardiomyopathy increase Ca2+-sensitivity and suppress the modulation of Ca2+-sensitivity by troponin I phosphorylation
Mutation of Fnip1 is associated with B-cell deficiency, cardiomyopathy, and elevated AMPK activity
Mutations in the Histone Modifier PRDM6 Are Associated with Isolated Nonsyndromic Patent Ductus Arteriosus
Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients
Mutational signatures of ionizing radiation in second malignancies
Mutation spectra of RAS gene family in colorectal cancer
Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis
Mutational landscape of EGFR-, MYC-, and Kras-driven genetically engineered mouse models of lung adenocarcinoma
Mutations in HECW2 are associated with intellectual disability and epilepsy
Mutation-Induced Population Shift in the MexR Conformational Ensemble Disengages DNA Binding: A Novel Mechanism for MarR Family Derepression
Mutation analysis of Swedish haemophilia B families - high frequency of unique mutations
Mutation (G275E) of the nicotinic acetylcholine receptor alpha 6 subunit is associated with high levels of resistance to spinosyns in Tuta absoluta (Meyrick) (Lepidoptera: Gelechiidae)
Mutation in the Non-coding Sequence of Badh2 Gene Reduces its Transcription and Translation in Fragrant Rice 'Nankai 138'
Mutational analysis of the Aspergillus ambient pH receptor PalH underscores its potential as a target for antifungal compounds
Mutations of KRAS/NRAS/BRAF predict cetuximab resistance in metastatic colorectal cancer patients
Mutations in MBOAT7, Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic Features
Mutations in Human Interferon alpha 2b Gene and Potential as Risk Factor Associated with Female Breast Cancer
Mutations in MSX1, PAX9 and MMP20 genes in Saudi Arabian patients with tooth agenesis
Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts
Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human Deafness
Mutational landscape of prostate tumors revealed by whole-exome sequencing
Mutations in the genes for thyroglobulin and thyroid peroxidase cause thyroid dyshormonogenesis and autosomal-recessive intellectual disability
Mutations of KRAS, NRAS, BRAF, EGFR, and PIK3CA genes in urachal carcinoma - occurence and prognostic significance
Mutation screening of the TPO gene in a cohort of 192 Chinese patients with congenital hypothyroidism
Mutations in the mevalonate pathway genes in Chinese patients with porokeratosis
Mutations of Cystic Fibrosis Transmembrane Conductance Regulator Gene Cause a Monocyte-Selective Adhesion Deficiency
Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal Dysplasia
Mutations Closer to the Active Site Improve the Promiscuous Aldolase Activity of 4-Oxalocrotonate Tautomerase More Effectively than Distant Mutations
Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis Imperfecta
Mutational analysis of anal cancers demonstrates frequent PIK3CA mutations associated with poor outcome after salvage abdominoperineal resection
Mutant swarms of a totivirus-like entities are present in the red macroalga Chondrus crispus and have been partially transferred to the nuclear genome
Mutanome and expression of immune response genes in microsatellite stable colon cancer
Mutagenic, antimutagenic, antioxidant, anti-lipoxygenase and antimicrobial activities of Scandix pecten-veneris L.
Mutations in GLDN, Encoding Gliomedin, a Critical Component of the Nodes of Ranvier, Are Responsible for Lethal Arthrogryposis
Mutational analysis of JAK2, CBL, RUNX1, and NPM1 genes in familial aggregation of hematological malignancies
Mutations in eight small DFNB genes are not a frequent cause of non-syndromic hereditary hearing loss in Czech patients
Mutation Update and Review of Severe Methylenetetrahydrofolate Reductase Deficiency
Mutations in NEBL encoding the cardiac Z-disk protein nebulette are associated with various cardiomyopathies
Mutant PI/GLO Homolog Confers the Hose-in-hose Flower Phenotype in Kurume Azaleas
Mutation in S6 domain of HCN4 channel in patient with suspected Brugada syndrome modifies channel function
Mutation analysis of EGFR and its correlation with the HPV in Indian cervical cancer patients
Mutations in the mitochondrial orf108 render Moricandia arvensis restorer ineffective in restoring male fertility to Brassica oxyrrhina-based cytoplasmic male sterile line of B. juncea
Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan Assay
Mutational prevalence of chloroquine resistance transporter gene among Plasmodium falciparum field isolates in Assam and Arunachal Pradesh, India
Mutagenicity of heteroaromatic amines: Computational study on the influence of methyl substituents
Mutations in the Schmallenberg Virus Gc Glycoprotein Facilitate Cellular Protein Synthesis Shutoff and Restore Pathogenicity of NSs Deletion Mutants in Mice
Mutagenic and genotoxic potential of direct electric current in Escherichia coli and Salmonella thyphimurium strains
Mutant IDH1 Downregulates ATM and Alters DNA Repair and Sensitivity to DNA Damage Independent of TET2
Mutagenicity of two herbicides widely used on soybean crops by the Allium cepa test
Mutations in CDC45, Encoding an Essential Component of the Pre-initiation Complex, Cause Meier-Gorlin Syndrome and Craniosynostosis
Mutation Screening of Exons 7 and 13 of the TMC1 Gene in Autosomal Recessive Non-syndromic Hearing Loss (ARNSHL) in Iran
Mutations in TSC1, TSC2, and MTOR Are Associated with Response to Rapalogs in Patients with Metastatic Renal Cell Carcinoma
Mutation in ADORA1 identified as likely cause of early-onset parkinsonism and cognitive dysfunction
Mutations in the TMCO3 Gene are Associated with Cornea Guttata and Anterior Polar Cataract
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia
Mutations reducing replication from R-loops suppress the defects of growth, chromosome segregation and DNA supercoiling in cells lacking topoisomerase I and RNase HI activity
Mutations in glucocerebrosidase are a major genetic risk factor for Parkinson's disease and increase susceptibility to dementia in a Flanders-Belgian cohort
Mutational Analysis on Membrane Associated Transporter Protein (MATP) and Their Structural Consequences in Oculocutaeous Albinism Type 4 (OCA4)A Molecular Dynamics Approach
Mutations in CEP120 cause Joubert syndrome as well as complex ciliopathy phenotypes
Mutations in exocyst complex subunit SEC6 gene impaired polar auxin transport and PIN protein recycling in Arabidopsis primary root
Mutations in two pollen self-incompatibility factors in geographically marginal populations of Solanum habrochaites impact mating system transitions and reproductive isolation
Mutations in jasmonoyl-L-isoleucine-12-hydroxylases suppress multiple JA-dependent wound responses in Arabidopsis thaliana
Mutant SOD1 protein increases Na(v)1.3 channel excitability
Mutant SOD1 protein increases Na(v)1.3 channel excitability (vol 42, pg 351, 2016)
Mutant PFN1 causes ALS phenotypes and progressive motor neuron degeneration in mice by a gain of toxicity
Mutant KRAS Conversion of Conventional T Cells into Regulatory T Cells
Mutation of the murC and murB Genes Impairs Heterocyst Differentiation in Anabaena sp Strain PCC 7120
Mutant power: using mutant allele collections for yeast functional genomics
Mutated KCNJ5 activates the acute and chronic regulatory steps in aldosterone production
Mutant DNA quantification by digital PCR can be confounded by heating during DNA fragmentation
Mutational status of IDH1 in uveal melanoma
Mutation-Driven Divergence and Convergence Indicate Adaptive Evolution of the Intracellular Human-Restricted Pathogen, Bartonella bacilliformis
Mutations to the cardiotonic steroid binding site of Na+/K+-ATPase are associated with high level of resistance to gamabufotalin in a natricine snake
Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder
Mutations in POMGNT1 cause non-syndromic retinitis pigmentosa
Mutations in pepQ Confer Low-Level Resistance to Bedaquiline and Clofazimine in Mycobacterium tuberculosis
Mutational analysis of the androgen receptor gene in two Chinese families with complete androgen insensitivity syndrome
Mutation of Growth Arrest Specific 8 Reveals a Role in Motile Cilia Function and Human Disease
Mutagenesis of S-Adenosyl-L-Methionine-Binding Residues in Coronavirus nsp14 N7-Methyltransferase Demonstrates Differing Requirements for Genome Translation and Resistance to Innate Immunity
Mutagenesis and computational docking studies support the existence of a histamine binding site at the extracellular beta 3+beta 3-interface of homooligomeric beta 3 GABA(A) receptors
Mutations Decreasing Intrinsic beta-Lactam Resistance Are Linked to Cell Division in the Nosocomial Pathogen Acinetobacter baumannii
Mutation of DNA Polymerase beta R137Q Results in Retarded Embryo Development Due to Impaired DNA Base Excision Repair in Mice
Mutational Profiles Reveal an Aberrant TGF-beta-CEA Regulated Pathway in Colon Adenomas
Mutagenicity and Pollutant Emission Factors of Solid-Fuel Cookstoves: Comparison with Other Combustion Sources
Mutations of the Sonic Hedgehog Pathway Underlie Hypothalamic Hamartoma with Gelastic Epilepsy
Mutations in HIVEP2 are associated with developmental delay, intellectual disability, and dysmorphic features
Mutational landscape of uterine and ovarian carcinosarcomas implicates histone genes in epithelial-mesenchymal transition
Mutation, Eugenics, and the Boundaries of Science
Mutant p97 exhibits species-specific changes of its ATPase activity and compromises the UBXD9-mediated monomerisation of p97 hexamers
Mutagenesis and Functional Analysis of the Bacterial Arginine Glycosyltransferase Effector NleB1 from Enteropathogenic Escherichia coli
Mutated Huntingtin Causes Testicular Pathology in Transgenic Minipig Boars
Mutations in DNMT3B Modify Epigenetic Repression of the D4Z4 Repeat and the Penetrance of Facioscapulohumeral Dystrophy
Mutation in the Hepatitis E Virus Polymerase and Outcome of Ribavirin Therapy
Mutant Tau knock-in mice display frontotemporal dementia relevant behaviour and histopathology
Mutational signatures in esophageal adenocarcinoma define etiologically distinct subgroups with therapeutic relevance
Mutagenesis testing using the LacZ reporter activity of the reparation gene mus209 in Drosophila melanogaster
Mutational and phenotypical spectrum of phenylalanine hydroxylase deficiency in Denmark
Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 function
Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects
Mutations in RIT1 cause Noonan syndrome with possible juvenile myelomonocytic leukemia but are not involved in acute lymphoblastic leukemia
Mutation screening of MIR146A/B and BRCA1/2 3 %26apos;-UTRs in the GENESIS study
Mutational Profile of 10 Afflicted Egyptian Families with 17-beta-HSD-3 Deficiency
Mutation spectrum of Egyptian children with cystic fibrosis
Mutations affecting domain V of the 23S rRNA gene in Helicobacter pylori from Cairo, Egypt
Mutational Landscape and Sensitivity to Immune Checkpoint Blockers
Mutation Update for Kabuki Syndrome Genes KMT2D and KDM6A and Further Delineation of X-Linked Kabuki Syndrome Subtype 2
Mutations in CRADD Result in Reduced Caspase-2-Mediated Neuronal Apoptosis and Cause Megalencephaly with a Rare Lissencephaly Variant
Mutational landscape, clonal evolution patterns, and role of RAS mutations in relapsed acute lymphoblastic leukemia
Mutation of the BRCA1 SQ-cluster results in aberrant mitosis, reduced homologous recombination, and a compensatory increase in non-homologous end joining (vol 6, pg 27674, 2015)
Mutations in gonadotropin-releasing hormone signaling pathway in two nIHH patients with successful pregnancy outcomes
Mutations in Dnaaf1 and Lrrc48 Cause Hydrocephalus, Laterality Defects, and Sinusitis in Mice
Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt
Mutations in the D %26apos; D3 region of VWF traditionally associated with type 1 VWD lead to quantitative and qualitative deficiencies of VWF
Mutants of Cytochrome P450 Reductase Lacking Either Gly-141 or Gly-143 Destabilize Its FMN Semiquinone
Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families
Mutation Is a Sufficient and Robust Predictor of Genetic Variation for Mitotic Spindle Traits in Caenorhabditis elegans
Mutant p53 protects ETS2 from non-canonical COP1/DET1 dependent degradation
Mutations in SLC26A1 Cause Nephrolithiasis
Mutagenic and chemical analyses provide new insight into enzyme activation and mechanism of the type 2 iron-sulfur L-serine dehydratase from Legionella pneumophila
Mutations Designed by Ensemble Defect to Misfold Conserved RNA Structures of Influenza A Segments 7 and 8 Affect Splicing and Attenuate Viral Replication in Cell Culture
Mutagenesis of Coronavirus nsp14 Reveals Its Potential Role in Modulation of the Innate Immune Response
Mutations at highly conserved residues in influenza A(H1N1)pdm09 virus affect neuraminidase activity
Mutations in a Highly Conserved Motif of nsp1 beta Protein Attenuate the Innate Immune Suppression Function of Porcine Reproductive and Respiratory Syndrome Virus
Mutation of orthologous prickle genes causes a similar epilepsy syndrome in flies and humans
Mutant Calreticulin Requires Both Its Mutant C-terminus and the Thrombopoietin Receptor for Oncogenic Transformation
Mutations in Human Accelerated Regions Disrupt Cognition and Social Behavior
Mutations in Nonessential eIF3k and eIF3l Genes Confer Lifespan Extension and Enhanced Resistance to ER Stress in Caenorhabditis elegans
Mutants at the 2-Fold Interface of Adeno-associated Virus Type 2 (AAV2) Structural Proteins Suggest a Role in Viral Transcription for AAV Capsids
Mutation Linked to Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Reduces Low-Sensitivity alpha 4 beta 2, and Increases alpha 5 alpha 4 beta 2, Nicotinic Receptor Surface Expression
Mutant Huntingtin Impairs BDNF Release from Astrocytes by Disrupting Conversion of Rab3a-GTP into Rab3a-GDP
Mutagenicity of N-acyloxy-N-alkoxyamides as an indicator of DNA intercalation part 1: evidence for naphthalene as a DNA intercalator (vol 14, pg 3699, 2016)
Mutagenicity of N-acyloxy-N-alkoxyamides as an indicator of DNA intercalation part 1: evidence for naphthalene as a DNA intercalator
Mutagenicity assessment of aerosols in emissions from domestic combustion processes
Mutation analysis of the PARKIN, PINK1, DJ1, and SNCA genes in Turkish early-onset Parkinson's patients and genotype-phenotype correlations
Mutations in the Na+/Citrate Cotransporter NaCT (SLC13A5) in Pediatric Patients with Epilepsy and Developmental Delay
Mutagenesis of Paramyxovirus Hemagglutinin-Neuraminidase Membrane-Proximal Stalk Region Influences Stability, Receptor Binding, and Neuraminidase Activity
Mutant cycle analysis with modified saxitoxins reveals specific interactions critical to attaining high-affinity inhibition of hNa(V)1.7
Mutations in Cockayne Syndrome-Associated Genes (Csa and Csb) Predispose to Cisplatin-Induced Hearing Loss in Mice
Mutation of the Dyslexia-Associated Gene Dcdc2 Enhances Glutamatergic Synaptic Transmission Between Layer 4 Neurons in Mouse Neocortex
Mutations at the Subunit Interface of Yeast Proliferating Cell Nuclear Antigen Reveal a Versatile Regulatory Domain
Mutational Biases Drive Elevated Rates of Substitution at Regulatory Sites across Cancer Types
Mutations in succinate dehydrogenase B (SDHB) enhance neutrophil survival independent of HIF-1 alpha expression
mutation3D: Cancer Gene Prediction Through Atomic Clustering of Coding Variants in the Structural Proteome
Mutations in LTBP3 cause acromicric dysplasia and geleophysic dysplasia
Mutations in TrkA Causing Congenital Insensitivity to Pain with Anhidrosis (CIPA) Induce Misfolding, Aggregation, and Mutation-dependent Neurodegeneration by Dysfunction of the Autophagic Flux
Mutations and deletions of PRC2 in prostate cancer
Mutation of the Enterohemorrhagic Escherichia coli Core LPS Biosynthesis Enzyme RfaD Confers Hypersusceptibility to Host Intestinal Innate Immunity In vivo
Mutation distributions and clinical correlations of PIK3CA gene mutations in breast cancer
Mutation status of essential thrombocythemia and primary myelofibrosis defines clinical outcome
Mutant prevention concentration of colistin alone and in combination with rifampicin for multidrug-resistant Acinetobacter baumannii
Mutational analysis of the Potyviridae transcriptional slippage site utilized for expression of the P3N-PIPO and P1N-PISPO proteins
Mutations associated with familial Parkinson's disease alter the initiation and amplification steps of alpha-synuclein aggregation
Mutation of the key residue for extraribosomal function of ribosomal protein S19 cause increased grooming behaviors in mice
Mutations in epigenetic modifiers in acute myeloid leukemia and their clinical utility
Mutations in gyrA and gyrB among Fluoroquinolone- and Multidrug-Resistant Mycobacterium tuberculosis Isolates
Mutational Analysis of the Binding-Induced Folding Reaction of the Mixed-Lineage Leukemia Protein to the KIX Domain
Mutation rates and the evolution of germline structure
Mutation Rates and Discriminating Power for 13 Rapidly-Mutating Y-STRs between Related and Unrelated Individuals
Mutation analysis of the MS4A and TREM gene clusters in a case-control Alzheimer%26apos;s disease data set
Mutational History of a Human Cell Lineage from Somatic to Induced Pluripotent Stem Cells
Mutational patterns in oncogenes and tumour suppressors
Mutagenesis for improvement of activity and thermostability of amylomaltase from Corynebacterium glutamicum
Mutational Studies of Putative Biosynthetic Genes for the Cyanobacterial Sunscreen Scytonemin in Nostoc punctiforme ATCC 29133
Mutations analysis of RAB39B gene in Chinese early-onset Parkinson's disease
Mutant neurogenin-3 in a Turkish boy with congenital malabsorptive diarrhea
Mutation of the Traj18 gene segment using TALENs to generate Natural Killer T cell deficient mice
Mutational Spectrum of CYP24A1 Gene in a Cohort of Italian Patients with Idiopathic Infantile Hypercalcemia
Mutations of TP53 gene in adult acute lymphoblastic leukemia at diagnosis do not affect the achievement of hematologic response but correlate with early relapse and very poor survival
Mutation analysis of the phospholamban gene in 315 South Africans with dilated, hypertrophic, peripartum and arrhythmogenic right ventricular cardiomyopathies (vol 6, 22235, 2016)
Mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia: a report from the Italian AIEOP study group
Mutagenesis and Biotechnology Techniques as Tools for Selecting New Stable Diploid and Tetraploid Olive Genotypes and Their Dwarfing Agronomical Characterization
Mutational spectrum and risk stratification of intermediate-risk acute myeloid leukemia patients based on next-generation sequencing
Mutagenicity and preclinical safety assessment of the aqueous extract of Clinacanthus nutans leaves
Mutagenic induction of an ultra-fast water-chain proton wire
Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects
Mutation in West Nile Virus Structural Protein prM during Human Infection
Mutational analysis of PI3K/AKT and RAS/RAF pathway activation in malignant salivary gland tumours with a new mutation of PIK3CA
Mutational scanning reveals the determinants of protein insertion and association energetics in the plasma membrane
Mutations in the Plasmodium falciparum Cyclic Amine Resistance Locus (PfCARL) Confer Multidrug Resistance
Mutation analysis of GLDC, AMT and GCSH in cataract captive-bred vervet monkeys (Chlorocebus aethiops)
Mutations in BRAT1 cause autosomal recessive progressive encephalopathy: Report of a Spanish patient
Mutagenic properties of linuron and chlorbromuron evaluated by means of cytogenetic biomarkers in mammalian cell lines
Mutations affecting the internal equilibrium of the reaction catalyzed by 6-aminohexanoate-dimer hydrolase
Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese population
Mutations of the EGFR, K-ras, EML4-ALK, and BRAF genes in resected pathological stage I lung adenocarcinoma
Mutation tendency of mutator Plasmodium berghei with proofreading-deficient DNA polymerase delta
Mutation design of a thermophilic Rubisco based on three-dimensional structure enhances its activity at ambient temperature
Mutations in the G-domain of Ski7 cause specific dysfunction in non-stop decay
Mutant allele of rna14 in fission yeast affects pre-mRNA splicing
Mutation of heme c axial ligands in D-fructose dehydrogenase for investigation of electron transfer pathways and reduction of overpotential in direct electron transfer-type bioelectrocatalysis
Mutational analysis of hepatitis B virus pre-S1 (9-24) fusogenic peptide
Mutation analysis of MUTYH in Japanese colorectal adenomatous polyposis patients
Mutant p53 inhibits miRNA biogenesis by interfering with the microprocessor complex
Mutant p53 proteins alter cancer cell secretome and tumour microenvironment: Involvement in cancer invasion and metastasis
Mutational analysis of structural elements in a class-I cyclic di-GMP riboswitch to elucidate its regulatory mechanism
Mutant p53 proteins counteract autophagic mechanism sensitizing cancer cells to mTOR inhibition
Mutations of the cluster algebra of type A(1)((1)) and the periodic discrete Toda lattice
Mutant p53 and mTOR/PKM2 regulation in cancer cells
Mutational characteristics of ANK1 and SPTB genes in hereditary spherocytosis
Mutational spectrum of Korean patients with corneal dystrophy
Mutation of a conserved tryptophan residue in the CBM3c of a GH9 endoglucanase inhibits activity
Mutations in XRCC4 cause primordial dwarfism without causing immunodeficiency
Mutations in ash1 and trx enhance P-element-dependent silencing in Drosophila melanogaster
Mutation in the gene encoding 1-aminocyclopropane-1-carboxylate synthase 4 (CitACS4) led to andromonoecy in watermelon
Mutation Scanning of D1705 and D1709 in the RNAse IIIb Domain of MicroRNA Processing Enzyme Dicer in Cutaneous Melanoma
Mutant desmin substantially perturbs mitochondrial morphology, function and maintenance in skeletal muscle tissue
Mutational analysis of primary and metastatic colorectal cancer samples underlying the resistance to cetuximab-based therapy
Mutations causative of familial hypercholesterolaemia: screening of 98 098 individuals from the Copenhagen General Population Study estimated a prevalence of 1 in 217
Mutations in the Motile Cilia Gene DNAAF1 Are Associated with Neural Tube Defects in Humans
Mutational screening of the INSL3 gene in azoospermic males with a history of cryptorchidism
Mutation in lamin A/C sensitizes the myocardium to exercise-induced mechanical stress but has no effect on skeletal muscles in mouse
Mutations in the glucocerebrosidase gene are common in patients with Parkinson's disease from Eastern Canada
Mutational analysis of FANCJ helicase
Mutation of Aryl Binding Pocket Residues Results in an Unexpected Activity Switch in an Oryza sativa Tyrosine Aminomutase
Mutation of Serine 32 to Threonine in Peroxiredoxin 6 Preserves Its Structure and Enzymatic Function but Abolishes Its Trafficking to Lamellar Bodies
Mutation/SNP analysis in EF-hand calcium binding domain of mitochondrial Ca2+ uptake 1 gene in bipolar disorder patients
Mutational Spectrum of the MEFV Gene in AA Amyloidosis Associated With Familial Mediterranean Fever
Mutation profiling of 19 candidate genes in acute myeloid leukemia suggests significance of DNMT3A mutations
Mutation specific immunohistochemistry is highly specific for the presence of calreticulin mutations in myeloproliferative neoplasms
Mutations of Vasopressin Receptor 2 Including Novel L312S Have Differential Effects on Trafficking
Mutation of wrb, a Component of the Guided Entry of Tail-Anchored Protein Pathway, Disrupts Photoreceptor Synapse Structure and Function
Mutant bacterial sodium channels as models for local anesthetic block of eukaryotic proteins
Mutation analysis of the CHCHD2 gene in Chinese Han patients with Parkinson's disease
Mutation Analysis of Gap Junction Protein Beta 1 and Genotype-Phenotype Correlation in X-linked Charcot-Marie-Tooth Disease in Chinese Patients
Mutation of rnf213a by TALEN causes abnormal angiogenesis and circulation defects in zebrafish
Mutations and expression of the NFE2L2/KEAP1/CUL3 pathway in Chinese patients with lung squamous cell carcinoma
Mutational Analysis of TCOF1, GSC, and HOXA2 in Patients With Treacher Collins Syndrome
Mutation analysis of 19 autosomal short tandem repeats in Chinese Han population from Shanghai
Mutation Analysis of MR-1, SLC2A1, and CLCN1 in 28 PRRT2-negative Paroxysmal Kinesigenic Dyskinesia Patients
Mutagenic effects of carbon ion beam irradiations on dry Lotus japonicus seeds
Mutations of charged amino acids at the cytoplasmic end of transmembrane helix 2 affect transport activity of the budding yeast multidrug resistance protein Pdr5p
Mutation Spectrum of the Survival of Motor Neuron 1 and Functional Analysis of Variants in Chinese Spinal Muscular Atrophy
Mutational profiling of non-small-cell lung cancer patients resistant to first-generation EGFR tyrosine kinase inhibitors using next generation sequencing
Mutational analysis of CHCHD2 in Chinese patients with multiple system atrophy and amyotrophic lateral sclerosis
Mutation analysis and prenatal diagnosis in a Chinese family with succinic semialdehyde dehydrogenase and a systematic review of the literature of reported ALDH5A1 mutations
Mutation spectrum of TP53 gene predicts clinicopathological features and survival of gastric cancer
Mutations Causing Slow-Channel Myasthenia Reveal That a Valine Ring in the Channel Pore of Muscle AChR is Optimized for Stabilizing Channel Gating
Mutational burdens and evolutionary ages of thyroid follicular adenoma are comparable to those of follicular carcinoma
Mutation of Rice Early Flowering3.1 (OsELF3.1) delays leaf senescence in rice
Mutagenicity and Immune Toxicity of Emulsion-type Sausage Cured with Plasma-treated Water
Mutations in SLC12A3 and CLCNKB and Their Correlation with Clinical Phenotype in Patients with Gitelman and Gitelman-like Syndrome (vol 31, pg 47, 2016)
Mutated form (G52E) of inactive diphtheria toxin CRM197: molecular simulations clearly display effect of the mutation to NAD binding
Mutation Spectrum and Phenotypic Features in Noonan Syndrome with PTPN11 Mutations: Definition of Two Novel Mutations
Mutation of AN39-1 for production and characterization of constitutive, thermostable and pH-resistant dextransucrase
Mutations in DNAJB13, Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility
Mutational and clinical analysis of the ENG gene in patients with pulmonary arterial hypertension
母胎医学研究进展
木炭对垃圾渗沥液中COD的吸附性能研究
木炭填料生物反应器对微囊藻毒素的去除
木糖醇对发酵香肠水分及微生物的影响
木炭研究方法
木炭高温水蒸气气化的模拟分析
木糖氧化无色杆菌P1对芘降解的研究及其在两相分配生物反应系统中的应用
木糖醇部分替代蔗糖对蜜汁叉烧肉品质的影响
木糖醇发酵的随机延迟微分方程模型分析
钼钛锆高温合金的电火花加工工艺研究
木糖醇对大豆分离蛋白结构和起泡特性的影响
Mutator转座子介导的玉米甜质突变体侧翼序列克隆
木糖醇酸奶的发酵工艺研究
木糖对产油假丝酵母油脂积累的影响
Mutations remote from the human gonadotropin-releasing hormone (GnRH) receptor-binding sites specifically increase binding affinity for GnRH II but not GnRH I - Evidence for ligand-selective, receptor-active conformations
木炭催化甘油重整制氢研究
Mutagenic and Estrogenic Effects of Organic Compounds in Water Treated by Different Processes: A Pilot Study
Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice
Mutant connexin 50 (S276F) inhibits channel and hemichannel functions inducing cataract
Mutational analysis of hepatitis E virus ORF1 "Y-domain": Effects on RNA replication and virion infectivity
Mutations affecting beta-tubulin folding and degradation
Mutations at leucine 215 of beta-tubulin affect paclitaxel sensitivity by two distinct mechanisms
Mutations in alpha- and beta-tubulin that stabilize microtubules and confer resistance to Colcemid and vinblastine
Mutations in GJA1(connexin 43) are associated with non-syndromic autosomal recessive deafness
Mutational analysis to identify the residues essential for the inhibition of N-acetyl glutamate kinase of Corynebacterium glutamicum
Mutation and prognostic analyses of PIK3CA in patients with completely resected lung adenocarcinoma
Mutation detection in Chinese patients with familial hypercholesterolemia
Mutagenicity of polluted reservoir water and its reduction by a pilot-scale integrated biological treatment process
Mutant Allele-Specific Uncoupling of PENETRATION3 Functions Reveals Engagement of the ATP-Binding Cassette Transporter in Distinct Tryptophan Metabolic Pathways
Mutation induced enhancement of Al tolerance in barley cell lines
Mutational analyses of human eIF5A-1-identification of amino acid residues critical for eIF5A activity and hypusine modification
Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation
木糖还原酶定点突变设计的生物信息学分析
Mutational analyses of the p35-caspase interaction - A bowstring kinetic model of caspase inhibition by p35
木糖醇对糖尿病大鼠骨生物力学的影响
木糖醇对糖尿病模型大鼠骨形态计量学的影响
穆涛:风韵疏淡,乘物以游心
木炭蚊香可减少有毒物质的释放(详细摘要)
木糖氧化无色杆菌及混合菌群对多环芳烃的降解特性
木糖醇对唾液和菌斑中变形链球菌的影响
木炭还原氧化铜实验成功的关键再探
Mutations in dynein genes in patients affected by isolated non-syndromic asthenozoospermia
Mutations in H5N1 Influenza Virus Hemagglutinin that Confer Binding to Human Tracheal Airway Epithelium
Mutant Presenilin 2 Increases beta-Secretase Activity Through Reactive Oxygen Species-Dependent Activation of Extracellular Signal-Regulated Kinase
Mutations That Alter Use of Hepatitis C Virus Cell Entry Factors Mediate Escape From Neutralizing Antibodies
Mutant Alleles of Photoperiod-1 in Wheat (Triticum aestivum L.) That Confer a Late Flowering Phenotype in Long Days
Mutations of Mitochondrial DNA in Atherosclerosis and Atherosclerosis-Related Diseases
Mutational analysis of telomere genes in BRCA1/2-negative breast cancer families with very short telomeres
Mutation of SH2B3 (LNK), a Genome-Wide Association Study Candidate for Hypertension, Attenuates Dahl Salt-Sensitive Hypertension via Inflammatory Modulation
Mutations in inhibin and activin genes associated with human disease
Mutation in the Flavin Mononucleotide Domain Modulates Magnetic Circular Dichroism Spectra of the iNOS Ferric Cyano Complex in a Substrate-Specific Manner
Mutational complex genotype of the hepatitis B virus X/precore regions as a novel predictive marker for hepatocellular carcinoma
Mutations in the Arabidopsis Peroxisomal ABC Transporter COMATOSE Allow Differentiation between Multiple Functions In Planta: Insights from an Allelic Series
Mutations in ABCD4 cause a new inborn error of vitamin B-12 metabolism
Mutagenicity of smoke condensates from Canadian cigarettes with different design features
Mutation of Cys242 of Human Monoacylglycerol Lipase Disrupts Balanced Hydrolysis of 1-and 2-Monoacylglycerols and Selectively Impairs Inhibitor Potency
Mutant TDP-43 in motor neurons promotes the onset and progression of ALS in rats
Mutation Rates and Intrinsic Fidelity of Retroviral Reverse Transcriptases
Mutations that reduce its specific DNA binding inhibit high NaCl-induced nuclear localization of the osmoprotective transcription factor NFAT5
Mutations in DNA-Binding Loop of NFAT5 Transcription Factor Produce Unique Outcomes on Protein-DNA Binding and Dynamics
Mutation in dystrophin-encoding gene affects energy metabolism in mouse myoblasts
Mutator phenotypes due to DNA replication infidelity
Mutant LRRK2 Toxicity in Neurons Depends on LRRK2 Levels and Synuclein But Not Kinase Activity or Inclusion Bodies
Mutation C677 T research in gene coding for methylene tetrahydrofolate reductase (MTHFR) in neural tube defects (NTDs) in Constantine
Mutations in epigenetic modifiers in the pathogenesis and therapy of acute myeloid leukemia
Mutations in epigenetic regulators in myelodysplastic syndromes
Mutational Determinants of Epigenetic Instablity in Myeloid Malignancies
Mutational analysis of residues involved in nucleotide and divalent cation stabilization in the rotavirus RNA-dependent RNA polymerase catalytic pocket
Mutated Ptpn11 alters leukemic stem cell frequency and reduces the sensitivity of acute myeloid leukemia cells to Mcl1 inhibition
Mutation in PIGA Results in a CD52-Negative Escape Variant in a Sezary Syndrome Patient during Alemtuzumab Treatment
Mutations in Prickle Orthologs Cause Seizures in Flies, Mice, and Humans
Mutations in two genes on chromosome 13 resulting in a complex hair and skin phenotype due to two rare genodermatoses: KLICK and autosomal recessive woolly hair/hypotrichosis simplex
Mutation in OsLMS, a gene encoding a protein with two double-stranded RNA binding motifs, causes lesion mimic phenotype and early senescence in rice (Oryza sativa L.)
Mutation Spectrum in the Large GTPase Dynamin 2, and Genotype-Phenotype Correlation in Autosomal Dominant Centronuclear Myopathy
Mutations in TDP-43 link glycine-rich domain functions to amyotrophic lateral sclerosis
Mutant induced pluripotent stem cell lines recapitulate aspects of TDP-43 proteinopathies and reveal cell-specific vulnerability
Mutations Within Enhancer II and BCP Regions of Hepatitis B Virus in Relation to Advanced Liver Diseases in Patients Infected With Subgenotype B3 in Indonesia
Mutation analysis of mitochondrial DNA 12SrRNA and tRNASer(UCN) genes in non-syndromic hearing loss patients
Mutation Detection and Accurate Diagnosis of Extensively Drug-Resistant Tuberculosis: Report from a Tertiary Care Center in India
Mutagenic Repair of DNA Interstrand Crosslinks
Mutations in CIZ1 cause adult onset primary cervical dystonia
Mutations and Deletions of the TP53 Gene Predict Nonresponse to Treatment and Poor Outcome in First Relapse of Childhood Acute Lymphoblastic Leukemia
Mutant PRPS1: a new therapeutic target in relapsed acute lymphoblastic leukemia
Mutational analysis of HOXA2 and SIX2 in a Bronx population with isolated microtia
Mutator effects and mutation signatures of editing deaminases produced in bacteria and yeast
Mutations in HFE Causing Hemochromatosis Are Associated with Primary Hypertriglyceridemia
Mutations in TRPM1 Are a Common Cause of Complete Congenital Stationary Night Blindness
Mutation of the Protein Kinase C Site in Borna Disease Virus Phosphoprotein Abrogates Viral Interference with Neuronal Signaling and Restores Normal Synaptic Activity
Mutagenesis by imprecise excision of the piggyBac transposon in Drosophila melanogaster
Mutation Analysis of SLC26A4 for Pendred Syndrome and Nonsyndromic Hearing Loss by High-Resolution Melting
Mutant p53 Protein Is Targeted by Arsenic for Degradation and Plays a Role in Arsenic-mediated Growth Suppression
Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from Pakistan
Mutations in lipase H cause autosomal recessive hypotrichosis simplex with woolly hair
Mutational analysis of JAG1 gene in non-syndromic Tetralogy of Fallot children
Mutant superoxide dismutase-1 indistinguishable from wild-type causes ALS
Mutagenesis of Varicella-Zoster Virus Glycoprotein I (gI) Identifies a Cysteine Residue Critical for gE/gI Heterodimer Formation, gI Structure, and Virulence in Skin Cells
Mutations in VP2 and VP1 capsid proteins increase infectivity and mouse lethality of enterovirus 71 by virus binding and RNA accumulation enhancement
Mutations in genes encoding complement inhibitors CD46 and CFH affect the age at nephritis onset in patients with systemic lupus erythematosus
Mutation in TACO1, encoding a translational activator of COX I, results in cytochrome c oxidase deficiency and late-onset Leigh syndrome
Mutations in Rice (Oryza sativa) Heavy Metal ATPase 2 (OsHMA2) Restrict the Translocation of Zinc and Cadmium
Mutation Hot Spots in Yeast Caused by Long-Range Clustering of Homopolymeric Sequences
Mutations in BMP4 Are Associated with Subepithelial, Microform, and Overt Cleft Lip
Mutations in the Amino Terminus of Herpes Simplex Virus Type 1 gL Can Reduce Cell-Cell Fusion without Affecting gH/gL Trafficking
Mutagenic Analysis of the Clostridium difficile Flagellar Proteins, FliC and FliD, and Their Contribution to Virulence in Hamsters
Mutational Effects on Transglycosylating Activity of Family 18 Chitinases and Construction of a Hypertransglycosylating Mutant
Mutation of Herpesvirus Saimiri ORF51 Glycoprotein Specifically Targets Infectivity to Hepatocellular Carcinoma Cell Lines
Mutations in MAPT Gene Cause Chromosome Instability and Introduce Copy Number Variations Widely in the Genome
Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome
Mutational properties of amino acid residues: implications for evolvability of phosphorylatable residues
Mutation scanning-based analysis of anisakid larvae from Sillago flindersi from Bass Strait, Australia
Mutator Mutations Enhance Tumorigenic Efficiency across Fitness Landscapes
Mutational analysis of quinolone resistance in the plasmid-encoded pentapeptide repeat proteins QnrA, QnrB and QnrS
Mutation in the TCR alpha subunit constant gene (TRAC) leads to a human immunodeficiency disorder characterized by a lack of TCR alpha beta(+) T cells
Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy
Mutations in Exon 3 of the CTNNB1 Gene (beta-Catenin Gene) in Cutaneous Adnexal Tumors
Mutation in Pyrroline-5-Carboxylate Reductase 1 Gene in Families with Cutis Laxa Type 2
Mutation in the mitochondrial tRNA(va1) causes mitochondrial encephalopathy, lactic acidosis and stroke-like episodes
Mutant Plant Viruses with Cell Binding Motifs Provide Differential Adhesion Strengths and Morphologies
Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation
Mutant DISC1 affects methamphetamine-induced sensitization and conditioned place preference: a comorbidity model
Mutational landscape of gingivo-buccal oral squamous cell carcinoma reveals new recurrently-mutated genes and molecular subgroups
Mutation discovery for crop improvement
Mutations in the Gene PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions
Mutation screening of IRF6 among families with non-syndromic oral clefts and identification of two novel variants: Review of the literature
Mutation D816V Alters the Internal Structure and Dynamics of c-KIT Receptor Cytoplasmic Region: Implications for Dimerization and Activation Mechanisms
Mutagenesis and phenotypic selection as a strategy toward domestication of Chlamydomonas reinhardtii strains for improved performance in photobioreactors
Mutations in the GATA4 gen in patients with non-syndromic congenital heart disease
Mutations in the B30.2 domain of pyrin and the risk of ankylosing spondylitis in the Chinese Han population: A case-control study
Mutagenic Primer Design for Mismatch PCR-RFLP SNP Genotyping Using a Genetic Algorithm
Mutations in CBL occur frequently in juvenile myelomonocytic leukemia
Mutational analysis of conserved outer sphere arginine residues of chalcone synthase
Mutational analysis of the HIV-1 auxiliary protein Vif identifies independent domains important for the physical and functional interaction with HIV-1 reverse transcriptase
Mutation analysis of the SLC26A4, FOXI1 and KCNJ10 genes in individuals with congenital hearing loss
Mutational analysis of human heat-shock transcription factor 1 reveals a regulatory role for oligomerization in DNA-binding specificity
Mutation-selection dynamics and error threshold in an evolutionary model for Turing machines
Mutation Rates and Intraspecific Divergence of the Mitochondrial Genome of Pristionchus pacificus
Mutation Rate Inferred From Synonymous Substitutions in a Long-Term Evolution Experiment With Escherichia coli
Mutational bias is the driving force for shaping the synonymous codon usage pattern of alternatively spliced genes in rice (Oryza sativa L.)
Mutational analysis of white spruce (Picea glauca) ent-kaurene synthase (PgKS) reveals common and distinct mechanisms of conifer diterpene synthases of general and specialized metabolism
Mutational frequencies in usherin (USH2A gene) in 26 Colombian individuals with Usher syndrome type II
Mutations in the Myostatin gene leading to hypermuscularity in mammals: indications for a similar mechanism in fish?
Mutation in the type IB bone morphogenetic protein receptor alk6b impairs germ-cell differentiation and causes germ-cell tumors in zebrafish
Mutational Hotspots in the Mitochondrial D-Loop Region of Cancerous and Precancerous Colorectal Lesions in Egyptian Patients
Mutations of the thyroglobulin gene and its relevance to thyroid disorders
Mutation spectrum of hepatocellular carcinoma from eastern-European patients betrays the impact of a complex exposome
Mutations in TP53, CTNNB1 and PIK3CA genes in hepatocellular carcinoma associated with hepatitis B and hepatitis C virus infections
Mutations in human monoamine-related neurotransmitter pathway genes
Mutant-prevention concentration and mechanism of resistance in clinical isolates and enrofloxacin/marbofloxacin-selected mutants of Escherichia coli of canine origin
Mutational screening of SF1 and WNT4 in Tunisian women with premature ovarian failure
Mutations in the highly conserved SLQYLA motif of Vif in a simian-human immunodeficiency virus result in a less pathogenic virus and are associated with G-to-A mutations in the viral genome
Mutation and Clinical Characteristics of Autosomal-Dominant Hereditary Spastic Paraplegias in China
Mutant GlialCAM Causes Megalencephalic Leukoencephalopathy with Subcortical Cysts, Benign Familial Macrocephaly, and Macrocephaly with Retardation and Autism
Mutations in the spike gene of porcine epidemic diarrhea virus associated with growth adaptation in vitro and attenuation of virulence in vivo
Mutations in the Predicted Active Site of Xanthomonas oryzae pv. oryzae XopQ Differentially Affect Virulence, Suppression of Host Innate Immunity, and Induction of the HR in a Nonhost Plant
Mutations in sodium-channel gene SCN9A cause a spectrum of human genetic pain disorders
Mutational survey of recessive dystrophic epidermolysis bullosa in Tunisian families unveils a spectrum of private, ethnic specific and world wide recurrent mutations
Mutation Mechanisms
Mutator System Derivatives Isolated from Sugarcane Genome Sequence
Mutational Analysis of the PHEX Gene: Novel Point Mutations and Detection of Large Deletions by MLPA in Patients with X-Linked Hypophosphatemic Rickets
Mutant human APP exacerbates pathology in a mouse model of NPC and its reversal by a beta-cyclodextrin
Mutant Protein A30P alpha-Synuclein Adopts Wild-type Fibril Structure, Despite Slower Fibrillation Kinetics
Mutation-dependent Polymorphism of Cu,Zn-Superoxide Dismutase Aggregates in the Familial Form of Amyotrophic Lateral Sclerosis
Mutations in the Human Homeobox MSX1 Gene in the Congenital Lack of Permanent Teeth
Mutations in BMP4 cause eye, brain, and digit developmental anomalies: Overlap between the BMP4 and hedgehog signaling pathways
Mutations in Multiple XXT Genes of Arabidopsis Reveal the Complexity of Xyloglucan Biosynthesis
Mutations that affect mitochondrial functions and their association with neurodegenerative diseases
Mutation breeding of sweet potato by gamma-ray radiation
Mutant Native Outer Membrane Vesicles Combined with a Serogroup A Polysaccharide Conjugate Vaccine for Prevention of Meningococcal Epidemics in Africa
Mutation-associated fusion cancer genes in solid tumors
Mutational analysis reveals a dual role of Mdm2 acidic domain in the regulation of p53 stability
Mutation of the His ligand in mitoNEET stabilizes the 2Fe-2S cluster despite conformational heterogeneity in the ligand environment
Mutational analysis of conserved aspartic acid residues in the Methanothermobacter thermautotrophicus MCM helicase
Mutations in Niemann Pick type C gene are risk factor for Alzheimer's disease
Mutational analysis of GIGYF2, ATP13A2 and GBA genes in Brazilian patients with early-onset Parkinson's disease
Mutations in the glucocerebrosidase gene confer a risk for Parkinson disease in North Africa
Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosis
Mutation Spectrum in FE1-Muta (TM) Mouse Lung Epithelial Cells Exposed to Nanoparticulate Carbon Black
Mutation Screening of the gamma-Aminobutyric Acid Type-A Receptor Subunit gamma 2 Gene in Korean Patients with Childhood Absence Epilepsy
Mutagenesis and biochemical studies on AuaA confirmed the importance of the two conserved aspartate-rich motifs and suggested difference in the amino acids for substrate binding in membrane-bound prenyltransferases
Mutations in familial nocturnal frontal lobe epilepsy might be associated with distinct neurological phenotypes
Mutation-based growth charts for SEDC and other COL2A1 related dysplasias
Mutational Bias Plays an Important Role in Shaping Longevity-Related Amino Acid Content in Mammalian mtDNA-Encoded Proteins
Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome
Mutation Screening of Mitochondrial DNA as Well as OPA1 and OPA3 in a Chinese Cohort With Suspected Hereditary Optic Atrophy
Mutations in Multiple PKD Genes May Explain Early and Severe Polycystic Kidney Disease
Mutagenicity, Genotoxicity, and Estrogenic Activity of River Porewaters
Mutation in gap and tight junctions in patients with non-syndromic hearing loss
Mutation Analysis of Familial GJB2-Related Deafness in Iranian Azeri Turkish Patients
Mutation of the NADH Oxidase Gene (nox) Reveals an Overlap of the Oxygen- and Acid-Mediated Stress Responses in Streptococcus mutans
Mutation of a degS Homologue in Enterobacter cloacae Decreases Colonization and Biological Control of Damping-Off on Cucumber
Mutations in Genes patA and patL of Anabaena sp Strain PCC 7120 Result in Similar Phenotypes, and the Proteins Encoded by Those Genes May Interact
Mutagenic effect of Bisphenol A on adult rat male germ cells and their fertility
Mutations of the ALS gene endowing resistance to ALS-inhibiting herbicides in Lolium rigidum populations
Mutational Analysis Reveals a Single Binding Interface between RhoA and Its Effector, PRK1
Mutations and epimutations in the origin of cancer
Mutations in proteins of the Conserved Oligomeric Golgi Complex affect polarity, cell wall structure, and glycosylation in the filamentous fungus Aspergillus nidulans
Mutations in microRNA Binding Sites of CEP Genes Involved in Cancer
Mutations in HISTONE ACETYLTRANSFERASE1 affect sugar response and gene expression in Arabidopsis
Mutations in the SPARC-Related Modular Calcium-Binding Protein 1 Gene, SMOC1, Cause Waardenburg Anophthalmia Syndrome
Mutational Screening of the SOCS3 Gene Promoter in Metastatic Colorectal Cancer Patients
Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy
Mutations of small heat shock proteins and human congenital diseases
Mutant Huntingtin induces activation of the Bcl-2/adenovirus E1B 19-kDa interacting protein (BNip3)
Mutation spectrum of CYP1B1 and MYOC genes in Korean patients with primary congenital glaucoma
Mutagenesis in ORF AV2 affects viral replication in Mungbean yellow mosaic India virus
Mutation of a mitochondrial outer membrane protein affects chloroplast lipid biosynthesis
Mutations and Deregulation of Ras/Raf/MEK/ERK and PI3K/PTEN/Akt/mTOR Cascades Which Alter Therapy Response.
Mutated KRAS Results in Overexpression of DUSP4, a MAP-Kinase Phosphatase, and SMYD3, a Histone Methyltransferase, in Rectal Carcinomas
Mutagenic Effect of Gold Nanoparticles in the Micronucleus Assay
Mutagenic effects of gold nanoparticles induce aberrant phenotypes in Drosophila melanogaster
Mutation of the cytosolic ribosomal protein-encoding RPS10B gene affects shoot meristematic function in Arabidopsis
Mutation detection in plasmid-based biopharmaceuticals
Mutations of Japanese quail (Coturnix japonica) and recent advances of molecular genetics for this species
Mutations of the TET2 and CBL genes: novel molecular markers in myeloid malignancies
Mutational analysis in BCR-ABL-negative classic myeloproliferative neoplasms: impact on prognosis and therapeutic choices
Mutations in TET2 in myeloid cancers
Mutation in TET2 in Myeloid Cancers
Mutant Huntingtin Impairs Post-Golgi Trafficking to Lysosomes by Delocalizing Optineurin/Rab8 Complex from the Golgi Apparatus
Mutagenesis of Phytophthora infestans for resistance against carboxylic acid amide and phenylamide fungicides
Mutation in mitochondrial DNA as a cause of presbyacusis
Mutagenicity and genotoxicity effects of Lignosus rhinocerotis mushroom mycelium
Mutational Biosynthesis of Ansamitocin Antibiotics: A Diversity-Oriented Approach to Exploit Biosynthetic Flexibility
Mutational and gene expression analysis of mtrDEF, omcA and mtrCAB during arsenate and iron reduction in Shewanella sp ANA-3
Mutation and evolution of microsatellite loci in neurospora
Mutation of Asn28 Disrupts the Dimerization and Enzymatic Activity of SA RS 3CL(pro)
Mutations in type I collagen genes in Japanese osteogenesis imperfecta patients
Mutations in the Ras-Raf Axis Underlie the Prognostic Value of CD133 in Colorectal Cancer
Mutations in Collagen 18A1 (COL18A1) and their relevance to the human phenotype
Mutation of the gene encoding fibrillin-2 results in syndactyly in mice
Mutation in the basolateral secretory Na+-K+-2Cl(-) co-transporter slc12a2 causes deafness and vestibular dysfunction in the mouse
Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness in mice
Mutations of the mouse Twist and sy (Fibrillin 2) genes induced by chemical mutagenesis of ES cells
Mutations in the K+/Cl- cotransporter gene kazachoc (kcc) increase seizure susceptibility in Drosophila
Mutations in the Mitochondrial Methionyl-tRNA Synthetase Cause a Neurodegenerative Phenotype in Flies and a Recessive Ataxia (ARSAL) in Humans
Mutation of the Membrane-Associated M1 Protease APM1 Results in Distinct Embryonic and Seedling Developmental Defects in Arabidopsis
Mutations in cytoplasmic dynein lead to a Huntington's disease-like defect in energy metabolism of brown and white adipose tissues
Mutation analysis of membrane type-1 matrix metalloproteinase (MT1-MMP) - The role of the cytoplasmic tail Cys(574), the active site Glu(240), and furin cleavage motifs in oligomerization, processing, and self-proteolysis of MT1-MMP expressed in breast carcinoma cells
Mutational analysis of the cleavage of the cancer-associated laminin receptor by stromelysin-3 reveals the contribution of flanking sequences to site recognition and cleavage efficiency
Mutagenesis of the DI/DIII Linker in Dengue Virus Envelope Protein Impairs Viral Particle Assembly
Mutational Analysis of the Zippering Reaction during Flavivirus Membrane Fusion
Mutational decay and age of chloroplast and mitochondrial genomes transferred recently to angiosperm nuclear chromosomes
Mutation of the DRY motif reveals different structural requirements for the CC chemokine receptor 5-mediated signaling and receptor endocytosis
Mutations in Two Putative Phosphorylation Motifs in the Tomato Pollen Receptor Kinase LePRK2 Show Antagonistic Effects on Pollen Tube Length
Mutation of Semaphorin-6A Disrupts Limbic and Cortical Connectivity and Models Neurodevelopmental Psychopathology
Mutations in Protocadherin 15 and Cadherin 23 Affect Tip Links and Mechanotransduction in Mammalian Sensory Hair Cells
Mutations within the conserved NS1 nuclear export signal lead to inhibition of influenza A virus replication
Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy
Mutarotation in aqueous solutions of d-levoglucosan: a supramer approach
Mutation-replication statistics of polymerase chain reactions
Mutation in the beta-hairpin of the Bordetella pertussis adenylate cyclase toxin modulates N-lobe conformation in calmodulin
Mutants of phospholipase A (pPLA-I) have a red light and auxin phenotype
Mutations in the NB-ARC domain of I-2 that impair ATP hydrolysis cause autoactivation
Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II
Mutations in AtCML9, a calmodulin-like protein from Arabidopsis thaliana, alter plant responses to abiotic stress and abscisic acid
Mutational dynamics and phylogenetic utility of noncoding chloroplast DNA
Mutation of Conserved Histidines Alters Tertiary Structure and Nanomechanics of Consensus Ankyrin Repeats
Mutational analysis of cis-acting sequences in the 3 '- and 5 '-untranslated regions of RNA2 of red clover necrotic mosaic virus
Mutations in components of antiviral or microbial defense as a basis for breast cancer
Mutation-positive and mutation-negative patients with Cowden and Bannayan-Riley-Ruvalcaba syndromes associated with distinct 10q haplotypes
Mutational Locally Enhanced Sampling (MULES) for quantitative prediction of the effects of mutations at protein-protein interfaces
Mutations in GRIP1 cause Fraser syndrome
Mutation C11994T in the mitochondrial ND4 gene is not a cause of low sperm motility in Portugal
Mutational and structural analyses of the hinge region of membrane type 1-matrix metalloproteinase and enzyme processing
Mutations in a gene encoding a midbody kelch protein in familial and sporadic classical Hodgkin lymphoma lead to binucleated cells
Mutants of neuroserpin that cause dementia accumulate as polymers within the endoplasmic reticulum
Mutational analysis of H3 and H4N termini reveals distinct roles in nuclear import
Mutations in the Cytoplasmic Domain of the Newcastle Disease Virus Fusion Protein Confer Hyperfusogenic Phenotypes Modulating Viral Replication and Pathogenicity
Mutational analysis of the ethylene receptor ETR1. Role of the histidine kinase domain in dominant ethylene insensitivity
Mutational analysis of the PTEN gene in women with premature ovarian failure
Mutation of the highly conserved tryptophan in the serpin breach region alters the inhibitory mechanism of plasminogen activator inhibitor-1
Mutant neuroserpin (S49P) that causes familial encephalopathy with neuroserpin inclusion bodies is a poor proteinase inhibitor and readily forms polymers in vitro
Mutagenesis of the bovSERPINA3-3 demonstrates the requirement of aspartate-371 for intermolecular interaction and formation of dimers
Mutations in the epidermal growth factor receptor gene are linked to smoking-independent, lung adenocarcinoma
Mutations of the epidermal growth factor receptor in non-small cell lung cancer - Search and destroy
Mutations in the Pseudomonas syringae avrRpt2 gene that dissociate its virulence and avirulence activities lead to decreased efficiency in AvrRpt2-induced disappearance of RIN4
Mutation in clp(xoo4158) Reduces Virulence and Resistance to Oxidative Stress in Xanthomonas oryzae pv. oryzae KACC10859
Mutations in the Microtubule-Associated Protein 1A (Map1a) Gene Cause Purkinje Cell Degeneration
Mutation in HSF4 is associated with hereditary cataract in the Australian Shepherd
Mutational Analysis of the Bunyamwera Orthobunyavirus Nucleocapsid Protein Gene
Mutations within the protein Z-dependent protease inhibitor gene are associated with venous thromboembolic disease: a new form of thrombophilia
Mutational analysis of three predicted 5 '-proximal stem-loop structures in the genome of tick-borne encephalitis virus indicates different roles in RNA replication and translation
Mutations in an atypical TIR-NB-LRR-LIM resistance protein confer autoimmunity
Mutations in Fis1 disrupt orderly disposal of defective mitochondria
Mutagenesis and phenotyping resources in zebrafish for studying development and human disease
Mutational Status and Gene Repertoire of IGHV-IGHD-IGHJ Rearrangements in Serbian Patients With Chronic Lymphocytic Leukemia
Mutation spectrum of Drosophila CNVs revealed by breakpoint sequencing
Mutations in single FT- and TFL1-paralogs of rapeseed (Brassica napus L.) and their impact on flowering time and yield components
Mutational Breeding and Genetic Engineering in the Development of High Grain Protein Content
Mutation and evolutionary analyses identify NR2E1-candidate-regulatory mutations in humans with severe cortical malformations
Mutations in a-tubulin confer dinitroaniline resistance at a cost to microtubule function
Mutation-Induced Loop Opening and Energetics for Binding of Tamiflu to Influenza N8 Neuraminidase
Mutations in Sodium Channel beta 1-and beta 2-Subunits Associated With Atrial Fibrillation
Mutations in and near the second calcium-binding domain of integrin alpha IIb affect the structure and function of integrin alpha IIb beta 3
Mutations of an alpha 1,6 Mannosyltransferase Inhibit Endoplasmic Reticulum-Associated Degradation of Defective Brassinosteroid Receptors in Arabidopsis
Mutation screening in the Greek population and evaluation of NLGN3 and NLGN4X genes causal factors for autism
Mutations affecting synaptic levels of neurexin-1 beta in autism and mental retardation
Mutation Rate Evolution in Replicator Dynamics
Mutated beta-catenin evades a microRNA-dependent regulatory loop
Mutation in TERMINAL FLOWER1 Reverses the Photoperiodic Requirement for Flowering in the Wild Strawberry Fragaria vesca
Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot-Marie-Tooth type 2
Mutations in amyloid precursor protein affect its interactions with presenilin/gamma-secretase
Mutational analysis of TRAF6 reveals a conserved functional role of the RING dimerization interface and a potentially necessary but insufficient role of RING-dependent TRAF6 polyubiquitination towards NF-kappa B activation
Mutations in Alstrom protein impair terminal differentiation of cardiomyocytes
Mutation of A677 in histone methyltransferase EZH2 in human B-cell lymphoma promotes hypertrimethylation of histone H3 on lysine 27 (H3K27)
Mutant mouse models of autism spectrum disorders
Mutations in Cog7 affect Golgi structure, meiotic cytokinesis and sperm development during Drosophila spermatogenesis
Mutation analysis of the 8p22 candidate tumor suppressor gene ATIP/MTUS1 in hepatocellular carcinoma
Mutagenicity of water-soluble ZnO nanoparticles in Ames test
Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy
Mutations of the Mouse ELMO Domain Containing 1 Gene (Elmod1) Link Small GTPase Signaling to Actin Cytoskeleton Dynamics in Hair Cell Stereocilia
Mutations in the putative HR-C region of the measles virus F-2 glycoprotein modulate syncytium formation
Mutations and polymorphisms in TP53 gene-an overview on the role in colorectal cancer
Mutation associations in RA-defiant APL
Mutations in the gamma-Secretase Genes NCSTN, PSENEN, and PSEN1 Underlie Rare Forms of Hidradenitis Suppurativa (Acne Inversa)
Mutant DNMT3A: a marker of poor prognosis in acute myeloid leukemia
Mutant DNMT3A: teaming up to transform
Mutations in DNA Methyltransferase (DNMT3A) Observed in Acute Myeloid Leukemia Patients Disrupt Processive Methylation
Mutations of epigenetic regulatory genes are common in thymic carcinomas
Mutated and unmutated chronic lymphocytic leukemia
Mutations in 23S rRNA Confer Resistance against Azithromycin in Pseudomonas aeruginosa
Mutational loss of the prohibitin AtPHB3 results in an extreme constitutive ethylene response phenotype coupled with partial loss of ethylene-inducible gene expression in Arabidopsis seedlings
Mutations in Protein-Binding Hot-Spots on the Hub Protein Smad3 Differentially Affect Its Protein Interactions and Smad3-Regulated Gene Expression
Mutations of the Caenorhabditis elegans brain-specific inorganic phosphate transporter eat-4 affect habituation of the tap-withdrawal response without affecting the response itself
Mutational Landscape of Aggressive Cutaneous Squamous Cell Carcinoma
Mutations in gp120 Contribute to the Resistance of Human Immunodeficiency Virus Type 1 to Membrane-Anchored C-Peptide maC46
Mutations and horizontal transmission have contributed to sulfonamide resistance in Streptococcus pyogenes
Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome
Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype
Mutations in the Transcription Elongation Factor SPT5 Disrupt a Reporter for Dosage Compensation in Drosophila
Mutational Processes Molding the Genomes of 21 Breast Cancers
Mutational analysis of the tyrosine kinome in serous and clear cell endometrial cancer uncovers rare somatic mutations in TNK2 and DDR1
Mutational signatures: the patterns of somatic mutations hidden in cancer genomes
Mutants, Overexpressors, and Interactors of Arabidopsis Plastocyanin Isoforms: Revised Roles of Plastocyanin in Photosynthetic Electron Flow and Thylakoid Redox State
Mutations in NFKB2 and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficiencies
Mutational and biochemical analysis of the DNA-entry nuclease EndA from Streptococcus pneumoniae
Mutants of plant genes for developing cancer vaccines
Mutations in ERK2 binding sites affect nuclear entry
Mutation analysis for DJ-1 in sporadic and familial parkinsonism: Screening strategy in parkinsonism
Mutations in the shutter region of antithrombin result in formation of disulfide-linked dimers and severe venous thrombosis
Mutant onco-proteins as drug targets: successes, failures, and future prospects
Mutant PIK3CA controls DUSP1-dependent ERK 1/2 activity to confer response to AKT target therapy
Mutating Conserved Cysteines in the Alphavirus E2 Glycoprotein Causes Virus-Specific Assembly Defects
Mutant huntingtin impairs the post-Golgi trafficking of brain-derived neurotrophic factor but not its Val66Met polymorphism
Mutation screen of the TUB gene in patients with retinitis pigmentosa and Leber congenital amaurosis
Mutations in the intersubunit bridge regions of 23 S rRNA
Mutational analysis of nocK and nocL in the nocardicin A producer Nocardia uniformis
Mutations in the Prostaglandin Transporter SLCO2A1 Cause Primary Hypertrophic Osteoarthropathy with Digital Clubbing
Mutational Analysis of the High-Affinity Zinc Binding Site Validates a Refined Human Dopamine Transporter Homology Model
Mutagenesis of the thiostrepton precursor peptide at Thr7 impacts both biosynthesis and function
Mutational Analysis of the Thienamycin Biosynthetic Gene Cluster from Streptomyces cattleya
Mutagenesis of subunit N of the Escherichia coli complex I. Identification of the initiation codon and the sensitivity of mutants to decylubiquinone
Mutant p53 is a transcriptional co-factor that binds to G-rich regulatory regions of active genes and generates transcriptional plasticity
Mutation I810N in the alpha 3 isoform of Na+,K+-ATPase causes impairments in the sodium pump and hyperexcitability in the CNS
Mutation of Mapped TIA-1/TIAR Binding Sites in the 3 ' Terminal Stem-Loop of West Nile Virus Minus-Strand RNA in an Infectious Clone Negatively Affects Genomic RNA Amplification
Mutations in yeast ARV1 alter intracellular sterol distribution and are complemented by human ARV1
Mutations in erg4 affect the sensitivity of Saccharomyces cerevisiae to medium-chain fatty acids
Mutations in an amino acid transporter gene are responsible for sex-linked translucent larval skin of the silkworm, Bombyx mori
Mutations in viral movement protein alter systemic infection and identify an intercellular barrier to entry into the phloem long-distance transport system
Mutations in herpes simplex virus gD protein affect receptor binding by different molecular mechanisms
Mutation of the maturase lipoprotein attenuates the virulence of Streptococcus equi to a greater extent than does loss of general lipoprotein lipidation
Mutations in eukaryotic release factors 1 and 3 act as general nonsense suppressors in Drosophila
Mutations in Flavobacterium johnsoniae sprE Result in Defects in Gliding Motility and Protein Secretion
Mutational analysis of the-10 region from the Mycobacterium tuberculosis lipF promoter
Mutational analysis of conserved glutamic acids of Pho89, a Saccharomyces cerevisiae high-affinity inorganic phosphate:Na+ symporter
Mutational analysis of conserved regions harboring catalytic triad residues of the levansucrase protein encoded by the lsc-3 gene ( lsc3) of Pseudomonas syringae pv. tomato DC3000
Mutations in lipopolysaccharide biosynthetic genes impair maize rhizosphere and root colonization of Rhizobium tropici CIAT899
Mutation in the SH1 helix reduces the activation energy of the ATP-induced conformational transition of myosin
Mutating the Converter-Relay Interface of Drosophila Myosin Perturbs ATPase Activity, Actin Motility, Myofibril Stability and Flight Ability
Mutation in E1, the Ubiquitin Activating Enzyme, Reduces Drosophila Lifespan and Results in Motor Impairment
Mutagenesis studies toward understanding the intracellular signaling mechanism of antithrombin
Mutations in mammalian tolloid-like 1 gene detected in adult patients with ASD
Mutagenesis of the dengue virus type 2 NS5 methyltransferase domain
Mutated K-ras activates CDK8 to stimulate the epithelial-to-mesenchymal transition in pancreatic cancer in part via the Wnt/beta-catenin signaling pathway
Mutational analysis of ABCC8, KCNJ11, GLUD1, HNF4A and GCK genes in 30 Chinese patients with congenital hyperinsulinism
Mutation analysis of the ATP2A2 gene in Chinese patients with Darier's disease
Mutations in MAPT give rise to aneuploidy in animal models of tauopathy
Mutant p62(P392L) Stimulation of Osteoclast Differentiation in Paget's Disease of Bone
Mutation spectrum and inhibitor risk in 100 Korean patients with severe haemophilia A
Mutational and Metal Binding Analysis of the Endonuclease Domain of the Influenza Virus Polymerase PA Subunit
Mutational Analyses of the Influenza A Virus Polymerase Subunit PA Reveal Distinct Functions Related and Unrelated to RNA Polymerase Activity
Mutant USA strain of porcine circovirus type 2 (mPCV2) exhibits similar virulence to the classical PCV2a and PCV2b strains in caesarean-derived, colostrum-deprived pigs
Mutation Studies in Ascidians: A Review
Mutations in PRDM5 in Brittle Cornea Syndrome Identify a Pathway Regulating Extracellular Matrix Development and Maintenance
Mutations in the Arabidopsis H3K4me2/3 Demethylase JMJ14 Suppress Posttranscriptional Gene Silencing by Decreasing Transgene Transcription
Mutational Analysis of Sulfite Reductase Hemoprotein Reveals the Mechanism for Coordinated Electron and Proton Transfer
Mutational landscape of intrahepatic cholangiocarcinoma
Mutant K-Ras increases GSK-3 beta gene expression via an ETS-p300 transcriptional complex in pancreatic cancer
Mutagenicity, antimutagenicity and cytotoxicity evaluation of South African Podocarpus species
Mutation Screening in Candidate Genes in Four Chinese Brachydactyly Families
Mutations with pathogenic potential in proteins located in or at the composite junctions of the intercalated disk connecting mammalian cardiomyocytes: a reference thesaurus for arrhythmogenic cardiomyopathies and for Naxos and Carvajal diseases
Mutagenicity and anti-mutagenicity of Acanthopanax divaricatus var. albeofructus
Mutations in CIC and IDH1 cooperatively regulate 2-hydroxyglutarate levels and cell clonogenicity
Mutagenicity and Genotoxicity of Water Treated for Human Consumption Induced by Chlorination By-products
Mutational characterization of individual breast tumors: TP53 and PI3K pathway genes are frequently and distinctively mutated in different subtypes
Mutations in NALCN Cause an Autosomal-Recessive Syndrome with Severe Hypotonia, Speech Impairment, and Cognitive Delay
Mutant Metabolic Enzymes Are at the Origin of Gliomas
Mutant IDH1 Confers an in Vivo Growth in a Melanoma Cell Line with BRAF Mutation
Mutations of isocitrate dehydrogenase 1 and 2 in intrahepatic cholangiocarcinoma
Mutant IDH1-Driven Cellular Transformation Increases RAD51-Mediated Homologous Recombination and Temozolomide Resistance
Mutational loss of Arabidopsis SLOW WALKER2 results in reduced endogenous spermine concomitant with increased aluminum sensitivity
Mutant p53 Reprograms TNF Signaling in Cancer Cells through Interaction with the Tumor Suppressor DAB2IP
Mutation scanning using high-resolution melting
Mutation (variation) databases and registries: a rationale for coordination of efforts
Mutation pattern of KRAS and BRAF oncogenes in colorectal cancer patients
Mutation analysis of the motor neuron and pancreas homeobox 1 (MNX1, former HLXB9) gene in Swedish patients with Currarino syndrome
Mutations in Zebrafish lrp2 Result in Adult-Onset Ocular Pathogenesis That Models Myopia and Other Risk Factors for Glaucoma
Mutagenesis of Zinc Ligand Residue Cys221 Reveals Plasticity in the IMP-1 Metallo-beta-Lactamase Active Site
Mutations in the BRCT binding site of BRCA1 result in hyper-recombination
Mutations in genes involved in nonsense mediated decay ameliorate the phenotype of sel-12 mutants with amber stop mutations in Caenorhabditis elegans
Mutant SOD1 in neuronal mitochondria causes toxicity and mitochondrial dynamics abnormalities
Mutation in the Tight-Junction Gene Claudin 19 (CLDN19) and Familial Hypomagnesemia, Hypercalciuria, Nephrocalcinosis (FHHNC) and Severe Ocular Disease
Mutation rates in Scots pine (Pinus sylvestris L.) from the Chernobyl exclusion zone evaluated with amplified fragment-length polymorphisms (AFLPs) and microsatellite markers
Mutated IDH1 Is a Favorable Prognostic Factor for Type 2 Gliomatosis Cerebri
Mutagenic effect, antioxidant and anticancer activities of six medicinal plants from Burkina Faso
Mutation-Rate Threshold under Changing Environments with Sharp-Peak Fitness Function
Mutation analysis of hepatitis B virus reverse transcriptase region among untreated chronically infected patients in Ahvaz city (South-West of Iran)
Mutations in NLRP7 are associated with diploid biparental hydatidiform moles, but not androgenetic complete moles
Mutations in the Human naked cuticle Homolog NKD1 Found in Colorectal Cancer Alter Wnt/Dvl/beta-Catenin Signaling
Mutation of a self-processing site in caspase-8 compromises its apoptotic but not its nonapoptotic functions in bacterial artificial chromosome-transgenic mice
Mutations Causing Familial Biparental Hydatidiform Mole Implicate C6orf221 as a Possible Regulator of Genomic Imprinting in the Human Oocyte
Mutations of the synapse genes and intellectual disability syndromes
Mutations in chronic lymphocytic leukemia and how they affect therapy choice: focus on NOTCH1, SF3B1, and TP53
Mutations in genes involved in splicing in human malignancies
Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis
Mutations in RNA Splicing Machinery in Human Cancers
Mutational spectrum analysis of chronic myelomonocytic leukemia includes genes associated with epigenetic regulation: UTX, EZH2, and DNMT3A
Mutations to metabolic enzymes in cancer herald a need to unify genetics and biochemistry
Mutant IDH1 is required for IDH1 mutated tumor cell growth
Mutant IDH1 Enhances the Production of 2-Hydroxyglutarate Due to Its Kinetic Mechanism
Mutant IDH is sufficient to initiate enchondromatosis in mice
Mutational spectrum defines primary and secondary myelofibrosis
Mutational profiling in patients with MDS: Ready for every-day use in the clinic?
Mutational analysis of RNA splicing machinery components in 206 children with myeloid malignancies
Mutations affecting mRNAsplicing define distinct clinical phenotypes and correlate with patient outcome in myelodysplastic syndromes
Mutational analysis of therapy-related myelodysplastic syndromes and acute myelogenous leukemia
Mutation of a cleavage site adjacent to the mature domain leads to increase in secreted mature BMP-2 with reduced activity
Mutation in the S3 segment of KCNQ1 results in familial lone atrial fibrillation
Mutations in sodium channel beta-subunit SCN3B are associated with early-onset lone atrial fibrillation
Mutational analysis of the PITX2 and NKX2-5 genes in patients with idiopathic atrial fibrillation
Mutations in the epidermal growth factor receptor gene in non-small cell lung cancer: Impact on treatment beyond gefitinib and erlotinib
Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of alpha-dystroglycan
Mutations of Helicobacter pylori Associated with Fluoroquinolone Resistance in Korea
Mutation analysis of Rad18 in human cancer cell lines and non small cell lung cancer tissues
Mutations Associated With the Therapeutic Efficacy of Adefovir Dipivoxil Added to Lamivudine in Patients Resistant to Lamivudine With Type B Chronic Hepatitis
Mutation and selection of Oenococcus oeni for controlling wine malolactic fermentation
Mutations in the P-Type Cation-Transporter ATPase 4, PfATP4, Mediate Resistance to Both Aminopyrazole and Spiroindolone Antimalarials
Mutational status of VHL gene and its clinical importance in renal clear cell carcinoma
Mutation of the receptor tyrosine phosphatase PTPRC (CD45) in T-cell acute lymphoblastic leukemia
Mutant hypoxia-inducible factor la modified bone marrow mesenchymal stem cells ameliorate cerebral ischemia
Mutations of the Apolipoprotein A5 Gene with Inherited Hypertriglyceridaemia: Review of the Current Literature
Mutational screening of CYP1B1 in Turkish PCG families and functional analyses of newly detected mutations
Mutations in DNAJC5, Encoding Cysteine-String Protein Alpha, Cause Autosomal-Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis
Mutations in the Gene DNAJC5 Cause Autosomal Dominant Kufs Disease in a Proportion of Cases: Study of the Parry Family and 8 Other Families
Mutation of the CLN6 Gene in Teenage-Onset Progressive Myoclonus Epilepsy
Mutagenesis and Functional Studies with Succinate Dehydrogenase Inhibitors in the Wheat Pathogen Mycosphaerella graminicola
Mutations in non-structural 5A and rapid viral response to pegylated interferon-alpha-2b plus ribavirin therapy are associated with therapeutic efficacy in patients with genotype 1b chronic hepatitis C
Mutagenicity and Antimutagenicity of Hydrophilic and Lipophilic Extracts of Thai Northern Purple Rice
Mutations in PLK4, encoding a master regulator of centriole biogenesis, cause microcephaly, growth failure and retinopathy
Mutants of GABA Transaminase (POP2) Suppress the Severe Phenotype of succinic semialdehyde dehydrogenase (ssadh) Mutants in Arabidopsis
Mutations in the Reverse Transcriptase and Protease Genes of Human Immunodeficiency Virus-1 from Antiretroviral Naive and Treated Pediatric Patients
Mutagenic and physiological responses in the juveniles of African catfish, Clarias gariepinus (Burchell 1822) following short term exposure to praziquantel
Mutations in C5ORF42 Cause Joubert Syndrome in the French Canadian Population
Mutations in TMEM231 cause Joubert syndrome in French Canadians
Mutations in Two Independent Pathways Are Sufficient to Create Hermaphroditic Nematodes
Mutations, structural variations, and genome-wide resequencing: Where to from here in our understanding of disease and evolution?
Mutant SOD1 and Mitochondrial Damage Alter Expression and Splicing of Genes Controlling Neuritogenesis in Models of Neurodegeneration
Mutation Altering the miR-184 Seed Region Causes Familial Keratoconus with Cataract
Mutations in KAT6B, Encoding a Histone Acetyltransferase, Cause Genitopatellar Syndrome
Mutation in GATA2 linked to leukemia predisposition
Mutational spectrum of myeloid malignancies with inv(3)/t(3;3) reveals a predominant involvement of RAS/RTK signaling pathways
Mutational approach for enhancement of artemisinin in Artemisia annua
Mutation analysis in Saudi Duchenne and Becker muscular dystrophy patients using multiplex PCR
Mutational analysis of the BRAF, RAS and EGFR genes in human adrenocortical carcinomas
Mutant K-ras promotes carcinogen-induced murine colorectal tumourigenesis, but does not alter tumour chromosome stability
Mutant p53 in Cancer: New Functions and Therapeutic Opportunities
Mutations in FGFR3 and PIK3CA, singly or combined with RAS and AKT1, are associated with AKT but not with MAPK pathway activation in urothelial bladder cancer
Mutations in the focal adhesion targeting region of deleted in liver cancer-1 attenuate their expression and function
Mutations, Clinical Findings and Survival Estimates in South American Patients with X-Linked Adrenoleukodystrophy
Mutations of the TP53 gene in adenocarcinoma and squamous cell carcinoma of the cervix: A systematic review
Mutations in KATNB1 Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural Progenitors
Mutations in PRKN and SNCA Genes Important for the Progress of Parkinson's Disease
Mutagenic impact on fish of runoff events in agricultural areas in south-west France
Mutational Analysis of Cysteine Residues of the Insect Odorant Co-receptor (Orco) from Drosophila melanogaster Reveals Differential Effects on Agonist-and Odorant-tuning Receptor-dependent Activation
Mutational Analysis of Methyl-CpG Binding Protein 2 (MECP2) Gene in Indian Cases of Rett Syndrome
Mutations in EZH2 Cause Weaver Syndrome
Mutational analysis of the Ras converting enzyme reveals a requirement for glutamate and histidine residues
Mutation of PPP2R1A: a new clue in unveiling the pathogenesis of uterine serous carcinoma
Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
Mutation of RNA Polymerase beta Subunit (rpoB) Promotes hVISA-to-VISA Phenotypic Conversion of Strain Mu3
Mutation in Elongation Factor G Confers Resistance to the Antibiotic Argyrin in the Opportunistic Pathogen Pseudomonas aeruginosa
Mutant copper-zinc superoxide dismutase associated with amyotrophic lateral sclerosis binds to adenine/uridine-rich stability elements in the vascular endothelial growth factor 3'-untranslated region
Mutational Spectrum of the NKX2-5 Gene in Patients with Lone Atrial Fibrillation
Mutational analysis of primary central nervous system lymphoma
Mutation of Dcdc2 in mice leads to impairments in auditory processing and memory ability
Mutation of the dyslexia-associated gene Dcdc2 impairs LTM and visuo-spatial performance in mice
Mutation Rates and Evolution of Multiple Coding in RNA-based Protocells
Mutations of the Gene Encoding Otogelin Are a Cause of Autosomal-Recessive Nonsyndromic Moderate Hearing Impairment
Mutations in the IrpE gene of Ralstonia solanacearum affects Hrp Pili production and virulence
Mutant polycystin-2 induces proliferation in primary rat tubular epithelial cells in a STAT-1/p21-independent fashion accompanied instead by alterations in expression of p57(KIP2) and Cdk2
Mutant mice with small amounts of BubR1 display accelerated age-related gliosis
Mutations in the alpha-helical region of the amino terminus of the Maize rayado fino virus capsid protein and CP:RNA ratios affect virus-like particle encapsidation of RNAs
Mutation scanning-coupled tools for the analysis of genetic variation in Taenia and diagnosis - Status and prospects
Mutations to A/Puerto Rico/8/34 PB1 gene improves seasonal reassortant influenza A virus growth kinetics
Mutation screening of the PCDH15 gene in Spanish patients with Usher syndrome type I
Mutations and non-inferiority analyses show a way forward
Mutation of the GABA receptor associated with fipronil resistance in the whitebacked planthopper, Sogatella furcifera
Mutations in TRPV4 cause an inherited arthropathy of hands and feet
Mutational Analysis of the Control Cable That Mediates Transmembrane Signaling in the Escherichia coli Serine Chemoreceptor
Mutations of the epigenetics-modifying gene (DNMT3a, TET2, IDH1/2) at diagnosis may induce FLT3-ITD at relapse in de novo acute myeloid leukemia
Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis
Mutation risk associated with paternal and maternal age in a cohort of retinoblastoma survivors
Mutant huntingtin, abnormal mitochondrial dynamics, defective axonal transport of mitochondria, and selective synaptic degeneration in Huntington%26apos;s disease
Mutations in the INF2 gene account for a significant proportion of familial but not sporadic focal and segmental glomerulosclerosis
Mutations in NMNAT1 cause Leber congenital amaurosis with early-onset severe macular and optic atrophy
Mutations in the voltage-gated sodium channel gene of anophelines and their association with resistance to pyrethroids - a review
Mutations in mitochondrial DNA and approaches for their correction
Mutations in the essential FAS II beta-hydroxyacyl ACP dehydratase complex confer resistance to thiacetazone in Mycobacterium tuberculosis and Mycobacterium kansasii
Mutations in mitochondrial DNA polymerase-gamma promote breast tumorigenesis
Mutagenesis of barley malting quality QTLs with Ds transposons
Mutation Update for GNE Gene Variants Associated with GNE Myopathy
Mutations in the two ribosomal RNA genes in mitochondrial DNA among Finnish children with hearing impairment
Mutational analysis of genes coding for cell surface proteins in colorectal cancer cell lines reveal novel altered pathways, druggable mutations and mutated epitopes for targeted therapy
Mutation analysis and characterization of HSD17B2 sequence variants in breast cancer cases from French Canadian families with high risk of breast and ovarian cancer
Mutation in the CPC motif-containing 6th transmembrane domain affects intracellular localization, trafficking and copper transport efficiency of ATP7A protein in mosaic mutant mice-an animal model of Menkes disease
Mutations in BRIP1 confer high risk of ovarian cancer
Mutagenesis and Molecular Modeling of the Orthosteric Binding Site of the mGlu2 Receptor Determining Interactions of the Group II Receptor Antagonist H-3-HYDIA
Mutations of neuraminidase implicated in neuraminidase inhibitors resistance
Mutations to the Formin Homology 2 Domain of INF2 Protein Have Unexpected Effects on Actin Polymerization and Severing
Mutational and Phylogenetic Analyses of the Mycobacterial mbt Gene Cluster
Mutation symmetries in BPS quiver theories: building the BPS spectra
Mutants strike again in APL
Mutations in Critical Domains Confer the Human mTOR Gene Strong Tumorigenicity
Mutations in NOTCH2 in Families with Hajdu-Cheney Syndrome
Mutations in IL36RN/IL1F5 Are Associated with the Severe Episodic Inflammatory Skin Disease Known as Generalized Pustular Psoriasis
Mutation in Torenia fournieri Lind. UFO homolog confers loss of TfLFY interaction and results in a petal to sepal transformation
Mutation in aging mice occurs in diverse cell types that proliferate postmutation
Mutational Analysis and Modeling Reveal Functionally Critical Residues in Transmembrane Segments 1 and 3 of the UapA Transporter
Mutational Landscape of Basal Cell Carcinomas by Whole-Exome Sequencing
Mutations in two non-canonical Arabidopsis SWI2/SNF2 chromatin remodeling ATPases cause embryogenesis and stem cell maintenance defects
Mutational analysis of positively charged amino acid residues of Uukuniemi phlebovirus nucleocapsid protein
Mutation in collagen-I that confers resistance to the action of collagenase results in failure of recovery from CCl4-induced liver fibrosis, persistence of activated hepatic stellate cells, and diminished hepatocyte regeneration
Mutations in two matrix metalloproteinase genes, MMP-2 and MT1-MMP, are synthetic lethal in mice
Mutation of Membrane Type-1 Metalloproteinase, MT1-MMP, Causes the Multicentric Osteolysis and Arthritis Disease Winchester Syndrome
Mutant LRRK2 Elicits Calcium Imbalance and Depletion of Dendritic Mitochondria in Neurons
Mutations of noncollagen genes in osteogenesis imperfecta - implications of the gene products in collagen biosynthesis and pathogenesis of disease
Mutations in the M-Gene Segment Can Substantially Increase Replication Efficiency of NS1 Deletion Influenza A Virus in MDCK Cells
Mutation in TAGAP Is Protective of Anal Sepsis in Ileocolic Crohn's Disease
Mutational and expressional analyses if NRF2 and KEAP1 in sarcomas
Mutations in the pncA and rpsA genes among 77 Mycobacterium tuberculosis isolates in Kazakhstan
Mutation of OPA1 gene causes deafness by affecting function of auditory nerve terminals
Mutations in the mitochondrial complex I assembly factor NDUFAF1 cause fatal infantile hypertrophic cardiomyopathy
Mutant Cbl proteins as oncogenic drivers in myeloproliferative disorders
Mutant Forkhead L2 (FOXL2) Proteins Associated with Premature Ovarian Failure (POF) Dimerize with Wild-Type FOXL2, Leading to Altered Regulation of Genes Associated with Granulosa Cell Differentiation
Mutations in the TGF-beta repressor SKI cause Shprintzen-Goldberg syndrome with aortic aneurysm
Mutations in the GlyT2 Gene (SLC6A5) Are a Second Major Cause of Startle Disease
Mutations in the GM1 Binding Site of Simian Virus 40 VP1 Alter Receptor Usage and Cell Tropism
Mutations in the ABCA3 Gene Are Associated With Cataract-Microcornea Syndrome
Mutations in the pre-replication complex cause Meier-Gorlin syndrome
Mutation in PLK4, encoding a master regulator of centriole formation, defines a novel locus for primordial dwarfism
Mutation and genomic amplification of the PIK3CA proto-oncogene in pituitary adenomas
Mutations in a P-Type ATPase Gene Cause Axonal Degeneration
Mutational Analysis of Circulating Tumor Cells from Colorectal Cancer Patients and Correlation with Primary Tumor Tissue
Mutant PKC gamma in Spinocerebellar Ataxia Type 14 Disrupts Synapse Elimination and Long-Term Depression in Purkinje Cells In Vivo
Mutant beta-III Spectrin Causes mGluR1 alpha Mislocalization and Functional Deficits in a Mouse Model of Spinocerebellar Ataxia Type 5
Mutant huntingtin alters Tau phosphorylation and subcellular distribution
Mutation in PHC1 implicates chromatin remodeling in primary microcephaly pathogenesis
Mutations in WDR62, encoding a centrosomal and nuclear protein, in Indian primary microcephaly families with cortical malformations
Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis
Mutational analysis of familial and sporadic amyotrophic lateral sclerosis with OPTN mutations in Japanese population
Mutations in UBQLN2 are rare in French amyotrophic lateral sclerosis
Mutations of p53 and KRAS activate NF-kappa B to promote chemoresistance and tumorigenesis via dysregulation of cell cycle and suppression of apoptosis in lung cancer cells
Mutations in DDHD2, Encoding an Intracellular Phospholipase A(1), Cause a Recessive Form of Complex Hereditary Spastic Paraplegia
Mutation in TECPR2 Reveals a Role for Autophagy in Hereditary Spastic Paraparesis
Mutational Landscape of the Essential Autophagy Gene BECN1 in Human Cancers
Mutations in SERPINF1 Cause Osteogenesis Imperfecta Type VI
Mutations in FKBP10 can cause a severe form of isolated Osteogenesis imperfecta
Mutations in PLOD2 Cause Autosomal-Recessive Connective Tissue Disorders Within the Bruck Syndrome-Osteogenesis Imperfecta Phenotypic Spectrum
Mutagenic potential of the isoflavone irilone in cultured V79 cells
Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome
Mutations in mitochondrial ribosomal protein MRPL12 leads to growth retardation, neurological deterioration and mitochondrial translation deficiency
Mutagenesis of Trichoderma reesei endoglucanase I: impact of expression host on activity and stability at elevated temperatures
Mutations and chromosomal rearrangements of JAK2: not only a myeloid issue
Mutational Status of the TP53 Gene As a Predictor of Response and Survival in Patients With Chronic Lymphocytic Leukemia: Results From the LRF CLL4 Trial
Mutations in the prostaglandin transporter encoding gene SLCO2A1 Cause primary hypertrophic osteoarthropathy and isolated digital clubbing
Mutational analysis of a predicted double -propeller domain of the DspA/E effector of Erwinia amylovora
Mutation Screening of the APOA5 Gene in Subjects With Coronary Artery Disease
Mutation screening of the DYT6/THAP1 gene in Serbian patients with primary dystonia
Mutation of Arabidopsis SPLICEOSOMAL TIMEKEEPER LOCUS1 Causes Circadian Clock Defects
Mutation profile of the GNE gene in Japanese patients with distal myopathy with rimmed vacuoles (GNE myopathy)
Mutations affecting interaction of integrase with TNPO3 do not prevent HIV-1 cDNA nuclear import
Mutagenicity assessment of aerosols in emissions from wood combustion in Portugal
Mutant Twinkle increases dopaminergic neurodegeneration, mtDNA deletions and modulates Parkin expression
Mutations in ANO3 Cause Dominant Craniocervical Dystonia: Ion Channel Implicated in Pathogenesis
Mutation of Three Residues in the Third Intracellular Loop of the Dopamine D-2 Receptor Creates an Internalization-defective Receptor
Mutations of DEPDC5 cause autosomal dominant focal epilepsies
Mutation analysis of RAD51D in non-BRCA1/2 ovarian and breast cancer families
Mutagenicity and clastogenicity of native airborne particulate matter samples collected under industrial, urban or rural influence
Mutational and expressional analyses of MYD88 gene in common solid cancers
Mutation in the abcb7 gene causes abnormal iron and fatty acid metabolism in developing medaka fish
Mutations in an Arabidopsis Mitochondrial Transcription Termination Factor-Related Protein Enhance Thermotolerance in the Absence of the Major Molecular Chaperone HSP101
Mutation of the Zebrafish Nucleoporin elys Sensitizes Tissue Progenitors to Replication Stress
Mutagenesis in Bacterial Spores Exposed to Space and Simulated Martian Conditions: Data from the EXPOSE-E Spaceflight Experiment PROTECT
Mutation analysis of BRAF and KIT in circulating melanoma cells at the single cell level
Mutation Patterns of 16 Genes in Primary and Secondary Acute Myeloid Leukemia (AML) with Normal Cytogenetics
Mutagenicity and antimutagenicity of (-)-hinokinin a trypanosomicidal compound measured by Salmonella microsome and comet assays
Mutations in SLC2A2 Gene Reveal hGLUT2 Function in Pancreatic beta Cell Development
Mutations in the Mevalonate Kinase (MVK) Gene Cause Nonsyndromic Retinitis Pigmentosa
Mutant p53 Disrupts MCF-10A Cell Polarity in Three-dimensional Culture via Epithelial-to-mesenchymal Transitions
Mutations Conferring Resistance to Viral DNA Polymerase Inhibitors in Camelpox Virus Give Different Drug-Susceptibility Profiles in Vaccinia Virus
Mutations in the Fusion Protein Cleavage Site of Avian Paramyxovirus Serotype 2 Increase Cleavability and Syncytium Formation but Do Not Increase Viral Virulence in Chickens
Mutation of the F-Protein Cleavage Site of Avian Paramyxovirus Type 7 Results in Furin Cleavage, Fusion Promotion, and Increased Replication In Vitro but Not Increased Replication, Tissue Tropism, or Virulence in Chickens
Mutations in SLC33A1 Cause a Lethal Autosomal-Recessive Disorder with Congenital Cataracts, Hearing Loss, and Low Serum Copper and Ceruloplasmin
Mutations in the beta-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities
Mutant p53 Disrupts the Stress MAPK Activation Circuit Induced by ASK1-Dependent Stabilization of Daxx
Mutations in the phosphatidylinositol 3-kinase pathway: role in tumor progression and therapeutic implications in breast cancer
Mutagens interfere with microRNA maturation by inhibiting DICER. An in silico biology analysis
Mutant TP53 Posttranslational Modifications: Challenges and Opportunities
Mutation in the SLC29A3 Gene: A New Cause of a Monogenic, Autoinflammatory Condition
Mutations in the SASPase Gene (ASPRV1) Are Not Associated with Atopic Eczema or Clinically Dry Skin
Mutational analysis and genotype-phenotype correlations in southern Indian patients with sporadic and familial aniridia
Mutational Screening of LCA Genes Emphasizing RPE65 in South Indian Cohort of Patients
Mutant allele frequency predicts the efficacy of EGFR-TKIs in lung adenocarcinoma harboring the L858R mutation
Mutation of a U2 snRNA Gene Causes Global Disruption of Alternative Splicing and Neurodegeneration
Mutations in SNRPB, Encoding Components of the Core Splicing Machinery, Cause Cerebro-Costo-Mandibular Syndrome
Mutations in the GW-repeat protein SUO reveal a developmental function for microRNA-mediated translational repression in Arabidopsis
Mutations associated with occult hepatitis B virus infection result in decreased surface antigen expression in vitro
Mutations in Bacchus reveal a tyramine-dependent nuclear regulator for acute ethanol sensitivity in Drosophila
Mutational analysis of the neurexin/neuroligin complex reveals essential and regulatory components
Mutations in alternative carbon utilization pathways in Candida albicans attenuate virulence and confer pleiotropic phenotypes
Mutational Spectrum of Semaphorin 3A and Semaphorin 3D Genes in Spanish Hirschsprung patients
Mutation analysis of SMAD2, SMAD3, and SMAD4 genes in hereditary non-polyposis colorectal cancer
Mutational analysis of Smad3, a candidate tumor suppressor implicated in TGF-beta and menin pathways, in parathyroid adenomas and enteropancreatic endocrine tumors
Mutations in the Gene Encoding DMT1: Clinical Presentation Treatment
Mutation of putative branchpoint consensus sequences in plant introns reduces splicing efficiency
Mutational analysis of the U12-dependent branch site consensus sequence
Mutations of TP53 do not correlate with the sensitivity to paclitaxel - a study using 27 gynaecological cancer cell lines
Mutational hotspots in the p53 gene revealed by classification analysis
Mutational spectrum induced by acetaldehyde in the HPRT gene of human T lymphocytes resembles that in the p53 gene of esophageal cancers
Mutation rate and predicted phenotypic target sizes in ethylnitrosourea-treated mice
Mutation hotspots in the p53 gene in tumors of different origin: correlation with evolutionary conservation and signs of positive selection
Mutational biases associated with potential iron-binding DNA motifs in rodent lacI and human p53 mutational databases
Mutant p53 and aberrant cytosine methylation cooperate to silence gene expression
Mutagenesis and carcinogenesis caused by the oxidation of nucleic acids
Mutation of Drosophila homer disrupts control of locomotor activity and behavioral plasticity
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
Mutation screening and association study of the candidate prostate cancer susceptibility genes MSR1, PTEN, and KLF6
Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome
Mutations in the Hedgehog Pathway Genes SMO and PTCH1 in Human Gastric Tumors
Mutagenesis by transient misalignment in the human mitochondrial DNA control region
Mutations of NFKBIA, encoding I kappa B alpha, are a recurrent finding in classical Hodgkin lymphoma but are not a unifying feature of non-EBV-associated cases
Mutational and inhibitive analysis of SARS coronavirus 3C-like protease by fluorescence resonance energy transfer-based assays
Mutagenesis of the murine hepatitis virus nsp1-coding region identifies residues important for protein processing, viral RNA synthesis, and viral replication
Mutational specificity of gamma-radiation-induced guanine-thymine and thymine-guanine intrastrand cross-links in mammalian cells and translesion synthesis past the guanine-thymine lesion by human DNA polymerase eta
Mutations of human TMHS cause recessively inherited non-syndromic hearing loss
Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss
Mutagenesis of pairwise combinations of histone amino-terminal tails reveals functional redundancy in budding yeast
Mutational Analysis of the Class IIa Bacteriocin Curvacin A and Its Orientation in Target Cell Membranes
Mutational Analysis of Residues in the Helical Region of the Class IIa Bacteriocin Pediocin PA-1
Mutation Screening of Multiple Genes in Spanish Patients with Autosomal Recessive Retinitis Pigmentosa by Targeted Resequencing
Mutagenesis in the alpha 3 alpha 4 GyrA helix and in the toprim domain of GyrB refines the contribution of Mycobacterium tuberculosis DNA gyrase to intrinsic resistance to Quinolones
Mutations in STIL, Encoding a Pericentriolar and Centrosomal Protein, Cause Primary Microcephaly
Mutational comparison of the single-domained APOBEC3C and double-domained APOBEC3F/G anti-retroviral cytidine deaminases provides insight into their DNA target site specificities
Mutation in ace1 associated with an insecticide resistant population of Plutella xylostella
Mutations causing defects in the biosynthesis and response to gibberellins, abscisic acid and phytochrome B do not inhibit vernalization in Arabidopsis fca-1
Mutational analysis of steroidogenic factor 1 (NR5a1) in 24 boys with bilateral anorchia: a French collaborative study
Mutator-Like Elements with Multiple Long Terminal Inverted Repeats in Plants
Mutation rates in the dystrophin gene: A hotspot of mutation at a CpG dinucleotlide
Mutability in the Matrix Gene of Novel Influenza A H1N1 Virus Detected Using a FRET Probe-Based Real-Time Reverse Transcriptase PCR Assay
Mutations in the mitochondrial tRNA(Ser(AGY)) gene are associated with deafness, retinal degeneration, myopathy and epilepsy
Mutant A1555G Mitochondrial 12S rRNA and Aminoglycoside Susceptibility Reply
Mutational uncoupling of alpha(1A)-adrenergic receptors from G proteins also uncouples mitogenic and transcriptional responses in PC12 cells
Mutation screening of the Homer gene family and association analysis in schizophrenia
Mutagenic properties of PM2.5 air pollution in the Padana Plain (Italy) before and in the course of XX Winter Olympic Games of "Torino 2006"
Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families
Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment (vol 20, pg 370, 1998)
Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region
Mutations in connexin 32: the molecular and biophysical bases for the X-linked form of Charcot-Marie-Tooth disease
Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss
Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29
Mutations in GJB6 cause hidrotic ectodermal dysplasia
Mutations in the second extracellular region of connexin 43 prevent localization to the plasma membrane, but do not affect its ability to suppress cell growth
Mutations in the gene for connexin 26 (GJB2) that cause hearing loss have a dominant negative effect on connexin 30
Mutation analysis of Connexin 31 (GJB3) in sporadic non-syndromic hearing impairment
Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28
Mutant ICR mouse, kuru(2), manifests hearing impairment and abnormal behavior
Mutation Rate Switch inside Eurasian Mitochondrial Haplogroups: Impact of Selection and Consequences for Dating Settlement in Europe
Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes
Mutagenesis in rodents using the L1 retrotransposon
Mutational analysis of highly conserved aspartate residues essential to the catalytic core of the piggyBac transposase
Mutation of Asn293 to Asp in transmembrane helix VI abolishes agonist-induced but not constitutive activity of the beta(2)-adrenergic receptor
Mutagenesis and Repair Induced by the DNA Advanced Glycation End Product N-2-1-(Carboxyethyl)-2 '-deoxyguanosine in Human Cells
Mutagenic Potential of DNA Glycation: Miscoding by (R)- and (S)-N-2-(1-Carboxyethyl)-2 '-deoxyguanosine
Mutations in the insulin-like factor 3 receptor are associated with osteoporosis
Mutation of SYNE-1, encoding an essential component of the nuclear lamina, is responsible for autosomal recessive arthrogryposis
Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p
Mutations in NSUN2 Cause Autosomal-Recessive Intellectual Disability
Mutation of plasma membrane Ca2+ ATPase isoform 3 in a family with X-linked congenital cerebellar ataxia impairs Ca2+ homeostasis
Mutations and polymorphic BRCA variants transmission in breast cancer familial members
Mutant K-Ras Activation of the Proapoptotic MST2 Pathway Is Antagonized by Wild-Type K-Ras
Mutations in the phenflalanine hydroxylase gene identified in 95 patients with phenylketonuria using novel systems of mutation scanning and specific genotyping based upon thermal melt profiles
Mutation analysis of PAH gene and characterization of a recurrent deletion mutation in Korean patients with phenylketonuria
Mutagenesis of the palmitoylation site in vaccinia virus envelope glycoprotein B5
Mutagenicity of the fullerene C-60-generated singlet oxygen dependent formation of lipid peroxides
Mutational Analysis of the Yeast TRAPP Subunit Trs20p Identifies Roles in Endocytic Recycling and Sporulation
Mutation of inhibitory helix-loop-helix protein Id3 causes gamma delta T-cell lymphoma in mice
Mutation analysis of BRIP1 in male breast cancer cases: a population-based study in Central Italy
Mutational events in LMP1 gene of Epstein-Barr virus in salivary gland lymphoepithelial carcinomas
Mutant huntingtin and mitochondrial dysfunction
Mutant huntingtin%26apos;s interaction with mitochondrial protein Drp1 impairs mitochondrial biogenesis and causes defective axonal transport and synaptic degeneration in Huntington%26apos;s disease
Mutant huntingtin binds the mitochondrial fission GTPase dynamin-related protein-1 and increases its enzymatic activity
Mutagenesis of the herpesvirus saimiri terminal repeat region reveals important elements for virus production
Mutations in N-cadherin and a Stardust homolog, Nagie oko, affect cell-cycle exit in zebrafish retina
Mutagenesis reveals a role for ABP/GRIP binding to GluR2 in synaptic surface accumulation of the AMPA receptor
Mutation of HAIRY-AND-ENHANCER-OF-SPLIT-7 in humans causes spondylocostal dysostosis
Mutations Affecting the BHLHA9 DNA-Binding Domain Cause MSSD, Mesoaxial Synostotic Syndactyly with Phalangeal Reduction, Malik-Percin Type
Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity
Mutational, Functional, and Expression Studies of the TCF4 Gene in Pitt-Hopkins Syndrome
Mutations in TCF4, encoding a class I basic helix-loop-helix transcription factor, are responsible for Pitt-Hopkins syndrome, a severe epileptic encephalopathy associated with autonomic dysfunction
Mutagenesis strategies in zebrafish for identifying genes involved in development and disease
Mutations in protein kinase subdomain X differentially affect MEKK2 and MEKK1 activity
Mutant presenilin 2 increases acetylcholinesterase activity in neuronal cells
Mutations in the midway gene disrupt a Drosophila acyl coenzyme A: Diacylglycerol acyltransferase
Mutagenesis of the putative sterol-sensing domain of yeast Niemann Pick C-related protein reveals a primordial role in subcellular sphingolipid distribution
Mutant Presenilin 1 Increases the Expression and Activity of BACE1
Mutant Amyloid Precursor Protein Differentially Alters Adipose Biology under Obesogenic and Non-Obesogenic Conditions
Mutations in Potassium Channel KCND3 Cause Spinocerebellar Ataxia Type 19
Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia
Mutations in PDYN are not responsible for multiple system atrophy
Mutations in String/CDC25 inhibit cell cycle re-entry and neurodegeneration in a Drosophila model of Ataxia telangiectasia
Mutations in the Membrane-Proximal Region of the Influenza A Virus M2 Protein Cytoplasmic Tail Have Modest Effects on Virus Replication
Mutations of Basal Core Promoter and Precore Regions in Hepatitis B Virus Genotypes B and C
Mutagenicity and Potential Carcinogenicity of Thiopurine Treatment in Patients with Inflammatory Bowel Disease
Mutational definition of functional domains within the Rev homolog encoded by human endogenous retrovirus K
Mutation of alpha(1G) T-type calcium channels in mice does not change anesthetic requirements for loss of the righting reflex and minimum alveolar concentration but delays the onset of anesthetic induction
Mutations in pre-core and basal-core promoter regions of hepatitis B virus in chronic HBV patients from Golestan, Iran
Mutation of the P13 ' kinase gene in a human colon carcinoma cell line, HCC2998
Mutations in Cdh23 cause nonsyndromic hearing loss in waltzer mice
Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D
Mutant Prpf31 causes pre-mRNA splicing defects and rod photoreceptor cell degeneration in a zebrafish model for Retinitis pigmentosa
Mutational Ataxia Resulting From Abnormal Vestibular Acquisition and Processing Is Partially Compensated For
Mutations of ASXL1 gene in myeloproliferative neoplasms
Mutational and clinico-pathological analysis of papillary thyroid carcinoma in Serbia
Mutational Screening of RET, HRAS, KRAS, NRAS, BRAF, AKT1, and CTNNB1 in Medullary Thyroid Carcinoma
Mutant p53 Aggregates into Prion-like Amyloid Oligomers and Fibrils IMPLICATIONS FOR CANCER
Mutant p53: one name, many proteins
Mutations in a plasma membrane Ca2+-ATPase gene cause deafness in deafwaddler mice
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D
Mutations in the calcium-binding motifs of CDH23 and the 35delG mutation in GJB2 cause hearing loss in one family
Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution
Mutations in the P3 Protein of Soybean mosaic virus G2 Isolates Determine Virulence on Rsv4-Genotype Soybean
Mutation of tagO reveals an essential role for wall teichoic acids in Staphylococcus epidermidis biofilm development
Mutational Spectrum of SLC4A11 in Autosomal Recessive CHED in Saudi Arabia
Mutations in LOXHD1, a Recessive-Deafness Locus, Cause Dominant Late-Onset Fuchs Corneal Dystrophy
Mutation analysis of the SLC4A11 gene in Indian families with congenital hereditary endothelial dystrophy 2 and a review of the literature
Mutated TATA-box/TATA binding protein complementation system for regulated transgene expression in tobacco
Mutagenesis studies of the beta I domain metal ion binding sites on integrin alpha V beta 3 ligand binding affinity
Mutations and polymorphisms of estrogens receptors genes and diseases susceptibility
Mutation of neutralizing/antibody-dependent enhancing epitope on spike protein and 7b gene of feline infectious peritonitis virus: Influences of viral replication in monocytes/macrophages and virulence in cats
Mutational analysis of active site residues in the Staphylococcus aureus transpeptidase SrtA
Mutagenic and clastogenic characterization of poststerilized poly(3-hydroxybutyrate-co-4-hydroxybutyrate) copolymer biosynthesized by Delftia acidovorans
Mutational Analysis of cis-Acting RNA Signals in Segment 7 of Influenza A Virus
Mutational effects on stability are largely conserved during protein evolution
Mutational Analysis of Candida albicans SNF7 Reveals Genetically Separable Rim101 and ESCRT Functions and Demonstrates Divergence in bro1-Domain Protein Interactions
Mutations in NR2E3 Can Cause Dominant or Recessive Retinal Degenerations in the Same Family
Mutational analysis of the gephyrin-related molybdenum cofactor biosyndietic gene cnxE from the lower eukaryote Aspergillus nidulans
Mutation of Y-179 on phospholipase D2 (PLD2) upregulates DNA synthesis in a PI3K- and Akt-dependent manner
Mutant p53 interactome identifies nardilysin as a p53R273H-specific binding partner that promotes invasion
Mutagenic properties of PM2.5 urban pollution in the Northern Italy: The nitro-compounds contribution
Mutations in KCNJ5 Gene Cause Hyperaldosteronism
Mutations of p53 gene in gastric carcinoma in Taiwan
Mutagen influence with different mechanisms of action on DNA global methylation in human whole-blood lymphocytes in vitro
Mutations of acetylcholinesterase which confer insecticide resistance in insect populations
Mutation Analysis of BRCA1, BRCA2, PALB2 and BRD7 in a Hospital-Based Series of German Patients with Triple-Negative Breast Cancer
Mutations in the long QT gene, KCNQ1, are an uncommon cause of atrial fibrillation
Mutation in the KCNQ1 gene leading to the short QT-interval syndrome
Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humans
Mutational analysis of fibrillarin and its mobility in living human cells
Mutagenesis strategies for identifying novel loci associated with disease phenotypes
Mutagenesis by retroviral insertion in chemical mutagen-gene rated quasi-haploid mammalian cells
Mutation rate in stem cells: an underestimated barrier on the way to therapy
Mutational Pathway Determines Whether Drug Gradients Accelerate Evolution of Drug-Resistant Cells
Mutations in tap uncouple RNA export activity from translocation through the nuclear pore complex
Mutation of siRNA results in thermodynamically unstable duplex which influences knockdown of dmrt1 by RNA interference
Mutational analyses of the putative calcium binding site and hinge of the turnip crinkle virus coat protein
Mutations in exons 2 and 3 of the FOLR1 gene in demented and non-demented elderly subjects
Mutated genes, pathways and processes in tumours
Mutations in acetylcholinesterase associated with insecticide resistance in the cotton aphid, Aphis gossypii Glover (vol 34, pg 397, 2004)
Mutator pathways unleashed by epigenetic silencing in human cancer
Mutations in the Arabidopsis VAR2 locus cause leaf variegation due to the loss of a chloroplast FtsH protease
Mutation of the zebrafish glass onion locus causes early cell-nonautonomous loss of neuroepithelial integrity followed by severe neuronal patterning defects in the retina
Mutations of NPM1 gene in de novo acute myeloid leukaemia: determination of incidence, distribution pattern and identification of two novel mutations in Indian population
Mutagenesis of the active-site cysteine in the ubiquitin-specific protease contained in large tegument protein pUL36 of Pseudorabies virus impairs viral replication in vitro and neuroinvasion in vivo
Mutations Conferring a Noncytotoxic Phenotype on Chikungunya Virus Replicons Compromise Enzymatic Properties of Nonstructural Protein 2
Mutations in the Saccharomyces cerevisiae Kinase Cbk1p Lead to a Fertility Defect That Can Be Suppressed by the Absence of Brr1p or Mpt5p (Puf5p), Proteins Involved in RNA Metabolism
Mutation in Caenorhabditis elegans Kruppel-like factor, KLF-3 results in fat accumulation and alters fatty acid composition
Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss
Mutations causing syndromic autism define an axis of synaptic pathophysiology
Mutations in progranulin (GRN) within the spectrum of clinical and pathological phenotypes of frontotemporal dementia
Mutations in progranulin gene: Clinical, pathological, and ribonucleic acid expression findings
Mutations in the gene phospholipase C, delta-1 (PLCD1) underlying hereditary leukonychia
Mutations in the Stalk Region of the Measles Virus Hemagglutinin Inhibit Syncytium Formation but Not Virus Entry
Mutation adjacent to the active site tyrosine can enhance DNA cleavage and cell killing by the TOPRIM Gly to Ser mutant of bacterial topoisomerase I
Mutations in EDM2 selectively affect silencing states of transposons and induce plant developmental plasticity
Mutagen sensitivity and genetic variants in nucleotide excision repair pathway: Genotype-phenotype correlation
Mutagenesis of Varicella-Zoster Virus Glycoprotein B: Putative Fusion Loop Residues Are Essential for Viral Replication, and the Furin Cleavage Motif Contributes to Pathogenesis in Skin Tissue In Vivo
Mutant p53(R273H) attenuates the expression of phase 2 detoxifying enzymes and promotes the survival of cells with high levels of reactive oxygen species
Mutations in the SLC2A9 Gene Cause Hyperuricosuria and Hyperuricemia in the Dog
Mutational analysis supports a core role for Drosophila alpha-Catenin in adherens junction function
Mutation within TARDBP Leads to Frontotemporal Dementia without Motor Neuron Disease
Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6
Mutant superoxide dismutase 1 overexpression in NSC-34 cells: Effect of trehalose on aggregation, TDP-43 localization and levels of co-expressed glycoproteins
Mutations in the GGCX and ABCC6 Genes in a Family with Pseudoxanthoma Elasticum-Like Phenotypes
Mutation of a raft-targeting signal in the transmembrane region retards transport of influenza virus hemagglutinin through the Golgi
Mutation analysis of the Uromodulin gene in 96 individuals with urinary tract anomalies (CAKUT)
Mutations in AtPS1(Arabidopsis thaliana Parallel Spindle 1) Lead to the Production of Diploid Pollen Grains
Mutations in the calcium-related gene IL1RAPL1 are associated with autism
Mutations in the LRRK2 Roc-COR tandem domain link Parkinson's disease to Wnt signalling pathways
Mutations of a Single Gene: Cause for Ataxia, Amyotrophic Lateral Sclerosis or Tremor
Mutant alpha-Synuclein Overexpression Mediates Early Proinflammatory Activity
Mutation in keratin 18 induces mitochondrial fragmentation in liver-derived epithelial cells
Mutations in pimE restore lipoarabinomannan synthesis and growth in a Mycobacterium smegmatis lpqW mutant
Mutation Update for the PORCN Gene
Mutations in Specific Codons of the KRAS Oncogene are Associated with Variable Resistance to Neoadjuvant Chemoradiation Therapy in Patients with Rectal Adenocarcinoma
Mutation of IGFBP7 Causes Upregulation of BRAF/MEK/ERK Pathway and Familial Retinal Arterial Macroaneurysms
Mutation screening of VHL gene in a family with malignant bilateral pheochromocytoma: from isolated familial pheochromocytoma to von Hippel-Lindau disease
Mutation Analysis of BRAF, MEK1 and MEK2 in 15 Ovarian Cancer Cell Lines: Implications for Therapy
Mutations in the Phosphatidylinositol-3-Kinase Pathway Predict for Antitumor Activity of the Inhibitor PX-866 whereas Oncogenic Ras Is a Dominant Predictor for Resistance
Mutational Profile of Advanced Primary and Metastatic Radioactive Iodine-Refractory Thyroid Cancers Reveals Distinct Pathogenetic Roles for BRAF, PIK3CA, and AKT1
Mutational profiling reveals PIK3CA mutations in gallbladder carcinoma
Mutation and copy number detection in human cancers using a custom genotyping assay
Mutational activation of FGFR3: no involvement in the development of renal cell carcinoma
Mutation profiling identifies numerous rare drug targets and distinct mutation patterns in different clinical subtypes of breast cancers
Mutation of Gtf2ird1 from the Williams-Beuren syndrome critical region results in facial dysplasia, motor dysfunction, and altered vocalisations
Mutational pathways and genetic barriers to CXCR4-mediated entry by human immunodeficiency virus type 1
Mutant huntingtin causes defective actin remodeling during stress: defining a new role for transglutaminase 2 in neurodegenerative disease
Mutational analysis of TARDBP in neurodegenerative diseases
Mutation screening of C1 inhibitor gene in 108 unrelated families with hereditary angioedema: Functional and structural correlates
Mutational spectrum and phenotypes in Danish families with hereditary angioedema because of C1 inhibitor deficiency
Mutations in the Survival Motor Neuron (SMN) Protein Alter the Dynamic Nature of Nuclear Bodies
Mutation of thyroid hormone receptor-beta in mice predisposes to the development of mammary tumors
Mutant Prolactin Receptor and Familial Hyperprolactinemia
Mutant Huntingtin N-terminal Fragments of Specific Size Mediate Aggregation and Toxicity in Neuronal Cells
Mutant Macaque Factor IX T262A: A Tool for Hemophilia B Gene Therapy Studies in Macaques
Mutations in the nef and vif genes associated with progression to AIDS in elite controller and slow-progressor Patients
Mutant PIK3CA licenses TRAIL and CD95L to induce non-apoptotic caspase-8-mediated ROCK activation
Mutant KRAS-Induced Expression of ICAM-1 in Pancreatic Acinar Cells Causes Attraction of Macrophages to Expedite the Formation of Precancerous Lesions
Mutations in Myeloid Neoplasms
Mutational and functional analysis of Large in a novel CHO glycosylation mutant
Mutation of Prkar1a causes osteoblast neoplasia driven by dysregulation of protein kinase A
Mutations and polymorphisms in FSH receptor: functional implications in human reproduction
Mutations in the TTDN1 Gene Are Associated with a Distinct Trichothiodystrophy Phenotype
Mutations in TFIIH causing trichothiodystrophy are responsible for defects in ribosomal RNA production and processing
Mutational Spectrum of Multiple Endocrine Neoplasia Type 2 and Sporadic Medullary Thyroid Carcinoma in Taiwan
Mutational and transcriptional analyses of an avian pathogenic Escherichia coli CoIV plasmid
Mutations in NR5A1 Associated with Ovarian Insufficiency
Mutation Analysis of NR5A1 Encoding Steroidogenic Factor 1 in 77 Patients with 46, XY Disorders of Sex Development (DSD) Including Hypospadias
Mutation in the DNA-binding domain of the EWS-Oct-4 oncogene results in dominant negative activity that interferes with EWS-Oct-4-mediated transactivation
Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation
Mutations in 2 distinct genetic pathways result in cerebral cavernous malformations in mice
Mutation of Actin Tyr-53 Alters the Conformations of the DNase I-binding Loop and the Nucleotide-binding Cleft
Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease
Mutations in a novel serine protease PRSS56 in families with nanophthalmos
Mutation of zebrafish dihydrolipoamide branched-chain transacylase E2 results in motor dysfunction and models maple syrup urine disease
Mutation analysis of three genes in patients with maturation arrest of spermatogenesis and couples with recurrent miscarriages
Mutation analysis of cases of sudden unexplained death, 15 years after death: Prompt genetic evaluation after resuscitation can save future lives
Mutational Status of KIT and PDGFRA and Expression of PDGFRA Are Not Associated With Prognosis After Curative Resection of Primary Gastrointestinal Stromal Tumors (GISTs)
Mutational profile of KIT and PDGFRA genes in gastrointestinal stromal tumors in Peruvian samples
Mutational analysis of the purine riboswitch aptamer domain
Mutational spectrum of F8 gene and prothrombotic gene variants in haemophilia A patients from Southern Italy
Mutation Reporter Tool: An online tool to interrogate loci of interest, with its utility demonstrated using hepatitis B virus
Mutant mice derived by ICSI of evaporatively dried spermatozoa exhibit expected phenotype
Mutational analysis of Deinococcus radiodurans bacteriophytochrome reveals key amino acids necessary for the photochromicity and proton exchange cycle of phytochromes
Mutation of the Rb1 Pathway Leads to Overexpression of mTor, Constitutive Phosphorylation of Akt on Serine 473, Resistance to Anoikis, and a Block in c-Raf Activation
Mutation analysis of gene PAX6 in human gliomas
Mutant PIK3CA promotes cell growth and invasion of human cancer cells
Mutation in the Fe-S scaffold protein Isu bypasses frataxin deletion
Mutations in Calmodulin Cause Ventricular Tachycardia and Sudden Cardiac Death
Mutation of the Calmodulin Binding Motif IQ of the L-type Ca(v)1.2 Ca2+ Channel to EQ Induces Dilated Cardiomyopathy and Death
Mutation of SENP1/SuPr-2 reveals an essential role for desumoylation in mouse development
Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus
Mutations in the central domain of potato virus X TGBp2 eliminate granular vesicles and virus cell-to-cell trafficking
Mutations in NTRK3 Suggest a Novel Signaling Pathway in Human Congenital Heart Disease
Mutations of the Drosophila zinc finger-encoding gene vielfaltig impair mitotic cell divisions and cause improper chromosome segregation
Mutagenesis via IS transposition in Deinococcus radiodurans
Mutations of TGF beta signaling molecules in human disease
Mutant LGI1 inhibits seizure-induced trafficking of Kv4.2 potassium channels
Mutations Derived from the Thermophilic Polyhydroxyalkanoate Synthase PhaC Enhance the Thermo stability and Activity of PhaC from Cupriavidus necator H16
Mutant analysis, protein-protein interactions and subcellular localization of the Arabidopsis B-sister (ABS) protein
Mutation of the Lyn tyrosine kinase delays the progression of Friend virus induced erythroleukemia without affecting susceptibility
Mutations of phosphatase and tensin homolog deleted from chromosome 10 in canine hemangiosarcoma
Mutations in the catalytic subunit of class IA PI3K confer leukemogenic potential to hematopoietic cells
Mutation in the Na+ channel subunit SCN1B produces paradoxical changes in peripheral nerve excitability
Mutant N-RAS induces erythroid lineage dysplasia in human CD34(+) cells
Mutation of three cysteine residues in Tomato yellow leaf curl virus-China C2 protein causes dysfunction in pathogenesis and posttranscriptional gene-silencing suppression
Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F
Mutagenesis of in vitro cultures of Miscanthus x giganteus cultivar Freedom and detecting polymorphisms of regenerated plants using ISSR markers
Mutant huntingtin expression induces mitochondrial calcium handling defects in clonal striatal cells - Functional consequences
Mutations in the glucokinase regulatory protein gene in 2p23 in obese French caucasians
Mutations in Potato virus Y genome-linked protein determine virulence toward recessive resistances in Capsicum annuum and Lycopersicon hirsutum
Mutation and expression of the metastasis suppressor gene KAI1 in esophageal squamous cell carcinoma
Mutagenesis of hepatitis E virus helicase motifs: Effects on enzyme activity
Mutations of nonconserved residues within the calcium channel alpha(1)-interaction domain inhibit beta-subunit potentiation
Mutations of the peripheral antenna complex LH2-correlations of energy transfer time with other functional properties
Mutant Analysis in Arabidopsis Provides Insight into the Molecular Mode of Action of the Auxinic Herbicide Dicamba
Mutations in Sensor 1 and Walker B in the Bovine Papillomavirus E1 Initiator Protein Mimic the Nucleotide-Bound State
Mutation of Asparagine 76 in the Center of Glutamine Transporter SNAT3 Modulates Substrate-induced Conductances and Na+ Binding
Mutation in collagen gene induces cardiomyopathy in transgenic mice
Mutations in the HFE, TFR2, and SLC40A1 genes in patients with hemochromatosis
Mutation frequency vs. mutation patterns: A comparison of the results in spleen and Peyer's patches
Mutant frequencies and spectra depend on growth state and passage number in cells cultured from transgenic lacZ-plasmid reporter mice
Mutations in the human phospholamban gene in patients with heart failure
Mutational and functional analysis of the beta-carotene ketolase involved in the production of canthaxanthin and astaxanthin
Mutagen sensitivity of nasopharyngeal cancer patients
Mutations of extracellular matrix components in vascular disease
Mutation of important amino acid residue of Asp104Lys in human beta(1)-adrenergic receptor triggers functional and constitutive inactivation
Mutational analysis of the gum gene cluster required for xanthan biosynthesis in Xanthomonas oryzae pv oryzae
Mutations in VPS26A are not a frequent cause of Parkinson%26apos;s disease
Mutation in the RNA binding protein TIS11D/ZFP36L2 is associated with the pathogenesis of acute leukemia
Mutant p53 promotes epithelial-mesenchymal plasticity and enhances metastasis in mammary carcinomas of WAP-T mice
Mutations in vacuolar H+-ATPase subunits lead to biliary developmental defects in zebrafish
Mutation of junctophilin type 2 associated with hypertrophic cardiomyopathy
Mutational screening of phospholamban gene in hypertrophic and idiopathic dilated cardiomyopathy and functional study of the PLN-42 C > G mutation
Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction
Mutagenesis of Ly49B Reveals Key Structural Elements Required for Promiscuous Binding to MHC Class I Molecules and New Insights into the Molecular Evolution of Ly49s
Mutation of a TADR Protein Leads to Rhodopsin and G(q)-Dependent Retinal Degeneration in Drosophila
Mutational Analysis of the Pseudomonas aeruginosa Myovirus phi KZ Morphogenetic Protease gp175
Mutation screen of the GAD2 gene and association study of alcoholism in three populations
Mutant acyl-coenzyme A : cholesterol acyltransferase 1 devoid of cysteine residues remains catalytically active
Mutations and microenvironment collude in FL
Mutational unmasking of a tRNA-dependent pathway for preventing genetic code ambiguity
Mutated NPM1 in patients with acute myeloid leukemia in remission and relapse
Mutagen-Specific Mutation Signature Determines Global microRNA Binding
Mutation analysis of the putative tumor suppressor gene PTEN/MMAC1 in advanced gastric carcinomas
Mutations in COX7B Cause Microphthalmia with Linear Skin Lesions, an Unconventional Mitochondrial Disease
Mutation screening of the RNF8, UBC13 and MMS2 genes in Northern Finnish breast cancer families
Mutants at the Slender1 locus of barley cv Himalaya. molecular and physiological characterization
Mutational inactivation of aminoacylase-1 in a small cell hung cancer cell line
Mutations of the lutropin/choriogonadotropin receptor that do not activate the phosphoinositide cascade allow hCG to induce aromatase expression in immature rat granulosa cells
Mutation of an upstream cleavage site in the BMP4 prodomain leads to tissue-specific loss of activity
Mutagenesis and homologous recombination in Drosophila cell lines using CRISPR/Cas9
Mutagenic and genotoxic assessment of atrazine-based herbicide to freshwater fish Channa punctatus (Bloch) using micronucleus test and single cell gel electrophoresis
Mutagenic and genotoxic effects of carbosulfan in freshwater fish Channa punctatus (Bloch) using micronucleus assay and alkaline single-cell gel electrophoresis
Mutagenesis data in the automated prediction of transmembrane helix dimers
Mutation in the lactose permease of Escherichia coli that decreases conformational flexibility and increases protein stability
Mutation spectrum and predicted function of laforin in Lafora's progressive myoclonus epilepsy
Mutations in connexin genes and disease
Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataract
Mutagenic approaches to modifying gap junction phenotype
Mutations in the GIGYF2 (TNRC15) gene at the PARK11 locus in familial Parkinson disease
Mutations in different components of FGF signaling in LADD syndrome (vol 38, pg 424, 2006)
Mutational events during the primary propagation and consecutive passages of hepatitis E virus strain JE03-1760F in cell culture
Mutations within potential glycosylation sites in the capsid protein of hepatitis E virus prevent the formation of infectious virus particles
Mutations in MexB that affect the efflux of antibiotics with cytoplasmic targets
Mutant p53 proteins bind DNA in a DNA structure-selective mode
Mutations in the NF-kappa B signaling pathway: implications for human disease
Mutations at the same residue (R50) of Kir6.2 (KCNJ11) that cause neonatal diabetes produce different functional effects
Mutations within the tyrosine kinase domain of EGFR gene specifically occur in lung adenocarcinoma patients with a low exposure of tobacco smoking
Mutations of the epidermal growth factor receptor gene in gastrointestinal tract tumor cell lines
Mutated PI 3-kinases - Cancer targets on a silver platter
Mutation analysis of NF-kappa B signal pathway-related genes in ocular MALT lymphoma
Mutational analysis of a Dcp2-binding element reveals general enhancement of decapping by 5 '-end stem-loop structures
Mutations in the effector binding loops in the C2A and C2B domains of synaptotagmin I disrupt exocytosis in a nonadditive manner
Mutational analysis of patients with FGF23-related hypophosphatemic rickets
Mutational analysis of PHEX, FGF23, DMP1, SLC34A3 and CLCN5 in patients with hypophosphatemic rickets
Mutational analysis of PHEX, FGF23 and DMP1 in a cohort of patients with hypophosphatemic rickets
Mutations in the gene encoding SLURP-1 in Mel de Meleda
Mutability and mutational spectrum of chromosome transmission fidelity genes
Mutations within the membrane domain of HMG-CoA reductase confer resistance to sterol-accelerated degradation
Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus
Mutagenesis analysis of the nsp4 main proteinase reveals determinants of arterivirus replicase polyprotein autoprocessing
Mutations in Turnip mosaic virus genomes that have adapted to Raphanus sativus
Mutations in Turnip mosaic virus P3 and cylindrical inclusion proteins are separately required to overcome two Brassica napus resistance genes
Mutant Activin-Like Kinase 2 in Fibrodysplasia Ossificans Progressiva are Activated via T203 by BMP Type II Receptors
Mutant p53 induces the GEF-H1 oncogene, a guanine nucleotide exchange factor-H1 for RhoA, resulting in accelerated cell proliferation in tumor cells
Mutation of the Arabidopsis Calmodulin-Like Protein CML37 Deregulates the Jasmonate Pathway and Enhances Susceptibility to Herbivory
Mutations in the chromatin-associated protein ATRX
Mutagenic and carcinogenic hazards of settled house dust I: Polycyclic aromatic hydrocarbon content and excess lifetime cancer risk from preschool exposure
Mutant analyses define multiple roles for phytochrome C in Arabidopsis photomorphogenesis
Mutations in the Arabidopsis gene immutans cause a variegated phenotype by inactivating a chloroplast terminal oxidase associated with phytoene desaturation
Mutagenicity of cadmium in mammalian cells: implication of oxidative DNA damage
Mutagenesis study on the zebra fish SOX9 high-mobility group: Comparison of sequence and non-sequence specific HMG domains
Mutations in G protein-coupled receptors that impact receptor trafficking and reproductive function
Mutant BRAF Melanomas-Dependence and Resistance
Mutations in the activation loop tyrosine of the oncoprotein v-Fps
Mutagenesis studies of human red opsin: Trp-281 is essential for proper folding and protein-retinal interactions
Mutational analysis of the Rhizobium etli recA operator
Mutations and Response to Epidermal Growth Factor Receptor Inhibitors
Mutations of the epidermal growth factor receptor gene and related genes as determinants of epidermal growth factor receptor tyrosine kinase inhibitors sensitivity in lung cancer
Mutations in genes encoding the mitochondrial outer membrane proteins Tom70 and Mdm10 of Podospora anserina modify the spectrum of mitochondrial DNA rearrangements associated with cellular death
Mutations in a sequence near the N-terminus of the small subunit alter the CO2/O-2 specificity factor for ribulose bisphosphate carboxylase/oxygenase
Mutant BCR-ABL clones in chronic myeloid leukemia
Mutant Mouse Models: Phenotypic Relationships to Domains of Psychopathology and Pathobiology in Schizophrenia
Mutant models for genes associated with schizophrenia
Mutational analysis of Yap1 protein, an AP-1-like transcriptional activator of Saccharomyces cerevisiae
Mutational analysis of the angiotensin II type 2 receptor: contribution of conserved extracellular amino acids
Mutations in KCND3 Cause Spinocerebellar Ataxia Type 22
Mutation identification DNA analysis system (MIDAS) for detection of known mutations
Mutation detection and single-molecule counting using isothermal rolling-circle amplification
Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy
Mutation analysis in 46 British and Irish patients with Gaucher's disease
Mutagenesis of recombinant human fibroblast stromelysin C-terminus reveals the autodegradation pathway
Mutational analysis of the ligand binding site of the inositol 1,4,5-trisphosphate receptor
Mutation of the plastidial alpha-glucan phosphorylase gene in rice affects the synthesis and structure of starch in the endosperm
Mutations in the small subunit of ribulose-1,5-bisphosphate carboxylase/oxygenase increase the formation of the misfire product xylulose-1,5-bisphosphate
Mutant vasopressin precursors that cause autosomal dominant neurohypophyseal diabetes insipidus retain dimerization and impair the secretion of wild-type proteins
Mutation and association analysis of GEN1 in breast cancer susceptibility
Mutagenesis of conserved charged amino acids in SLH domains of Thermoanaerobacterium thermosulfurigenes EM1 affects attachment to cell wall sacculi
Mutation screening using fluorescence multiplex denaturing gradient gel electrophoresis (FMD): detecting mutations in the BRCA1 gene
Mutation of El glycoprotein of classical swine fever virus affects viral virulence in swine
Mutations in gidB Confer Low-Level Streptomycin Resistance in Mycobacterium tuberculosis
Mutations in the E-domain of RAR alpha portion of the PML/RAR alpha chimeric gene may confer clinical resistance to all-trans retinoic acid in acute promyelocytic leukemia
Mutation spectrum in the lacI gene, induced by gamma-radiation in aqueous solution under oxic conditions
Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta
Mutation Discovery in Regions of Segmental Cancer Genome Amplifications with CoNAn-SNV: A Mixture Model for Next Generation Sequencing of Tumors
Mutational Signatures of De-Differentiation in Functional Non-Coding Regions of Melanoma Genomes
Mutational analysis of residues forming hydrogen bonds in the Rieske [2Fe-2S] cluster of the cytochrome bc(1) complex in Paracoccus denitrificans
Mutants of Citrobacter freundii that transport and utilize melibiose
Mutation of cis-proline 207 in mitochondrial creatine kinase to alanine leads to increased acid stability
Mutations in the highly conserved GGQ motif of class 1 polypeptide release factors abolish ability of human eRF1 to trigger peptidyl-tRNA hydrolysis
Mutations in the white gene of Drosophila melanogaster affecting ABC transporters that determine eye colouration
Mutational analysis of the main CytR protein binding site within the regulatory region of the Escherichia coli udp gene
Mutations in the promoter reveal a cause for the reduced expression of the human manganese superoxide dismutase gene in cancer cells
Mutational analysis of aspartate residues in the transmembrane regions and cytoplasmic loops of rat vesicular acetylcholine transporter
Mutations of the p53 gene in myelodysplastic syndrome and overt leukaemia
Mutational analysis of the thermostable arginine repressor from Bacillus stearothermophilus: Dissecting residues involved in DNA binding properties
Mutational analysis of a higher plant antenna protein provides identification of chromophores bound into multiple sites
Mutations in the gene encoding the alpha-subunit of the G(s) protein in molar pregnancy
Mutation in the gene encoding the fibroblast growth factor receptor-3 in Korean children with achondroplasia
Mutations of basic amino acids of NCp7 of human immunodeficiency virus type 1 affect RNA binding in vitro
Mutations in ras oncogenes: Rare events in ultraviolet B radiation-induced mouse skin tumorigenesis
Mutant 5-Hydroxytryptamine(1A) Receptor D116A Is a Receptor Activated Solely by Synthetic Ligands with a Rich Pharmacology
Mutational analysis of VACM-1/cul5 exons in cancer cell lines
Mutation of a Single Residue Renders Human Tetherin Resistant to HIV-1 Vpu-Mediated Depletion
Mutational analysis of JAK1 exon 10 and 13 in common solid cancers
Mutations in the neutral sphingomyelinase gene SMPD3 implicate the ceramide pathway in human leukemias
Mutational and functional analysis of HPV-16URR derived from Korean cervical neoplasia
Mutational analysis of the cbb operon (CO2 assimilation) promoter of Ralstonia eutropha
Mutation Screening of the 3q29 Microdeletion Syndrome Candidate Genes DLG1 and PAK2 in Schizophrenia
Mutant p53 Amplifies Epidermal Growth Factor Receptor Family Signaling to Promote Mammary Tumorigenesis
Mutations of EGFR or KRAS and expression of chemotherapy-related genes based on small biopsy samples in stage IIIB and IV inoperable non-small cell lung cancer
Mutations at the BLK locus linked to maturity onset diabetes of the young and beta-cell dysfunction
Mutational analysis of the yeast multidrug resistance ABC transporter Pdr5p with altered drug specificity
Mutagenic specificity of 2-acetylaminonaphthalene-derived DNA adduct in mammalian cells
Mutation and crystallization of the first KH domain of human polycytosine-binding protein 1 (PCBP1) in complex with DNA
Mutation Scanning Using MUT-MAP, a High-Throughput, Microfluidic Chip-Based, Multi-Analyte Panel
Mutagenesis and carcinogenesis induced by dibenzo[a,l]pyrene in the mouse oral cavity: a potential new model for oral cancer
Mutations in the low-density lipoprotein receptor gene in Swedish familial hypercholesterolaemia patients: clinical expression and treatment response
Mutant isolation of the Escherichia coli quinoprotein glucose dehydrogenase and analysis of crucial residues Asp-730 and His-775 for its function
Mutational potentiality of stannous chloride: an important reducing agent in the Tc-99m-radiopharmaceuticals
Mutational inactivation of a gene homologous to Escherichia coli ptsP affects poly-beta-hydroxybutyrate accumulation and nitrogen fiuation in Azotobacter vinelandii
Mutational Analysis and Clinical Correlation of Metastatic Colorectal Cancer
Mutation of the homologue of GDP-mannose pyrophosphorylase alters cell wall structure, protein glycosylation and secretion in Hansenula polymorpha
Mutational analysis of two putative catalytic motifs of the type IV restriction endonuclease Eco57I
Mutant barley (1 -> 3,1 -> 4)-beta-glucan endohydrolases with enhanced thermostability
Mutational definition of RNA-binding and protein-protein interaction domains of heterogeneous nuclear RNP C1
Mutation analysis of the feedback inhibition site of aspartokinase III of Escherichia coli K-12 and its use in L-threonine production
Mutation analysis of the MCM gene in Israeli patients with mut(0) disease
Mutation analysis of the SLX4/FANCP gene in hereditary breast cancer
Mutations for the people
Mutation patterns in cancer genomes
Mutational Analysis of TTK Gene in Gastric and Colorectal Cancers with Microsatellite Instability
Mutational spectra of human cancer
Mutation of Phe413 to Tyr in catalase KatE from Escherichia coli leads to side chain damage and main chain cleavage
Mutation analysis of the MDM4 gene in German breast cancer patients
Mutations in TBX1 genocopy the 22q11.2 deletion and duplication syndromes: a new susceptibility factor for mental retardation
Mutations in the DDR2 Kinase Gene identify a Novel therapeutic target in squamous cell lung cancer
Mutation in MPDZ causes severe congenital hydrocephalus
Mutagenesis of catalytically important residues of cupin type phosphoglucose isomerase from Archaeoglobus fulgidus
Mutants in Phospholipid Signaling Attenuate the Behavioral Response of Adult Drosophila to Trehalose
Mutational analysis of Bacillus subtilis glutamine phosphoribosylpyrophosphate amidotransferase propeptide processing
Mutations of Arg(198) in sarcoplasmic reticulum Ca2+-ATPase cause inhibition of hydrolysis of the phosphoenzyme intermediate formed from inorganic phosphate
Mutational alteration of human immunodeficiency virus type 1 Vif allows for functional interaction with nonhuman primate APOBEC3G
Mutants dissecting development and behaviour in Drosophila
Mutagenic effects at hprt locus and in minisatellite sequences induced in V79 cells by treatments with UV and methyl-nitro-nitroso guanidine
Mutations of the p53 gene as a prognostic factor in aggressive B-cell lymphoma
Mutational analysis of ectopic factor VIII transcripts from hemophilia A patients: identification of cryptic splice site, exon skipping and novel point mutations
Mutational analysis of the C-terminal region of AREA, the transcription factor mediating nitrogen metabolite repression in Aspergillus nidulans
Mutational analysis of the binding affinity and transport activity for N-acetylglucosamine of the novel ABC transporter Ngc in the chitin-degrader Streptomyces olivaceoviridis
Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis
Mutations in DPAGT1 Cause a Limb-Girdle Congenital Myasthenic Syndrome with Tubular Aggregates
Mutations in Bartonella bacilliformis gyrB confer resistance to coumermycin A(1)
Mutations in fliK and flhB affecting flagellar hook and filament assembly in Salmonella typhimurium
Mutational analysis of the pullulanase-type debranching enzyme of maize indicates multiple functions in starch metabolism
Mutational and structural analysis of stem-loop IIIc of the hepatitis C virus and GB virus B internal ribosome entry sites
Mutagenic properties of the 8-amino-2 '-deoxyguanosine DNA adduct in mammalian cells
Mutation in a gene required for lipopolysaccharide and enterobacterial common antigen biosynthesis affects virulence in the plant pathogen Erwinia carotovora subsp atroseptica
Mutation of the N-terminal proline 9 of BLMA from Streptomyces verticillus abolishes the binding affinity for bleomycin
Mutations of the tyrosinase gene in three Korean patients with type I oculocutaneous albinism
Mutation analysis of VCP in familial and sporadic amyotrophic lateral sclerosis
Mutation in C9orf72 changes the boundaries of ALS and FTD
Mutations affecting the development of the peripheral nervous system in drosophila: A molecular screen for novel proteins
Mutation analysis of the tyrosine phosphatase PTPN2 in Hodgkin's lymphoma and T-cell non-Hodgkin's lymphoma
Mutations in a conserved motif inhibit single-stranded DNA binding and recombination mediator activities of bacteriophage T4 UvsY protein
Mutations in alpha-tubulin promote basal body maturation and flagellar assembly in the absence of delta-tubulin
Mutations in the poliovirus 3CD proteinase S1-specificity pocket affect substrate recognition and RNA binding
Mutational analysis of the role of hydrophobic residues in the 338-348 helix on actin in actomyosin interactions
Mutations in the cytoplasmic domain of the integrin beta(1) chain indicate a role for endocytosis factors in bacterial internalization
Mutagenesis of transmembrane domain 11 of P-glycoprotein by alanine scanning
Mutational analysis of the Streptomyces scabies esterase signal peptide
Mutations of Glu92 in ferredoxin I from spinach leaves produce proteins fully functional in electron transfer but less efficient in supporting NADP(+) photoreduction
Mutations in the RNA polymerase II transcription machinery suppress the hyperrecombination mutant hpr1 Delta of Saccharomyces cerevisiae
Mutation of MeCP2 alters transcriptional regulation of select immediate-early genes
Mutations of the adenomatous polyposis coli and p53 genes in a child with Turcot's syndrome
Mutagenic properties of estrogen quinone-derived DNA adducts in simian kidney cells
Mutations of IDH1 and 2 genes in gliomas that condition the acquisition of a "hypermethylator phenotype" in tumors
Mutations at domain II, loop 3, of Bacillus thuringiensis CryIAa and CryIAb delta-endotoxins suggest loop 3 is involved in initial binding to lepidopteran midguts
Mutations in the MGAT2 gene controlling complex N-glycan synthesis cause carbohydrate-deficient glycoprotein syndrome type II, an autosomal recessive disease with defective brain development
Mutations in apbC (mrp) prevent function of the alternative pyrimidine biosynthetic pathway in Salmonella typhimurium
Mutations induced by gamma-irradiation of M13 bacteriophages containing single-stranded DNA
Mutational analysis and chemical modification of Cys24 of lactococcin B, a bacteriocin produced by Lactococcus lactis
Mutations of Different Molecular Origins Exhibit Contrasting Patterns of Regional Substitution Rate Variation
Mutant p53 may selectively suppress glial specific proteins in pluripotential human neuroectodermal tumor cells
Mutagenesis and characterization of specific residues in fatty acid ethyl ester synthase: A gene for alcohol-induced cardiomyopathy
Mutations in the yeast KEX2 gene cause a Vma(-)-like phenotype: a possible role for the KEX2 endoprotease in vacuolar acidification
Mutagenic Effect of Three Nitrogenous Fertilizers on Drosophila melanogaster
Mutation Rate Distribution Inferred from Coincident SNPs and Coincident Substitutions
Mutations in the BRCA1 gene (185delAG and 5382insC) are not present in any of the 30 breast cancer patients analyzed from eastern Colombia
Mutational Analysis of the Respiratory Nitrate Transporter NarK2 of Mycobacterium tuberculosis
Mutational analysis of the mouse somatostatin receptor type 5 gene promoter
Mutations in the intersubunit bridge regions of 16S rRNA affect decoding and subunit-subunit interactions on the 70S ribosome
Mutation of aromatic amino acid residues located at the amino- and carboxy-termini of Escherichia coli heat-stable enterotoxin Ip reduces the efficiency of the toxin to cross the outer membrane
Mutations in the pqe-1 Gene Enhance Transgene Expression in Caenorhabditis elegans
Mutational analysis of breast cancer: Guiding personalized treatments
Mutational analysis of the transcription factor IIIB-DNA target of Ty3 retroelement integration
Mutation analysis of the carbohydrate sulfotransferase gene in Vietnamese with macular corneal dystrophy
Mutations in MITF and PAX3 Cause %26quot;Splashed White%26quot; and Other White Spotting Phenotypes in Horses
Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing
Mutational profiling of familial male breast cancers reveals similarities with luminal A female breast cancer with rare TP53 mutations
Mutations are involved in emergence of aminoglycoside-induced small colony variants of Staphylococcus aureus
Mutagenesis of the conserved active-site tyrosine changes a retaining sialidase into an inverting sialidase
Mutation rate and evolution of fluoroquinolone resistance in Escherichia coli isolates from patients with urinary tract infections
Mutational analysis and localization of the inositol transporters of Saccharomyces cerevisiae
Mutations in the reduced-folate carrier affect protein localization and stability
Mutations in yhiT enable utilization of exogenous pyrimidine intermediates in Salmonella enterica serovar Typhimurium
Mutagenesis of charged residues in a conserved sequence in the 2-kinase domain of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase
Mutations of the 5 alpha-reductase type 2 gene in eight Mexican patients from six different pedigrees with 5 alpha-reductase-2 deficiency
Mutations in CSTA, Encoding Cystatin A, Underlie Exfoliative Ichthyosis and Reveal a Role for This Protease Inhibitor in Cell-Cell Adhesion
Mutational profiles in triple-negative breast cancer defined by ultradeep multigene sequencing show high rates of PI3K pathway alterations and clinically relevant entity subgroup specific differences
Mutations in ccf, a novel Drosophila gene encoding a chromosomal factor, affect progression through mitosis and interact with Pc-G mutations
Mutagenic specificity of the food mutagen 2-amino-3-methylimidazo[4,5-f]quinoline in Escherichia coli using the yeast URA3 gene as a target
Mutational analysis of UMP kinase from Escherichia coli
Mutational analysis of the Streptomyces lividans recA gene suggests that only mutants with residual activity remain viable
Mutational analyses of the enzymes involved in the metabolism of hydrogen by the hypertherrnophilic archaeon Pyrococcus furiosus
Mutant Enrichment with 3 '-Modified Oligonucleotides A Practical PCR Method for Detecting Trace Mutant DNAs
Mutation Detection by Real-Time PCR: A Simple, Robust and Highly Selective Method
Mutations of the Huntington's Disease Protein Impact on the ATM-Dependent Signaling and Repair Pathways of the Radiation-Induced DNA Double-Strand Breaks: Corrective Effect of Statins and Bisphosphonates
Mutant telomerase RNAs induce DNA damage and apoptosis via the TRF2-ATM pathway in telomerase-overexpressing primary fibroblasts
Mutant alleles of Schizosaccharomyces pombe rad9(+) alter hydroxyurea resistance, radioresistance and checkpoint control
Mutational analysis of two structural genes of the temperate lactococcal bacteriophage TP901-1 involved in tail length determination and baseplate assembly
Mutational analysis of the neuronal cadherin gene CELSR1 and exclusion as a candidate for catatonic schizophrenia in a large family
Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy
Mutation Detection by TaqMan-allele specific amplification: Application to molecular diagnosis of glycogen storage disease type Ia and medium-chain acyl-CoA dehydrogenase deficiency
Mutational bias affects protein evolution in flowering plants
Mutation in and lack of expression of tyrosinase-related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism: A new subtype of albinism classified as ''OCA3''
Mutations in the Ty3 major homology region affect multiple steps in Ty3 retrotransposition
Mutagenic and nonmutagenic bypass of DNA lesions by Drosophila DNA polymerases dpol eta and dpol iota
Mutational analysis of the Drosophila homothorax gene
Mutations associated with hemophilia B in Turkish patients
Mutational analysis of stubble-stubbloid gene structure and function in Drosophila leg and bristle morphogenesis
Mutations in Complement Regulatory Proteins Predispose to Preeclampsia: A Genetic Analysis of the PROMISSE Cohort
Mutation spectrum and phenylalanine hydroxylase RFLP/VNTR background in 44 Romanian phenylketonuric alleles
Mutation of C-terminal tyrosine residues Y497/Y504 of the Src-family member Bsk/Iyk decreases NIH3T3 cell proliferation
Mutations of the DRY motif that preserve beta 2-adrenoceptor coupling
Mutational screening of VSX1, SPARC, SOD1, LOX, and TIMP3 in keratoconus
Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome
Mutations in the tail domain of DYNC1H1 cause dominant spinal muscular atrophy
Mutations in CTC1, Encoding the CTS Telomere Maintenance Complex Component 1, Cause Cerebroretinal Microangiopathy with Calcifications and Cysts
Mutations in the Corneal Endothelial Dystrophy-Associated Gene SLC4A11 Render the Cells More Vulnerable to Oxidative Insults
Mutation analysis of glycine decarboxylase, aminomethyltransferase and glycine cleavage system protein-H genes in 13 unrelated families with glycine encephalopathy
Mutations in POLE and survival of colorectal cancer patients - link to disease stage and treatment
Mutagens manufactured in fungal culture may affect DNA/RNA of producing fungi
Mutations in ligands and receptors of the leptin-melanocortin pathway that lead to obesity
Mutations to the histone H3 N region selectively alter the outcome of ATP-dependent nucleosome-remodelling reactions
Mutation load, functional overlap, and synthetic lethality in the evolution and treatment of cancer
Mutation in the ligand-binding domain of the retinoic acid receptor alpha in HL-60 leukemic cells resistant to retinoic acid and with increased sensitivity to vitamin D-3 analogs
Mutation of the sialyltransferase S-sialylmotif alters the kinetics of the donor and acceptor substrates
Mutations in the sindbis virus capsid gene can partially suppress mutations in the cytoplasmic domain of the virus E2 glycoprotein spike
Mutational analysis of the four alpha-helix bundle iron-loading channel of rat liver ferritin
Mutational analysis of the function of Met137 and Ile197, two amino acids implicated in sequence-specific DNA recognition by the EcoRI endonuclease
Mutation frequency of PRKAR1B and the major familial dementia genes in a Dutch early onset dementia cohort
Mutational specificity of 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea in Escherichia coli comparison of in vivo with in vitro exposure of the supF gene
Mutation in splicing consensus sequences causes lack of TCR membrane expression due to exon excision
Mutational analysis of receptor binding mediated by the Dr family of Escherichia coli adhesins
Mutational analysis of the L1 neuronal cell adhesion molecule identifies membrane-proximal amino acids of the cytoplasmic domain that are required for cytoskeletal anchorage
Mutation of cysteine-115 to alanine in Nicotiana glutinosa ornithine decarboxylase reduces enzyme activity
Mutation of a gene in the fungus Leptosphaeria maculans allows increased frequency of penetration of stomatal apertures of Arabidopsis thaliana
Mutational analysis of the conserved motif of the ArdA antirestriction protein encoded by self-transmissible IncI plasmid ColIb-P9
Mutation analysis of five new patients affected by prolidase deficiency: the lack of enzyme activity causes necrosis-like cell death in cultured fibroblasts
Mutations in human immunodeficiency virus type 1 RNase H primer grip enhance 3-Azido-3'-deoxythymidine resistance
Mutations of the cystic fibrosis gene in patients with bronchiectasis associated with rheumatoid arthritis
Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome
Mutational analysis of parkin and PINK1 in multiple system atrophy
Mutational and functional analysis of the C-terminal region of the C3H mouse mammary tumor virus superantigen
Mutational specificity of the ferrous ion in a supF gene of endonuclease III/VIII deficient Escherichia coli
Mutations in the carboxy-terminal part of IS30 transposase affect the formation and dissolution of (IS30)(2) dimer
Mutational profiling of sporadic versus toxin-associated brain cancer formation: Initial findings using loss of heterozygosity profiling
Mutations in beta-spectrin disrupt axon outgrowth and sarcomere structure
Mutant frequency at the Hprt locus and in minisatellite sequences in Chinese hamster V79 cells irradiated with low-energy protons (31 keV/mu m) and ultraviolet light (254 nm)
Mutational analysis of the Chlamydia trachomatis rRNA P1 promoter defines four regions important for transcription in vitro
Mutation of threonine-53 alters the kinetic properties of rubisco from Rhodospirillum rubrum
Mutational activation of pp60(c-src) leads to a tumorigenic phenotype in a preneoplastic syrian hamster embryo cell line
Mutations that cause threonine sensitivity identify catalytic and regulatory regions of the aspartate kinase of Saccharomyces cerevisiae
Mutagenesis of the N-(deoxyguanosin-8-yl)-2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine DNA adduct in mammalian cells - Sequence context effects
Mutation spectrum induced by singlet oxygen in Escherichia coli deficient in exonuclease III
Mutants that alter the covalent structure of catalase hydroperoxidase II from Escherichia coli
Mutations in PNKP Cause Recessive Ataxia with Oculomotor Apraxia Type 4
Mutations in Intracellular Loops 1 and 3 Lead to Misfolding of Human P-glycoprotein (ABCB1) That Can Be Rescued by Cyclosporine A, Which Reduces Its Association with Chaperone Hsp70
Mutations altering the specificity of the sensor RNA encoded by the Bacillus subtilis pbuE gene
Mutations at different sites in members of the Gpr1/Fun34/YaaH protein family cause hypersensitivity to acetic acid in Saccharomyces cerevisiae as well as in Yarrowia lipolytica
Mutations in the TORNADO2 gene affect cellular decisions in the peripheral zone of the shoot apical meristem of Arabidopsis thaliana
Mutational analyses of a single-stranded telomeric DNA binding domain of fission yeast Pot1: Conflict with X-ray crystallographic structure
Mutational analysis of genes encoding chromatin proteins in the archaeon Methanococcus voltae indicates their involvement in the regulation of gene expression
Mutational analysis of the endothelin type A receptor (ET(A)): Interactions and model of the selective ET(A) antagonist EMS-182874 with the putative ET(A) receptor binding cavity
Mutagenic effects of tumorigenic neutron radiation
Mutations within the first LSGGQ motif of Ste6p cause defects in a-factor transport and mating in Saccharomyces cerevisiae
Mutational analysis identifies functional domains in the influenza A virus PB2 polymerase subunit
Mutations in the gene for human dihydrofolate reductase: An unlikely cause of clinical relapse in pediatric leukemia after therapy with methotrexate
Mutational analysis of Escherichia coli PepA, a multifunctional DNA-binding aminopeptidase
Mutational analysis of regulatory cis-acting elements for the transcriptional activation of the dmsCBA operon in Rhodobacter sphaeroides f. sp denitrificans
Mutational analysis of PHEX gene in X-linked hypophosphatemia
Mutational analysis of the bacteriophage P4 capsid-size-determining gene
Mutations in motB suppressible by changes in stator or rotor components of the bacterial flagellar motor
Mutations responsible for reduced susceptibility to 4-quinolones in clinical isolates of multi-resistant Salmonella typhi in India
Mutant G-protein-coupled receptors as a cause of human diseases
Mutated epitopes of hepatitis B surface antigen fused to the core antigen of the virus induce antibodies that react with the native surface antigen
Mutation of Glu-361 in human endothelial nitric-oxide synthase selectively abolishes L-arginine binding without perturbing the behavior of heme and other redox centers
Mutations in the 1.1 subdomain of Escherichia coli sigma factor sigma(70) and disruption of its overall structure
Mutant T7 RNA polymerase is capable of catalyzing DNA primer extension reaction
Mutant ATP-binding RNA aptamers reveal the structural basis for ligand binding
Mutational analysis of the protein subunits of the signal recognition particle Alu-domain
Mutations at nucleotides G2251 and U2585 of 23 S rRNA perturb the peptidyl transferase center of the ribosome
Mutations at a glycine loop in aminolevulinate synthase affect pyridoxal phosphate cofactor binding and catalysis
Mutational analysis of the A-kinase anchoring protein (AKAP)-binding site on RII - Classification of side chain determinants for anchoring and isoform selective association with AKAPs
Mutation in the cobO gene generates auxotrophy for cobalamin and methionine and impairs the symbiotic properties of Sinorhizobium fredii HH103 with soybean and other legumes
Mutational analysis in chronic myeloid leukemia: when and what to do?
Mutagenic consequences of the incorporation of 6-thioguanine into DNA
Mutational analysis of domain II of flavonol 3-sulfotransferase
Mutagenesis reveals structure-activity parallels between human A(2A) adenosine receptors and biogenic amine G protein-coupled receptors
Mutations of the conserved DRS motif in the second intracellular loop of the gonadotropin-releasing hormone receptor affect expression, activation, and internalization
Mutational analysis of Escherichia coli elongation factor Tu in search of a role for the N-terminal region
Mutational analysis of the input domain of the VirA protein of Agrobacterium tumefaciens
Mutational analysis of PTEN/PIK3CA/AKT pathway in oral squamous cell carcinoma
Mutational analysis of the Caenorhabditis elegans ankyrin gene unc-44 demonstrates that the large spliceoform is critical for neural development
Mutations within the putative active site of heterodimeric deoxyguanosine kinase block the allosteric activation of the deoxyadenosine kinase subunit
Mutation screening of the human lipoprotein lipase gene in Korean individuals with essential hypertension
Mutation in the Xanthomonas campestris xanA gene required for synthesis of xanthan and lipopolysaccharide drastically reduces the efficiency of bacteriophage phi L7 adsorption
Mutations of the p53 gene in canine lymphoma and evidence for germ line p53 mutations in the dog
Mutations in the long control region of human papillomavirus DNA in oral cancer cells, and their functional consequences
Mutational analysis of the 5 ' leader region of simian foamy virus type 1
Mutation detection by pyrosequencing: sequencing of exons 5-8 of the p53 tumor suppressor gene
Mutations in Bone Morphogenetic Protein Receptor Genes in Pulmonary Arterial Hypertension Patients - Possible Involvement of BMPRIB
Mutation and methylation analysis of the transforming growth factor beta receptor II gene in polycythaemia vera
Mutational analysis of amiloride sensitivity of the NhaA Na+/H+ antiporter from Vibrio parahaemolyticus
Mutational analysis of the three cysteines and active-site aspartic acid 103 of ketosteroid isomerase from Pseudomonas putida biotype B
Mutations in two distinct regions of acetolactate synthase regulatory subunit from Streptomyces cinnamonensis result in the lack of sensitivity to end-product inhibition
Mutational analysis of Asp51 of Anabaena azollae glutamine synthetase. D51E mutation confers resistance to the active site inhibitors L-methionine-DL-sulfoximine and phosphinothricin
Mutation of aspartic acid residues in the fructosyltransferase of Streptococcus salivarius ATCC 25975
Mutational analysis in murine models for myeloma-associated Fanconi's syndrome or cast myeloma nephropathy
Mutations in the carboxyl-terminal hydrophobic sequence of human cytomegalovirus glycoprotein B alter transport and protein chaperone binding
Mutational analysis on the RNA helicase domain of the yeast ROK1 gene
Mutational analysis of two highly conserved UGG sequences of 23 S rRNA from Escherichia coli
Mutation of lysines in a plasminogen binding region of streptokinase identifies residues important for generating a functional activator complex
Mutant HSPB8 causes protein aggregates and a reduced mitochondrial membrane potential in dermal fibroblasts from distal hereditary motor neuropathy patients
Mutational evidence of transition state stabilization by Serine 88 in Escherichia coli type I signal peptidase
Mutations in GAL2 or GAL4 alleviate catabolite repression produced by galactose in Saccharomyces cerevisiae
Mutational analysis of the substrate binding/catalytic domains of human M form and P form phenol sulfotransferases
Mutation analysis of cadherin-4 reveals amino acid residues of EC1 important for the structure and function
Mutations in the beta Subunit of RNA Polymerase Alter Intrinsic Cephalosporin Resistance in Enterococci
Mutation and epigenetic molecular clocks in cancer
Mutation analysis of very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency: Identification and characterization of mutant VLCAD cDNAs from four patients
Mutational analysis of the alpha subunit of the human interleukin-3 receptor
Mutations in the PI3K/PTEN/TSC2 pathway contribute to mammalian target of rapamycin activity and increased translation under hypoxic conditions
Mutations at arg486 and glu571 in human topoisomerase II alpha confer resistance to amsacrine: Relevance for antitumor drug resistance in human cells
Mutant residues suppressing rho(0)-lethality in Kluyveromyces lactis occur at contact sites between subunits of F-1-ATPase
Mutational analysis of basic residues in the rat vesicular acetylcholine transporter - Identification of a transmembrane ion pair and evidence that histidine is not involved in proton translocation
Mutations induced by some DNA minor groove binding alkylators in AS52 Chinese hamster cells
Mutations in the 5 ' trailer region of a respiratory syncytial virus minigenome which limit RNA replication to one step
Mutated Atf4 suppresses c-Ha-ras oncogene transcript levels and cellular transformation in NIH3T3 fibroblasts
Mutations in the ATM gene lead to impaired overall and treatment-free survival that is independent of IGVH mutation status in patients with B-CLL
Mutations in POLR3A and POLR3B Encoding RNA Polymerase III Subunits Cause an Autosomal-Recessive Hypomyelinating Leukoencephalopathy
Mutational Analysis Reveals the Origin and Therapy-Driven Evolution of Recurrent Glioma
Mutations within the primer binding site of the human immunodeficiency virus type 1 define sequence requirements essential for reverse transcription
Mutants in position 69 of the Trp repressor of Escherichia coli K12 with altered DNA binding specificity
Mutational analysis of N-linked glycosylation of esterase 6 in Drosophila melanogaster
Mutations of non-canonical base-pairs in the 3' major domain of Escherichia coli 16 S ribosomal RNA affect the initiation and elongation of protein synthesis
Mutated-gamma-actin restores growth to a yeast amino acid transport defective mutant
Mutations in the low-density-lipoprotein receptor gene in German patients with familial hypercholesterolaemia
Mutations truncating the EP300 acetylase in human cancers
Mutations in the f165(1)A and f165(1)E fimbrial genes and regulation of their expression in an Escherichia coli strain causing septicemia in pigs
Mutant forms of the enhancer-binding protein NtrC can activate transcription from solution
Mutation of a lysine residue in a homeodomain generates dominant negative thyroid transcription factor 1
Mutation of luxS of Streptococcus pneumoniae affects virulence in a mouse model
Mutational analysis of allylic substrate binding site of Micrococcus luteus B-P 26 undecaprenyl diphosphate synthase
Mutation rate and novel tt mutants of Arabidopsis thaliana induced by carbon
Mutation of interfacial residues disrupts subunit folding and particle assembly of Physalis mottle tymovirus
Mutagenic specificity of model estrogen - DNA adducts in mammalian cells
Mutagenesis of the fructose-6-phosphate-binding site in the 2-kinase domain of 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase
Mutations in the N- and D-helices of the N-domain of troponin C affect the C-domain and regulatory function
Mutational specificity in a shuttle vector replicating in chromium(VI)-treated mammalian cells
Mutational analysis clopidogrel resistance and platelet function in patients scheduled for coronary artery bypass grafting
Mutation analysis of K-ras and beta-catenin genes related to O-6-methylguanin-DNA methyltransferase and mismatch repair protein status in human gallbladder carcinoma
Mutations in the murine erythroid alpha-spectrin gene alter spectrin mRNA and protein levels and spectrin incorporation into the red blood cell membrane skeleton
Mutational analysis of a conserved signal-transducing element: the HAMP linker of the Escherichia coli nitrate sensor NarX
Mutagenicity and genotoxicity of the mycotoxin ochratoxin A
Mutagenic spectrum of butadiene-derived N1-deoxyinosine adducts and N-6,N-6-deoxyadenosine intrastrand cross-links in mammalian cells
Mutational hotspots in the LAMB3 gene in the lethal (Herlitz) type of junctional epidermolysis bullosa
Mutational analysis of mismatch repair genes, hMLH1 and hMSH2, in sporadic endometrial carcinomas with microsatellite instability
Mutational analysis of era, an essential GTP-binding protein of Escherichia coli
Mutation in the lysA gene impairs the symbiotic properties of Mesorhizobium ciceri
Mutation or Loss of p53 Differentially Modifies TGF beta Action in Ovarian Cancer
Mutational spectrum of the APC and MUTYH genes and genotype-phenotype correlations in Brazilian FAP, AFAP, and MAP patients
Mutational analysis of yeast mitochondrial translational activator Cbs2p and of YHR063Cp, a protein with similarity to Cbs2p
Mutation analysis of the 5 ' untranslated region of the cold shock cspA mRNA of Escherichia coli
Mutations in COL27A1 cause Steel syndrome and suggest a founder mutation effect in the Puerto Rican population
Mutation of the conserved polyadenosine RNA binding protein, ZC3H14/dNab2, impairs neural function in Drosophila and humans
Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadism
Mutation spectrum of MLL2 in a cohort of kabuki syndrome patients
Mutagenicity, toxicity and repair of DNA base damage induced by oxidation
Mutagenicity of 5-formylcytosine, an oxidation product of 5-methylcytosine, in DNA in mammalian cells
Mutational analysis reveals that an array of GCAAG/CTTGC motifs between sprit promoter sequences for RNA polymerase III is essential for neural BC1 RNA transcription
Mutations of the human thyrotropin receptor gene causing thyroid hypoplasia and persistent congenital hypothyroidism
Mutated barley (1,3)-beta-D-glucan endohydrolases synthesize crystalline (1,3)-beta-D-glucans
Mutations in the embB locus among Korean clinical isolates of Mycobacterium tuberculosis resistant to ethambutol
Mutational analysis of bacteriophage T4 AsiA: involvement of N- and C-terminal regions in binding to sigma(70) of Escherichia coli in vivo
Mutations in sdh (succinate dehydrogenase genes) alter the thiamine requirement of Salmonella typhimurium
Mutation-specific antibody detects mutant BRAF(V600E) protein expression in human colon carcinomas
Mutation of epidermal growth factor receptor is associated with MIG6 expression
Mutations altering the cleavage specificity of a homing endonuclease
Mutational analysis of the transcriptional regulator GcvA: Amino acids important for activation, repression, and DNA binding
Mutational analysis of the active site of Pseudomonas fluorescens pyrrolidone carboxyl peptidase
Mutational analyses of the extracellular domain of the full-length lutropin/choriogonadotropin receptor suggest leucine-rich repeats 1-6 are involved in hormone binding
Mutations of ras genes are relatively frequent in Japanese prostate cancers: Pointing to genetic differences between populations
Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus
Mutation Analysis of the ERCC4/FANCQ Gene in Hereditary Breast Cancer
Mutation in the carboxy-terminal propeptide of the Pro alpha 1(1) chain of type I collagen in a child with severe osteogenesis imperfecta (OI type III): Possible implications for protein folding
Mutational analysis of capping protein function in Saccharomyces cerevisiae
Mutant chaperonin proteins: new tools for nanotechnology
Mutation landscape in melanoma patients clinical implications of heterogeneity of BRAF mutations
Mutation patterns of mtDNA: Empirical inferences for the coding region
Mutagenesis disrupts posttranslational processing of the Na,K-ATPase catalytic subunit
Mutagenic analysis of Vav reveals that an intact SH3 domain is required for transformation
Mutagenic specificity of (Acetylamino)fluorene-derived DNA adducts in mammalian cells
Mutations of the withered (whd) gene in Drosophila melanogaster confer hypersensitivity to oxidative stress and are lesions of the carnitine palmitoyltransferase I (CPT I) gene
Mutation analysis of the histidine residues in the glycylglycine endopeptidase ALE-1
Mutations Associated with Beta-Thalassemia intermedia in Kuwait
Mutagenic potential of benzo[a] pyrene-derived DNA adducts positioned in codon 273 of the human P53 gene
Mutagenic properties of 3-(deoxyguanosin-N-2-yl)-2-acetylaminofluorene, a persistent acetylaminofluorene-derived DNA adduct in mammalian cells
Mutational hot spots in the mitochondrial microcosm
Mutational analysis of the hepatitis C virus RNA helicase
Mutation Gln(54)Leu of the conserved polar residue in the interfacial coiled coil position (d) results in significant stabilization of the original structure of the COMP pentamerization domain
Mutagenesis of residue 157 in the active site of human glyoxalase I
Mutants affected in the putative diacylglycerol binding site of yeast protein kinase C
Mutations in the dihydrofolate reductase gene of trimethoprim-resistant isolates of Streptococcus pneumoniae
Mutation analysis of the purine operon leader region in Bacillus subtilis
Mutagenesis of photosystem I in the region of the ferredoxin cross-linking site: Modifications of positively charged amino acids
Mutagenesis of three surface-exposed loops of a Bacillus thuringiensis insecticidal toxin reveals residues important for toxicity, receptor recognition and possibly membrane insertion
Mutations in the TSGA14 gene in Families With Autism Spectrum Disorders
Mutations of the RNase HC helix of the Moloney murine leukemia virus reverse transcriptase reveal defects in polypurine tract recognition
Mutational analysis of the tRNA(3)(Lys)/HIV-1 RNA (primer/template) complex
Mutations in both the U5 region and the primer-binding site influence the selection of the tRNA used for the initiation of HIV-1 reverse transcription
Mutational analysis of the catalytic subunit of the yeast vacuolar proton-translocating ATPase
Mutational and DNA binding specificity of the carcinogen 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline
Mutational analysis of RNA structures and sequences postulated to affect 3' processing of M1 RNA, the RNA component of Escherichia coli RNase P
Mutations in the yeast SRB2 general transcription factor suppress hpr1-induced recombination and show defects in DNA repair
Mutagenic potential of alpha-(N2-deoxyguanosinyl)tamoxifen lesions, the major DNA adducts detected in endometrial tissues of patients treated with tamoxifen
Mutation of an active site residue in Escherichia coli uracil-DNA glycosylase: Effect on DNA binding, uracil inhibition and catalysis
Mutations in the nucleolar proteins Tma23 and Nop6 suppress the malfunction of the Nep1 protein
Mutational changes in S-cone opsin genes common to both nocturnal and cathemeral Aotus monkeys
Mutants that show increased sensitivity to hydrogen peroxide reveal an important role for the pentose phosphate pathway in protection of yeast against oxidative stress
Mutational analysis of the CitA citrate transporter from Salmonella typhimurium: Altered substrate specificity
Mutated myocilin and heterozygous Sod2 deficiency act synergistically in a mouse model of open-angle glaucoma
Mutational analysis and molecular modelling of an amino acid sequence motif conserved in antiporters but not symporters in a transporter superfamily
Mutational analysis of U1 function in Schizosaccharomyces pombe: Pre-mRNAs differ in the extent and nature of their requirements for this snRNA in vivo
Mutation of TP53 and Alteration of p14(arf) Expression in EGFR- and KRAS-Mutated Lung Adenocarcinomas
Mutational analysis of the N-linked glycosylation sites of the human insulin receptor
Mutants of the lactose carrier of Escherichia coli which show altered sugar recognition plus a severe defect in sugar accumulation
Mutational analysis of a fatty acyl-coenzyme A synthetase signature motif identifies seven amino acid residues that modulate fatty acid substrate specificity
Mutational studies with Atp12p, a protein required for assembly of the mitochondrial F-1-ATPase in yeast - Identification of domains important for Atp12p function and oligomerization
Mutations in the MDR3 gene cause progressive familial intrahepatic cholestasis
Mutational analysis of the catalytic centre of the Citrobacter freundii AmpD N-acetylmuramyl-L-alanine amidase
Mutation analysis of the TGFBI gene in Vietnamese with granular and avellino corneal dystrophy
Mutational analysis of the NIa protease from pepper vein banding potyvirus
Mutational spectrum of NSDHL in CHILD syndrome
Mutation frequencies for glycogen storage disease Ia in the Ashkenazi Jewish population
Mutational Dynamics of Aroid Chloroplast Genomes
Mutations in U5 snRNA loop 1 influence the splicing of different genes in vivo
Mutation detection in the med and med(J) alleles of the sodium channel Scn8a - Unusual splicing due to a minor class AT-AC intron
Mutant Copper-Zinc Superoxide Dismutase (SOD1) Induces Protein Secretion Pathway Alterations and Exosome Release in Astrocytes IMPLICATIONS FOR DISEASE SPREADING AND MOTOR NEURON PATHOLOGY IN AMYOTROPHIC LATERAL SCLEROSIS
Mutation-specific cystic fibrosis treatments on verge of approval
Mutant PrPCJD prevails over wild-type PrPCJD in the brain of V210I and R208H genetic Creutzfeldt-Jakob disease patients
Mutation in murine coronavirus replication protein nsp4 alters assembly of double membrane vesicles
Mutation-selection equilibrium in games with multiple strategies
Mutational analysis of Arabidopsis chloroplast polynucleotide phosphorylase reveals roles for both RNase PH core domains in polyadenylation, RNA 3 '-end maturation and intron degradation
Mutations at the monomer-monomer interface away from the active site of influenza B virus neuraminidase reduces susceptibility to neuraminidase inhibitor drugs
Mutations in IDH1 and IDH2 are not present in sporadic ovarian sex cord-stromal tumours
Mutational analysis of PIK3CA, JAK2, BRAF, FOXL2, IDH1, AKT1 and EZH2 oncogenes in sarcomas
Mutational probing of the forkhead domain of the transcription factor FOXL2 provides insights into the pathogenicity of naturally occurring mutations
Mutational analysis of GCMB, a parathyroid-specific transcription factor, in parathyroid adenoma of primary hyperparathyroidism
Mutational Analysis (c.402C > G) of the FOXL2 Gene and Immunohistochemical Expression of the FOXL2 Protein in Testicular Adult Type Granulosa Cell Tumors and Incompletely Differentiated Sex Cord Stromal Tumors
Mutation spectrum of Fork-Head Transcriptional Factor Gene (FOXL2) in Indian Blepharophimosis Ptosis Epicanthus Inversus Syndrome (BPES) patients
Mutations of the SF3B1 splicing factor in chronic lymphocytic leukemia: association with progression and fludarabine-refractoriness
Mutation of a Broadly Conserved Operon (RL3499-RL3502) from Rhizobium leguminosarum Biovar viciae Causes Defects in Cell Morphology and Envelope Integrity
Mutational and Structural Studies of the PixD BLUF Output Signal That Affects Light-Regulated Interactions with PixE
Mutations in Frizzled 6 Cause Isolated Autosomal-Recessive Nail Dysplasia
Mutations in GTPBP3 Cause a Mitochondria! Translation Defect Associated with Hypertrophic Cardiomyopathy, Lactic Acidosis, and Encephalopathy
Mutation in the mitochondrial translation elongation factor EFTs results in severe infantile liver failure
Mutations of the Mitochondrial-tRNA Modifier MTO1 Cause Hypertrophic Cardiomyopathy and Lactic Acidosis
Mutation in PNPT1, which Encodes a Polyribonucleotide Nucleotidyltransferase, Impairs RNA Import into Mitochondria and Causes Respiratory-Chain Deficiency
Mutation in mitochondrial ribosomal protein MRPS22 leads to Cornelia de Lange-like phenotype, brain abnormalities and hypertrophic cardiomyopathy
Mutation of essential Hsp90 co-chaperones SGT1 or CNS1 renders yeast hypersensitive to overexpression of other co-chaperones
Mutant Pink1 induces mitochondrial dysfunction in a neuronal cell model of Parkinson's disease by disturbing calcium flux
Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)
Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores
Mutagenesis of Conserved Amino Acids of Helicobacter pylori Fur Reveals Residues Important for Function
Mutations associated with Charcot-Marie-Tooth disease cause SIMPLE protein mislocalization and degradation by the proteasome and aggresome-autophagy pathways
Mutations in the Testis-Specific Enhancer of SOX9 in the SRY Independent Sex-Determining Mechanism in the Genus Tokudaia
Mutations in MMP9 and MMP13 Determine the Mode of Inheritance and the Clinical Spectrum of Metaphyseal Anadysplasia
Mutations in C12orf57 Cause a Syndromic Form of Colobomatous Microphthalmia
Mutant Huntingtin Affects Cortical Progenitor Cell Division and Development of the Mouse Neocortex
Mutations in the glucose-6-phosphatase-alpha (G6PC) gene that cause type Ia glycogen storage disease
Mutascope: sensitive detection of somatic mutations from deep amplicon sequencing
Mutations of EFHC1, linked to juvenile myoclonic epilepsy, disrupt radial and tangential migrations during brain development
Mutagenic analysis in a pure molecular system shows that thioredoxin-interacting protein residue Cys247 is necessary and sufficient for a mixed disulfide formation with thioredoxin
Mutations in the CYP1B1 gene may contribute to juvenile-onset open-angle glaucoma
Mutation of a nicotinic acetylcholine receptor beta subunit is associated with resistance to neonicotinoid insecticides in the aphid Myzus persicae
Mutations in KIF7 link Joubert syndrome with Sonic Hedgehog signaling and microtubule dynamics
Mutations affecting the activity of the cyclodextrin glucanotransferase of Paenibacillus pabuli US132: insights into the low hydrolytic activity of cyclodextrin glucanotransferases
Mutagenic and genotoxic activity of particulate matter PM2.5 from Cucuta, Colombia
Mutants of protein kinase A that mimic the ATP-binding site of Aurora kinase
Mutation Screening of the Kruppel-Like Factor 1 Gene Using Single-Strand Conformational Polymorphism in a Cohort of Iranian beta-Thalassemia Patients
Mutations in Twinkle primase-helicase cause Perrault syndrome with neurologic features
Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy
Mutators in cystic fibrosis chronic lung infection: Prevalence, mechanisms, and consequences for antimicrobial therapy
Mutations in TPRN Cause a Progressive Form of Autosomal-Recessive Nonsyndromic Hearing Loss
Mutational analysis of TYR gene and its structural consequences in OCA1A
Mutational Analysis of the TYR and OCA2 Genes in Four Chinese Families with Oculocutaneous Albinism
Mutations to a glycine loop in the catalytic site of human Lon changes its protease, peptidase and ATPase activities
Mutation of nfxB Causes Global Changes in the Physiology and Metabolism of Pseudomonas aeruginosa
Mutational analysis of the inactivating factors, IF7 and IF17 from Synechocystis sp PCC 6803: critical role of arginine amino acid residues for glutamine synthetase inactivation
Mutational Analysis of the Cyanobacterial Nitrogen Regulator PipX
Mutated HLA-G3 localizes to the cell surface but does not inhibit cytotoxicity of natural killer cells
Mutation Frequency and Spectrum of Mutations Vary at Different Chromosomal Positions of Pseudomonas putida
Mutational profiles of different macroscopic subtypes of colorectal adenoma reveal distinct pathogenetic roles for KRAS, BRAF and PIK3CA
Mutations affecting the stability of the haemagglutinin molecule impair the immunogenicity of live attenuated H3N2 intranasal influenza vaccine candidates lacking NS1
Mutations in Traf3ip1 reveal defects in ciliogenesis, embryonic development, and altered cell size regulation
Mutational analysis of ten Turkish patients with glycogen storage disease type III: identification of four novel mutations
Mutations in the Arabidopsis Homolog of LST8/G beta L, a Partner of the Target of Rapamycin Kinase, Impair Plant Growth, Flowering, and Metabolic Adaptation to Long Days
Mutant p53 subverts p63 control over KLF4 expression in keratinocytes
Mutations in AEC syndrome skin reveal a role for p63 in basement membrane adhesion, skin barrier integrity and hair follicle biology
Mutations in LTBP4 Cause a Syndrome of Impaired Pulmonary, Gastrointestinal, Genitourinary, Musculoskeletal, and Dermal Development
Mutational spectrum of CDKL5 in early-onset encephalopathies: a study of a large collection of French patients and review of the literature
Mutation screening of the CDKL5 gene in cryptogenic infantile intractable epilepsy and review of clinical sensitivity
Mutation analysis in Bardet-Biedl syndrome by DNA pooling and massively parallel resequencing in 105 individuals
Mutant Huntingtin Causes Metabolic Imbalance by Disruption of Hypothalamic Neurocircuits
Mutations of POLR3A Encoding a Catalytic Subunit of RNA Polymerase Pol III Cause a Recessive Hypomyelinating Leukodystrophy
Mutant pfcrt %26quot;SVMNT%26quot; haplotype and wild type pfmdr1 %26quot;N86%26quot; are endemic in Plasmodium vivax dominated areas of India under high chloroquine exposure
Mutational analysis of the AtNUDT7 Nudix hydrolase from Arabidopsis thaliana reveals residues required for protein quarternary structure formation and activity
Mutagenic and antimutagenic potentials of fruit juices of five medicinal plants in Allium cepa L.: Possible influence of DPPH free radical scavengers
Mutagenic and antimutagenic assessment of methanol leaf extract of Myristica fragrans (Houtt.) using in vitro and in vivo genetic assays
Mutational Analysis of Pneumocystis jirovecii Dihydropteroate Synthase and Dihydrofolate Reductase Genes in HIV-Infected Patients in China
Mutation-specific IDH1 antibody differentiates oligodendrogliomas and oligoastrocytomas from other brain tumors with oligodendroglioma-like morphology
Mutations of a Country: A Mutation Review of Single Gene Disorders in the United Arab Emirates (UAE)
Mutations galore in myeloproliferative neoplasms: Would the real Spartacus please stand up?
Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsies
Mutational Inactivation of the Nijmegen Breakage Syndrome Gene (NBS1) in Glioblastomas Is Associated With Multiple TP53 Mutations
Mutations in the gyrA and parC genes of quinolone-resistant Neisseria gonorrhoeae isolates in India
Mutational Analysis Reveals the FUS Homolog TAF15 as a Candidate Gene for Familial Amyotrophic Lateral Sclerosis
Mutation of pescadillo Disrupts Oligodendrocyte Formation in Zebrafish
Mutant Thyroid Hormone Receptors (TRs) Isolated from Distinct Cancer Types Display Distinct Target Gene Specificities: A Unique Regulatory Repertoire Associated with Two Renal Clear Cell Carcinomas
Mutations in G6PC2 do not contribute to monogenic forms of early infancy diabetes and beta cell dysfunction
Mutation of the CgPDR16 gene attenuates azole tolerance and biofilm production in pathogenic Candida glabrata
Mutation analysis of BRAF exon 15 and KRAS codons 12 and 13 in Moroccan patients with colorectal cancer
Mutations in precore/basal core promoter regions and viral polymerase in patients with chronic hepatitis B
Mutation frequency is not elevated in the cerebellum of harlequin/Big Blue (R) mice but Class II deletions occur preferentially in young harlequin cerebellum
Mutational spectrum and therapy response of metastasized GIST in Central Switzerland - A population-based study
Mutations in the Arabidopsis homoserine kinase gene DMR1 confer enhanced resistance to Fusarium culmorum and F-graminearum
Mutations that alter the equilibrium between open and closed conformations of Escherichia coli maltose-binding protein impede its ability to enhance the solubility of passenger proteins
Mutation of Ser-50 and Cys-66 in Snapin Modulates Protein Structure and Stability
Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia
Mutant Malonyl-CoA Synthetases with Altered Specificity for Polyketide Synthase Extender Unit Generation
Mutation in ribosomal protein S5 leads to spectinomycin resistance in Neisseria gonorrhoeae
Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood
Mutational analysis of a phenazine biosynthetic gene cluster in Streptomyces anulatus 9663
Mutational and Structural Analysis of L-N-Carbamoylase Reveals New Insights into a Peptidase M20/M25/M40 Family Member
Mutations in Lyar and p53 are synergistically lethal in female mice
Mutagenic analysis of six disinfection by-products in the Tk gene of mouse lymphoma cells
Mutated hilltop inflation: a natural choice for early universe
Mutator activity induced by microRNA-155 (miR-155) links inflammation and cancer
Mutations in growth factor independent-1 associated with human neutropenia mock murine granulopoiesis through colony stimulating factor-1
Mutagenesis of RpoE-like sigma factor genes in Bdellovibrio reveals differential control of groEL and two groES genes
Mutagenic probes of the role of Ser209 on the cavity shaping loop of human monoamine oxidase A
Mutagenesis of tryptophan199 suggests that hopping is required for MauG-dependent tryptophan tryptophylquinone biosynthesis
Mutation rate estimates for 110 Y-chromosome STRs combining population and father-son pair data
Mutations of NOTCH1, FBXW7, and prognosis in T-lineage acute lymphoblastic leukemia
Mutations in BRAF correlate with poor survival of colorectal cancers in Chinese population
Mutant ubiquitin (UBB+1) associated with neurodegenerative disorders is hydrolyzed by ubiquitin C-terminal hydrolase L3 (UCH-L3)
Mutational process in protein-coding genes of human mitochondrial genome in context of evolution of Homo genus
Mutations in the transmembrane and juxtamembrane domains enhance IL27R transforming activity
Mutational analysis of YgfZ, a folate-dependent protein implicated in iron/sulphur cluster metabolism
Mutagenesis of Human Immunodeficiency Virus Reverse Transcriptase p51 Subunit Defines Residues Contributing to Vinylogous Urea Inhibition of Ribonuclease H Activity
Mutant SOD1 forms ion channel: Implications for ALS pathophysiology
Mutations in NOTCH3 cause the formation and retention of aggregates in the endoplasmic reticulum, leading to impaired cell proliferation
Mutational analysis of putative phosphate- and proton-binding sites in the Saccharomyces cerevisiae Pho84 phosphate:H+ transceptor and its effect on signalling to the PKA and PHO pathways
Mutations in the Fusion Protein Cleavage Site of Avian Paramyxovirus Serotype 4 Confer Increased Replication and Syncytium Formation In Vitro but Not Increased Replication and Pathogenicity in Chickens and Ducks
Mutations in PMCA2 and hereditary deafness: A molecular analysis of the pump defect
Mutations in exons 5, 7 and 8 of the human voltage-dependent anion channel type 3 (VDAC3) gene in sperm with low motility
Mutational screening and zebrafish functional analysis of GIGYF2 as a Parkinson-disease gene
Mutations in the gene EML1 / EMl1, neuronal progenitors and heterotopias in humans and mice
Mutation-selection equilibrium in games with mixed strategies
Mutation of the fucose-specific beta 1,3 N-acetylglucosaminyltransferase LFNG results in abnormal formation of the spine
Mutant GNAS detected in duodenal collections of secretin-stimulated pancreatic juice indicates the presence or emergence of pancreatic cysts
Mutational patterns in the frameshift-regulating site of HIV-1 selected by protease inhibitors
Mutation in the S-ribosylhomocysteinase (luxS) gene involved in quorum sensing affects biofilm formation and virulence in a clinical isolate of Aeromonas hydrophila
Mutation of a putative S-nitrosylation site of TRPV4 protein facilitates the channel activates
Mutations in IRGM Are Associated With More Frequent Need for Surgery in Patients With Ileocolonic Crohn's Disease
Mutational Analysis of Progesterone Receptor Functional Domains in Stable Cell Lines Delineates Sets of Genes Regulated by Different Mechanisms
Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration
Mutations in the RAM network confer resistance to the thiol oxidant 4,4'-dipyridyl disulfide
Mutant Human Embryonic Stem Cells Reveal Neurite and Synapse Formation Defects in Type 1 Myotonic Dystrophy
Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans
Mutation spectra of the surface-protein-coding region of the HBV genome in HBV-vaccinated and non-vaccinated individuals in Hungary
Mutation analysis of CRYAA, CRYGC, and CRYGD associated with autosomal dominant congenital cataract in Brazilian families
Mutations in Human alpha A-Crystallin/sHSP Affect Subunit Exchange Interaction with alpha B-Crystallin
Mutations/polymorphisms in a monogenetic autoinflammatory disease may be susceptibility markers for certain rheumatic diseases: lessons from the bedside for the benchside
Mutant Wilms' tumor 1 (WT1) mRNA with premature termination codons in acute myeloid leukemia (AML) is sensitive to nonsense-mediated RNA decay (NMD)
Mutational spectrum at GATA1 provides insights into mutagenesis and leukemogenesis in Down syndrome
Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome
Mutation Update: The Spectra of Nebulin Variants and Associated Myopathies
Mutational analysis of FUS gene and its structural and functional role in amyotrophic lateral sclerosis 6
Mutation Spectrum of Meckel Syndrome Genes: One Group of Syndromes or Several Distinct Groups?
Mutations in RPGRIP1L: extending the clinical spectrum of ciliopathies
Mutations of the CEP290 gene encoding a centrosomal protein cause Meckel-Gruber syndrome
Mutational analysis of the RPGRIP1L gene in patients with Joubert syndrome and nephronophthisis
Mutation analysis of NPHP6/CEP290 in patients with Joubert syndrome and Senior-Loken syndrome
Mutations in MYB3R1 and MYB3R4 Cause Pleiotropic Developmental Defects and Preferential Down-Regulation of Multiple G2/M-Specific Genes in Arabidopsis
Mutation detection in DNA isolated from cerebrospinal fluid and urine: Clinical utility and pitfalls of multiple displacement amplification
Mutant HFE H63D Protein Is Associated with Prolonged Endoplasmic Reticulum Stress and Increased Neuronal Vulnerability
Mutations of the SYCP3 Gene in Women with Recurrent Pregnancy Loss
Mutations in the Nebulin Gene in a Child with Nemaline (Rod) Myopathy
Mutation of PEB4 alters the outermembrane protein profile of Campylobacter jejuni
Mutational analysis of domain antibodies reveals aggregation hotspots within and near the complementarity determining regions
Mutation analysis of the C1QTNF3 gene in patients with schizophrenia
Mutation V111I in HIV-2 Reverse Transcriptase Increases the Fitness of the Nucleoside Analogue-Resistant K65R and Q151M Viruses
Mutant presenilin-1 deregulated peripheral immunity exacerbates Alzheimer-like pathology
Mutations and/or close relatives? Six case work examples where 49 autosomal SNPs were used as supplementary markers
Mutational analysis of TAC3 and TACR3 genes in patients with idiopathic central pubertal disorders
Mutations in FUS cause FALS and SALS in French and French Canadian populations
Mutational analysis of FANCL, FANCM and the recently identified FANCI suggests that among the 13 known Fanconi Anemia genes, only FANCD1/BRCA2 plays a major role in high-risk breast cancer predisposition
Mutations in the fks1 gene in Candida albicans, C-tropicalis, and C-krusei correlate with elevated caspofungin MICs uncovered in AM3 medium using the method of the European Committee on Antibiotic Susceptibility Testing
Mutation update on the CHD7 gene involved in CHARGE syndrome
Mutation analysis in primary immunodeficiency diseases: case studies
Mutations along the hypothalamic-pituitary-gonadal axis affecting male reproduction
Mutational and In Silico Analyses for Antidepressant Block of Astroglial Inward-Rectifier Kir4.1 Channel
Mutational analysis of ABC proteins
Mutated K-rasAsp12 promotes tumourigenesis in ApcMin mice more in the large than the small intestines, with synergistic effects between K-ras and Wnt pathways
Mutational analysis of EZH2 codon 641 in non-Hodgkin lymphomas and leukemias
Mutations in alpha- and beta-tubulin encoding genes: Implications in brain malformations
Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria
Mutation and polymorphism spectrum in osteogenesis imperfecta type II: implications for genotype-phenotype relationships
Mutations in patients with osteogenesis imperfecta from consanguineous Indian families
Mutant human beta 4 subunit identified in amyotrophic lateral sclerosis patients impairs nicotinic receptor function
Mutations in Streptococcus pneumoniae Penicillin-Binding Protein 2x: Importance of the C-Terminal Penicillin-Binding Protein and Serine/Threonine Kinase-Associated Domains for Beta-Lactam Binding
Mutation-specific control of BCR-ABL T3151 positive leukemia with a recombinant yeast-based therapeutic vaccine in a murine model
Mutations in the neuronal beta-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defects
Mutations of the Gene for the Aryl Hydrocarbon Receptor-Interacting Protein in Pituitary Adenomas
Mutations in the FOG2/ZFPM2 gene are associated with anomalies of human testis determination
Mutational analysis of residues in the regulatory CBS domains of Moorella thermoacetica pyrophosphatase corresponding to disease-related residues of human proteins
Mutant epidermal growth factor receptor vlll increases cell motility and clonogenecity in a prostate cell line RWPE1
Mutation in the transcriptional regulator phol? contributes to avirulence of Mycobacterium tuberculosis H37Ra strain
Mutational 'hot-spots' in mammalian, bacterial and protozoal dihydrofolate reductases associated with antifolate resistance: Sequence and structural comparison
Mutant MMP-9 and HGF Gene Transfer Enhance Resolution of CCl4-Induced Liver Fibrosis in Rats: Role of ASH1 and EZH2 Methyltransferases Repression
Mutations in the Catalytic Domain of Human Matrix Metalloproteinase-1 (MMP-1) That Allow for Regulated Activity through the Use of Ca2+
Mutations in Phosphoinositide Metabolizing Enzymes and Human Disease
Mutations in VLDLR as a Cause for Autosomal Recessive Cerebellar Ataxia With Mental Retardation (Dysequilibrium Syndrome)
Mutation of megalin leads to urinary loss of selenoprotein P and selenium deficiency in serum, liver, kidneys and brain
Mutations in JPH2-encoded junctophilin-2 associated with hypertrophic cardiomyopathy in humans
Mutations in MAB21L2 Result in Ocular Coloboma, Microcornea and Cataracts
Mutation T74S in HIV-1 subtype B and C proteases resensitizes them to ritonavir and indinavir and confers fitness advantage
Mutagenic roles of DNA "repair" proteins in antibody diversity and disease-associated trinucleotide repeat instability
Mutated response regulator graR is responsible for phenotypic conversion of Staphylococcus aureus from heterogeneous vancomycin-intermediate resistance to vancomycin-intermediate resistance
Mutations in the human SC4MOL gene encoding a methyl sterol oxidase cause psoriasiform dermatitis, microcephaly, and developmental delay
Mutational analysis of the LDL receptor and APOB genes in Mexican individuals with autosomal dominant hypercholesterolemia
Mutant p53 Disrupts Mammary Tissue Architecture via the Mevalonate Pathway
Mutation in porcine Zip4-like zinc transporter is associated with pancreatic zinc concentration and apparent zinc absorption
Mutagenesis studies of neuropeptide S identify a suitable peptide tracer for neuropeptide S receptor binding studies and peptides selectively activating the I-107 variant of human neuropeptide S receptor
Mutations in the aryl hydrocarbon receptor interacting protein gene are not highly prevalent among subjects with sporadic pituitary adenomas
Mutation screening of AURKB and SYCP3 in patients with reproductive problems
Mutation rates at Y chromosome short tandem repeats in Texas populations
Mutation rate at 17 Y-STR loci in "Father/Son" pairs from moroccan population
Mutant AKT1 in Proteus Syndrome REPLY
Mutational analysis of Cys(88) of Toll-like receptor 4 highlights the critical role of MD-2 in cell surface receptor expression
Mutational analysis of amino acid residues involved in IgE-binding to the Malassezia sympodialis allergen Mala s 11
Mutations defective in ribonucleotide reductase activity interfere with pollen plastid DNA degradation mediated by DPD1 exonuclease
Mutational Evidence for a Structural Model of the Lassa Virus RNA Polymerase Domain and Identification of Two Residues, Gly1394 and Asp1395, That Are Critical for Transcription but Not Replication of the Genome
Mutations of KRAS and TP53 in a Minor Proportion of Opisthorchis viverrini-Associated Cholangiocarcinomas in a Hamster Model
Mutations in pattern recognition receptor genes modulate seroreactivity to microbial antigens in patients with inflammatory bowel disease
Mutations in C8orf37, Encoding a Ciliary Protein, are Associated with Autosomal-Recessive Retinal Dystrophies with Early Macular Involvement
Mutation Survey of Known LCA Genes and Loci in the Saudi Arabian Population
Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in Southern India
Mutations in SPATA7 Cause Leber Congenital Amaurosis and Juvenile Retinitis Pigmentosa
Mutation analysis of the AATF gene in breast cancer families
Mutations in BRCA2 and PALB2 in male breast cancer cases from the United States
Mutational analysis of the breast cancer susceptibility gene BRIP1 /BACH1/FANCJ in high-risk non-BRCA1/BRCA2 breast cancer families
Mutation Studies in the CFTR Gene in Asian Indian Subjects with Congenital Bilateral Absence of Vas Deferens: Report of Two Novel Mutations and Four Novel Variants
Mutations in exon 12 of JAK2 are mainly found in JAK2 V617F-negative polycythaemia vera patients
Mutational, inhibitory and microcalorimetric analyses of Plasmodium falciparum TMP kinase. Implications for drug discovery
Mutational Analysis of Mycobacterium UvrD1 Identifies Functional Groups Required for ATP Hydrolysis, DNA Unwinding, and Chemomechanical Coupling
Mutation of the Wilms' Tumor 1 Gene Is a Poor Prognostic Factor Associated With Chemotherapy Resistance in Normal Karyotype Acute Myeloid Leukemia: The United Kingdom Medical Research Council Adult Leukaemia Working Party
Mutation at the cargo-receptor binding site of Atg8 also affects its general autophagy regulation function
Mutations in MEOX1, Encoding Mesenchyme Homeobox 1, Cause Klippel-Feil Anomaly
Mutations of CXorf6 are associated with a range of severities of hypospadias
Mutations affecting the oligomerization interface of G-protein-coupled receptors revealed by a novel de novo protein design framework
Mutations in the Connexin 29 Gene Are Not a Major Cause of Nonsyndromic Hearing Impairment in India
Mutations M184V and Y115F in HIV-1 Reverse Transcriptase Discriminate against "Nucleotide-competing Reverse Transcriptase Inhibitors"
Mutations in the nervous system-specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II
Mutations in ADAR1, IFIH1, and RNASEH2B Presenting As Spastic Paraplegia
Mutations involved in Aicardi-Goutieres syndrome implicate SAMHD1 as regulator of the innate immune response
Mutation analysis of the genes involved in the Ras-mitogen-activated protein kinase (MAPK) pathway in Korean patients with Noonan syndrome
Mutations in the fifth immunoglobulin-like domain of kit are common and potentially sensitive to imatinib mesylate in feline mast cell tumours
Mutations affecting GABAergic signaling in seizures and epilepsy
Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy
Mutations in amphiphysin 2 (BIN 1) cause outosomal recessive centronuclear myopathy
Mutation at the circadian clock gene EARLY MATURITY 8 adapts domesticated barley (Hordeum vulgare) to short growing seasons
Mutated calreticulin retains structurally disordered C terminus that cannot bind Ca2+: some mechanistic and therapeutic implications
Mutations in PNKD causing paroxysmal dyskinesia alters protein cleavage and stability
Mutational Analysis of N381, a Key Trimer Contact Residue in Tsr, the Escherichia coli Serine Chemoreceptor
Mutational analyses of HAMP helices suggest a dynamic bundle model of input-output signalling in chemoreceptors
Mutational analysis of the connector segment in the HAMP domain of Tsr, the Escherichia coli serine chemoreceptor
Mutation spectrum of 122 hemophilia A families from Taiwanese population by LD-PCR, DHPLC, multiplex PCR and evaluating the clinical application of HRM
Mutagenic and recombinagenic responses to defective DNA polymerase delta are facilitated by the Rev1 protein in pol3-t mutants of Saccharomyces cerevisiae
Mutant WDR36 directly affects axon growth of retinal ganglion cells leading to progressive retinal degeneration in mice
Mutagenicity and cytotoxicity in patients submitted to ionizing radiation A comparison between cone beam computed tomography and radiographs for orthodontic treatment
Mutational analysis of the eyeless gene and phenotypic rescue reveal that an intact Eyeless protein is necessary for normal eye and brain development in Drosophila
Mutagenesis and computer modeling studies of a GPCR conserved residue W5.43(194) in ligand recognition and signal transduction for CB2 receptor
Mutations in the SORT1 gene are unlikely to cause autosomal dominant hypercholesterolemia
Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies
Mutations in the paralogous human alpha-globin genes yielding identical hemoglobin variants
Mutant surfactant A2 proteins associated with familial pulmonary fibrosis and lung cancer induce TGF-beta 1 secretion
Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita
Mutations in the Chromosomal Passenger Complex and the Condensin Complex Differentially Affect Synaptonemal Complex Disassembly and Metaphase I Configuration in Drosophila Female Meiosis
Mutations in nsP1 and PE2 are critical determinants of Ross River virus-induced musculoskeletal inflammatory disease in a mouse model
Mutations of highly conserved bases in the peptidyltransferase center induce compensatory rearrangements in yeast ribosomes
Mutation Patterns in the Human Genome: More Variable Than Expected
Mutational Analysis of Fukutin Gene in Dilated Cardiomyopathy and Hypertrophic Cardiomyopathy
Mutations of the von Hippel-Lindau gene confer increased susceptibility to natural killer cells of clear-cell renal cell carcinoma
Mutations of TSEN and CASK genes are prevalent in pontocerebellar hypoplasias type 2 and 4
Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum (vol 40, pg 1065, 2008)
Mutations in the ExbB Cytoplasmic Carboxy Terminus Prevent Energy-Dependent Interaction between the TonB and ExbD Periplasmic Domains
Mutations in the Sarcomere Gene MYH7 in Ebstein Anomaly
Mutations in ALDH1A3 cause microphthalmia
Mutants of the Base Excision Repair Glycosylase, Endonuclease III: DNA Charge Transport as a First Step in Lesion Detection
Mutant Genetic Background Affects the Functional Rearrangement and Kinetic Properties of JMJD2b Histone Demethylase
Mutated and amplified NRAS in a subset of cutaneous melanocytic lesions with dermal spitzoid morphology: report of two pediatric cases located on the ear
Mutational Inactivation of PTPRD in Glioblastoma Multiforme and Malignant Melanoma
Mutational screening of the USH2A gene in Spanish USH patients reveals 23 novel pathogenic mutations
Mutations That Impact the Enteropathogenic Escherichia coli Cpx Envelope Stress Response Attenuate Virulence in Galleria mellonella
Mutation spectra induced by 1-nitropyrene 4,5-oxide and 1-nitropyrene 9,10-oxide in the supF gene of human XP-A fibroblasts
Mutations in the thumb-connection and RNase H domain of HIV type-1 reverse transcriptase of antiretroviral treatment-experienced patients
Mutations in the Hepatitis C Virus Polymerase that Increase RNA Binding Can Confer Resistance to Cyclosporine A
Mutant Atp13a2 proteins involved in parkinsonism are degraded by ER-associated degradation and sensitize cells to ER-stress induced cell death
Mutation in the substrate-binding site of aminopeptidase B confers new enzymatic properties
Mutations in the Proteolipid Subunits of the Vacuolar H+-ATPase Provide Resistance to Indolotryptoline Natural Products
Mutations in fam20b and xylt1 Reveal That Cartilage Matrix Controls Timing of Endochondral Ossification by Inhibiting Chondrocyte Maturation
Mutations in the JAK2 and MPL Genes and their Correlation to Clinical Parameters in Patients with Chronic Myeloproliferative Disease
Mutagenesis from Meiotic Recombination Is Not a Primary Driver of Sequence Divergence between Saccharomyces Species
Mutations at Several Loci Cause Increased Expression of Ribonucleotide Reductase in Escherichia coli
Mutation Size Optimizes Speciation in an Evolutionary Model
Mutations in PDGFRB and NOTCH3 are the first genetic causes identified for autosomal dominant infantile myofibromatosis
Mutations in the Catalytic Loop HRD Motif Alter the Activity and Function of Drosophila Src64
Mutational spectrum in eight Korean patients with 3-methylcrotonyl-CoA carboxylase deficiency
Mutations in CEP57 cause mosaic variegated aneuploidy syndrome
Mutations of JAK2 and TET2, but not CBL are detectable in a high portion of patients with refractory anemia with ring sideroblasts and thrombocytosis
Mutation mapping and identification by whole-genome sequencing
Mutational screening of EXT1 and EXT2 genes in Polish patients with hereditary multiple exostoses
Mutations in the DNA polymerase and thymidine kinase genes of herpes simplex virus clinical isolates resistant to antiherpetic drugs
Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth
Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance
Mutations in Domain I Interhelical Loops Affect the Rate of Pore Formation by the Bacillus thuringiensis Cry1Aa Toxin in Insect Midgut Brush Border Membrane Vesicles
Mutagenesis in crop improvement under the climate change
Mutation at the folate receptor 4 locus modulates gene expression profiles in the mouse uterus in response to periconceptional folate supplementation
Mutation of L-2,3-diaminopropionic acid synthase genes blocks staphyloferrin B synthesis in Staphylococcus aureus
Mutations in Hepatitis C Virus E2 Located outside the CD81 Binding Sites Lead to Escape from Broadly Neutralizing Antibodies but Compromise Virus Infectivity
Mutant SOD1 G93A microglia have an inflammatory phenotype and elevated production of MCP-1
Mutations in SDHD are the major determinants of the clinical characteristics of Dutch head and neck paraganglioma patients
Mutations in Plasmodium falciparum K13 propeller gene from Bangladesh (2009-2013)
Mutational analysis of CDKN2A gene in a group of 390 larynx cancer patients
Mutation of Y925F in focal adhesion kinase (FAK) suppresses melanoma cell proliferation and metastasis
Mutation screening of the CARD15 gene in sarcoidosis
Mutagenesis of the Bacterial RNA Polymerase Alpha Subunit for Improvement of Complex Phenotypes
Mutated in colorectal cancer, a putative tumor suppressor for serrated colorectal cancer, selectively represses beta-catenin-dependent transcription
Mutations in the neverland Gene Turned Drosophila pachea into an Obligate Specialist Species
Mutagenicity of Immunosuppressive Medications among Renal Transplant Recipients
Mutation spectrum in HNPCC in the Israeli population
Mutator genes giving rise to decreased antibiotic susceptibility in Pseudomonas aeruginosa
Mutation of the H-helix in antithrombin decreases heparin stimulation of protease inhibition
Mutations in the Gene Encoding the Calcium-Permeable Ion Channel TRPV4 Produce Spondylometaphyseal Dysplasia, Kozlowski Type and Metatropic Dysplasia
Mutational analyses of trimethylguanosine synthase (Tgs1) and Mud2: Proteins implicated in pre-mRNA splicing
Mutagenesis of Beryllium-Specific TCRs Suggests an Unusual Binding Topology for Antigen Recognition
Mutant Cockayne syndrome group B protein inhibits repair of DNA topoisomerase I-DNA covalent complex
Mutation rate of VNTR loci in Mycobacterium tuberculosis: Response to Supply et al.
Mutation analysis of the glycerol-3 phosphate dehydrogenase-1 like (GPD1L) gene in Japanese patients with Brugada syndrome
Mutation-, Aging-, and Gene Dosage-dependent Accumulation of Neuroserpin (G392E) in Endoplasmic Reticula and Lysosomes of Neurons in Transgenic Mice
Mutating loops and 2-cycles in 2-CY triangulated categories
Mutation classes of (A)over-tilden-quivers and derived equivalence classification of cluster tilted algebras of type (A)over-tilde(n)
Mutations in Multiple Domains of c-Myb Disrupt Interaction with CBP/p300 and Abrogate Myeloid Transforming Ability
Mutations in Two Zinc-Cluster Proteins Activate Alternative Respiratory and Gluconeogenic Pathways and Restore Senescence in Long-Lived Respiratory Mutants of Podospora anserina
Mutations at human immunodeficiency virus type 1 reverse transcriptase tryptophan repeat motif attenuate the inhibitory effect of efavirenz on virus production
Mutations in the HIV-1 reverse transcriptase tryptophan repeat motif affect virion maturation and Gag-Pol packaging
Mutagenicity and genotoxicity of isatin in mammalian cells in vivo
Mutagenesis of the West Nile virus NS2B cofactor domain reveals two regions essential for protease activity
Mutation of ACTA2 Gene as an Important Cause of Familial and Nonfamilial Nonsyndromatic Thoracic Aortic Aneurysm and/or Dissection (TAAD)
Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections
Mutational analysis of thirty-two double-strand DNA break repair genes in breast and pancreatic cancers
Mutagenic and Genotoxic Effects of cis-(Dichloro)tetraammineruthenium(III) Chloride on Human Peripheral Blood Lymphocytes
Mutations that permit residual CFTR function delay acquisition of multiple respiratory pathogens in CF patients
Mutation of a single allele of the cancer susceptibility gene BRCA1 leads to genomic instability in human breast epithelial cells
Mutations in the RNA Granule Component TDRD7 Cause Cataract and Glaucoma
Mutational analysis of DOK2 tumor suppressor gene in acute leukemias
Mutagenesis of tyrosine and di-leucine motifs in the HIV-1 envelope cytoplasmic domain results in a loss of Env-mediated fusion and infectivity
Mutations in Drosophila Myosin Rod Cause Defects in Myofibril Assembly
Mutations in the PSTPIP1 gene and aberrant splicing variants in patients with pyoderma gangrenosum
Mutations That Hamper Dimerization of Foot-and-Mouth Disease Virus 3A Protein Are Detrimental for Infectivity
Mutants of an electrogenic bacterium Shewanella oneidensis MR-1 with increased reducing activity
Mutations at pipX Suppress Lethality of P-II-Deficient Mutants of Synechococcus elongatus PCC 7942
Mutant A53T alpha-Synuclein Induces Neuronal Death by Increasing Mitochondrial Autophagy
Mutant mouse models and antidepressant drug research: focus on serotonin and brain-derived neurotrophic factor
Mutagenic Effects of Carboplatin on Somatic Cells of Male Albino Mice
Mutation of tyrosine 145 of lymphocyte cytosolic protein 2 protects mice from anaphylaxis and arthritis
Mutations in CIB2 calcium and integrin-binding protein disrupt auditory hair cell calcium homeostasis in Usher syndrome type 1J and non-syndromic deafness DFNB48
Mutation of the Protein Kinase I Alpha Leucine Zipper Domain Produces Hypertension and Progressive Left Ventricular Hypertrophy: A Novel Mouse Model of Age-Dependent Hypertensive Heart Disease
Mutating the Tight-Dimer Interface of Dihydrodipicolinate Synthase Disrupts the Enzyme Quaternary Structure: Toward a Monomeric Enzyme
Mutant CEBPA: Priming Stem Cells for Myeloid Leukemogenesis
Mutation of C/EBP alpha predisposes to the development of myeloid leukemia in a retroviral insertional mutagenesis screen
Mutations in cardiac T-box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiornyopathy
Mutational analysis of beta COP (Sec26p) identifies an appendage domain critical for function
Mutational Biases and Selective Forces Shaping the Structure of Arabidopsis Genes
Mutagenicity of diesel engine exhaust in the Ames/Salmonella assay using a direct exposure method
Mutagenicity and genotoxicity of suspended particulate matter in the Seine river estuary
Mutations in the NOG gene are commonly found in congenital stapes ankylosis with symphalangism, but not in otosclerosis
Mutagenesis of longer inserts by the ligation of two PCR fragments amplified with a mutation primer
Mutation of a Gene Essential for Ribosome Biogenesis, EMG1, Causes Bowen-Conradi Syndrome
Mutation Analysis of the Main Hypertrophic Cardiomyopathy Genes Using Multiplex Amplification and Semiconductor Next-Generation Sequencing
Mutation Profile of JAK2 Transcripts in Patients with Chronic Myeloproliferative Neoplasias
Mutations in JAK2(V617F) homologous domain of JAK genes are uncommon in solid tumors
Mutant molecules of interest in myeloproliferative neoplasms: Introduction
Mutations in UCP2 in Congenital Hyperinsulinism Reveal a Role for Regulation of Insulin Secretion
Mutagenic Potency of MMS-Induced 1meA/3meC Lesions in E. coli
Mutant alpha-galactosidase A with M296I does not cause elevation of the plasma globotriaosylsphingosine level
Mutant lipooligosaccharide-based conjugate vaccine demonstrates a broad-spectrum effectiveness against Moraxella catarrhalis
Mutations in Pol gene of hepatitis B virus in patients with chronic hepatitis B before and after therapy with nucleoside/nucleotide analogues
Mutation scanning of peach floral genes
Mutant Versions of the S. cerevisiae Transcription Elongation Factor Spt16 Define Regions of Spt16 That Functionally Interact with Histone H3
Mutations in WDR62 gene in Pakistani families with autosomal recessive primary microcephaly
Mutation Analysis of the CYP21A2 Gene in the Iranian Population
Mutations in HPSE2 Cause Urofacial Syndrome (vol 86, pg 963, 2010)
Mutagenesis of Surfactant Protein D Informed by Evolution and X-ray Crystallography Enhances Defenses against Influenza A Virus in Vivo
Mutations in Subunit Interface and B-cell Epitopes Improve Antileukemic Activities of Escherichia coli Asparaginase-II EVALUATION OF IMMUNOGENICITY IN MICE
Mutant HSPB1 overexpression in neurons is sufficient to cause age-related motor neuronopathy in mice
Mutation spectrum of the TYR and SLC45A2 genes in patients with oculocutaneous albinism
Mutations in DDX59 Implicate RNA Helicase in the Pathogenesis of Orofaciodigital Syndrome
Mutational analysis of the major soybean UreF paralogue involved in urease activation
Mutational analysis of podocyte genes in children with sporadic steroid-resistant nephrotic syndrome
Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts
Mutation in the Plasmodium falciparum CRT Protein Determines the Stereospecific Activity of Antimalarial Cinchona Alkaloids
Mutation in TTI2 Reveals a Role for Triple T Complex in Human Brain Development
Mutational screening of 320 Brazilian patients with autosomal dominant spinocerebellar ataxia
Mutations in ribosomal proteins and ribosomal RNA confer macrolide resistance in human Ureaplasma spp.
Mutations in gene PVRL4 encoding for cell adhesion molecule Nectin-4 in ectodermal dysplasia-syndactyly syndrome
Mutation in PVRL4 gene encoding nectin-4 underlies ectodermal-dysplasia-syndactyly syndrome (EDSS1)
Mutational analysis of MED12 exon 2 in uterine leiomyoma and other common tumors
Mutational Robustness of Gene Regulatory Networks
Mutation of NPM1 and FLT3 Genes in Acute Myeloid Leukemia and Their Association with Clinical and Immunophenotypic Features
Mutanlallemand (mtl) and Belly Spot and Deafness (bsd) Are Two New Mutations of Lmx1a Causing Severe Cochlear and Vestibular Defects
Mutations in Myosin Light Chain Kinase Cause Familial Aortic Dissections (vol 87, pg 701, 2010)
Mutations in the planar cell polarity gene, Fuzzy, are associated with neural tube defects in humans
Mutations in CDKN2C (p18) and CDKN2D (p19) may cause sporadic parathyroid adenoma
Mutation Vif-22H, which allows HIV-1 to use the APOBEC3G hypermutation to develop resistance, could appear more quickly in certain non-B variants
Mutagenicity and Mutagens of the Red Chili Pepper as Gallbladder Cancer Risk Factor in Chilean Women
Mutational Analysis of 12 Patients With the Phenotype of Ehlers-Danlos Syndrome Type VIB Shows no Linkage to the Zinc Transporter Gene SLC39A13
Mutated RAS and constitutively activated Akt delineate distinct oncogenic pathways, which independently contribute to multiple myeloma cell survival
Mutations in the Escherichia coli Ribosomal Protein L22 Selectively Suppress the Expression of a Secreted Bacterial Virulence Factor
Mutations in the TRPV4 Gene Are Not Associated With Sporadic Progressive Muscular Atrophy
Mutational analysis for GJB2, GJB6, and GJB3 genes in Campania within a universal neonatal hearing screening programme
Mutant CAG repeats of Huntingtin transcript fold into hairpins, form nuclear foci and are targets for RNA interference
Mutation in a primate-conserved retrotransposon reveals a noncoding RNA as a mediator of infantile encephalopathy
Mutant TDP-43 and FUS Cause Age-Dependent Paralysis and Neurodegeneration in C. elegans
Mutations of the SLX4 gene in Fanconi anemia
Mutations in the Planar Cell Polarity Genes CELSR1 and SCRIB are Associated with the Severe Neural Tube Defect Craniorachischisis
Mutations in the Essential Escherichia coli Gene, yqgF, and Their Effects on Transcription
Mutational analysis of the GNA11, MMP27, FGD1, TRRAP and GRM3 genes in thyroid cancer
Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia
Mutation of the TBCE gene causes disturbance of microtubules in the auditory nerve and cochlear outer hair cell degeneration accompanied by progressive hearing loss in the pmn/pmn mouse
Mutations in the EDR1 Gene Alter the Response of Arabidopsis thaliana to Phytophthora infestans and the Bacterial PAMPs fig22 and elf18
Mutations in the PDYN gene (SCA23) are not a frequent cause of dominant ataxia in Central Europe
Mutations in the Antiviral RNAi Defense Pathway Modify Brome mosaic virus RNA Recombinant Profiles
Mutant FUS induces endoplasmic reticulum stress in amyotrophic lateral sclerosis and interacts with protein disulfide-isomerase
Mutational analysis of the proposed calcium-binding aspartates of a truncated alpha-amylase from Bacillus sp strain TS-23
Mutagenesis of Propionibacterium acnes and analysis of two CAMP factor knock-out mutants
Mutation in the senataxin gene found in a patient affected by familial ALS with juvenile onset and slow progression
Mutant JAK3 FERMents ATLL
Mutations of the aurora kinase C gene causing macrozoospermia are the most frequent genetic cause of male infertility in Algerian men
Mutant Kras Promotes Hyperplasia and Alters Differentiation in the Colon Epithelium but Does Not Expand the Presumptive Stem Cell Pool
Mutations in a Dominant Nef Epitope of Simian Immunodeficiency Virus Diminish TCR:Epitope Peptide Affinity but not Epitope Peptide:MHC Class I Binding
Mutant-flu paper published
Mutational hotspots in the mitochondrial genome of lung cancer
Mutational Analysis of Quinolone Resistance Protein QnrB1
Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia
Mutations in FKBP10 Cause Both Bruck Syndrome and Isolated Osteogenesis Imperfecta in Humans
Mutations Seen Among Patients with Pheochromocytoma and Paraganglioma at a Referral Center From India
Mutation screening of RAD51C in male breast cancer patients
Mutation of Drosophila Lsd1 disrupts H3-K4 methylation, resulting in tissue-specific defects during development
Mutational analyses of the ATP6V1B1 and ATP6V0A4 genes in patients with primary distal renal tubular acidosis
Mutation-specific therapy in cystic fibrosis: the earlier, the better
Mutations in the PCNA-binding site of CDKN1C inhibit cell proliferation by impairing the entry into S phase
Mutations in PIK3CD Can Cause Hyper IgM Syndrome (HIGM) Associated with Increased Cancer Susceptibility
Mutation in hotfoot-4J mice results in retention of delta 2 glutamate receptors in ER
Mutation of the Inducible ARABIDOPSIS THALIANA CYTOCHROME P450 REDUCTASE2 Alters Lignin Composition and Improves Saccharification
Mutational spaces for leaf shape and size
Mutational Analysis of Oculocutaneous Albinism: A Compact Review
Mutations of ETNK1 in aCML and CMML
Mutational Analyses of Glucose Dehydrogenase and Glucose-6-Phosphate Dehydrogenase Genes in Pseudomonas fluorescens Reveal Their Effects on Growth and Alginate Production
Mutation specific functions of EGFR result in a mutation-specific downstream pathway activation
Mutation-Specific RAS Oncogenicity Explains NRAS Codon 61 Selection in Melanoma
Mutations in JAGGED1 gene are predominantly sporadic in alagille syndrome
Mutation in katG315 is, possibly, a good prognostic marker for treatment with second-line drugs in multi-drug resistant tuberculosis: A preliminary study
Mutations in HPCA Cause Autosomal-Recessive Primary Isolated Dystonia
Mutation in pre-mRNA adenosine deaminase markedly attenuates neuronal tolerance to O-2 deprivation in Drosophila melanogaster (vol 107, pg 685, 2001)
Mutational analysis of the internal membrane proximal domain of the HIV glycoprotein C-terminus
Mutation in ADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus
Mutations that delay flowering in Arabidopsis de-couple symptom response from cauliflower mosaic virus accumulation during infection
Mutagenesis by asbestos in the lung of lambda-lacI transgenic rats
Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal-Recessive Cone-Rod Dystrophy and Amelogenesis Imperfecta
Mutant p53 exerts oncogenic effects through microRNAs and their target gene networks
Mutant p53 Cooperates with Knockdown of Endogenous Wild-Type p53 to Disrupt Tubulogenesis in Madin-Darby Canine Kidney Cells
Mutation mapping of apolipoprotein A-I structure assisted with the putative cholesterol recognition regions
Mutant Huntingtin promotes autonomous microglia activation via myeloid lineage-determining factors
Mutations in the tricarboxylic acid cycle enzyme, aconitase 2, cause either isolated or syndromic optic neuropathy with encephalopathy and cerebellar atrophy
Mutant glucocerebrosidase in Gaucher disease recruits Hsp27 to the Hsp90 chaperone complex for proteasomal degradation
Mutations of the HIPK2 gene in acute myeloid leukemia and myelodysplastic syndrome impair AML1-and p53-mediated transcription
Mutation of SCARB2 in a Patient With Progressive Myoclonus Epilepsy and Demyelinating Peripheral Neuropathy
Mutations in KRT5 and KRT14 cause epidermolysis bullosa simplex in 75% of the patients
Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study
Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13)
Mutations in HIV-1 gag and pol Compensate for the Loss of Viral Fitness Caused by a Highly Mutated Protease
Mutations and Polymorphisms in the Proprotein Convertase Subtilisin Kexin 9 (PCSK9) Gene in Cholesterol Metabolism and Disease
Mutational Uncoupling of the Role of Sus1 in Nuclear Pore Complex Targeting of an mRNA Export Complex and Histone H2B Deubiquitination
Mutations in oncogenes: Context matters
Mutations in IAPP and NEUROG3 genes are not a common cause of permanent neonatal/infancy/childhood-onset diabetes
Mutational analysis of TOX3 in Chinese Han women with polycystic ovary syndrome
Mutational and crystallographic analysis of L-amino acid oxidase/monooxygenase from Pseudomonas sp AIU 813: Interconversion between oxidase and monooxygenase activities
Mutational inactivation of two distinct negative RNA elements in the human papillomavirus type 16 L2 coding region induces production of high levels of L2 in human cells
Mutations in the BC-Loop of the BKV VP1 Region Do Not Influence Viral Load in Renal Transplant Patients
Mutatis Mutandis: Harmonize the Standard!
Mutational profiling of the variability of individual amino acid positions in the hepatitis B virus matrix domain
Mutant strains of Pichia pastoris with enhanced secretion of recombinant proteins
Mutations at positions 547-553 of rat glucocorticoid receptors reveal that hsp90 binding requires the presence, but not defined composition, of a seven-amino acid sequence at the amino terminus of the ligand binding domain
Mutation in the LPS outer core biosynthesis gene, galU, affects LPS interaction with the RTX toxins ApxI and ApxII and cytolytic activity of Actinobacillus pleuropneumoniae serotype 1
Mutations in NPC1L1 and Coronary Heart Disease
Mutation Profiling and Microsatellite Instability in Stage II and III Colon Cancer: An Assessment of Their Prognostic and Oxaliplatin Predictive Value
Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions (vol 57, pg 338, 2012)
Mutant TP53 in Duodenal Samples of Pancreatic Juice From Patients With Pancreatic Cancer or High-Grade Dysplasia
Mutation of the PIK3CA gene in anaplastic thyroid cancer
Mutation of Threonine 34 in Mouse Podoplanin-Fc Reduces CLEC-2 Binding and Toxicity in Vivo While Retaining Anti-lymphangiogenic Activity
Mutations in U4atac snRNA, a Component of the Minor Spliceosome, in the Developmental Disorder MOPD I
Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome
Mutations in COA6 cause Cytochrome c Oxidase Deficiency and Neonatal Hypertrophic Cardiomyopathy
Mutational analysis of predicted extracellular domains of human growth hormone secretagogue receptor 1a
Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome
Mutational and selective effects on copy-number variants in the human genome
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F
Mutational analysis of PMP22, GJB1 and MPZ in Greek Charcot-Marie-Tooth type 1 neuropathy patients
Mutations at cleave gag sites and the change of reading frame gag-pol HIV-1 and virological response to treatment with protasis inhibitors
Mutagen Sensitivity in Oral Cancer Patients, Healthy Tobacco Chewers and Controls
Mutations in TPM2 and congenital fibre type disproportion
Mutational analysis of Kir6.1 in Japanese patients with coronary spastic angina
Mutational analysis of the ACVR1 gene in Italian patients affected with fibrodysplasia ossificans progressiva: confirmations and advancements
Mutational screening of ACVR1 gene in Brazilian fibrodysplasia ossificans progressiva patients
Mutagenic effects of 4-hydroxynonenal triacetate, a chemically protected form of the lipid peroxidation product 4-hydroxynonenal, as assayed in L5178Y/Tk(+/-) mouse lymphoma cells
Mutant superoxide dismutase 1 (SOD1), a cause of amyotrophic lateral sclerosis, disrupts the recruitment of SMN, the spinal muscular atrophy protein to nuclear Cajal bodies
Mutation and Selection of Prions
Mutation Scanning in a Single and a Stacked Genetically Modified (GM) Event by Real-Time PCR and High Resolution Melting (HRM) Analysis
Mutable elastic models for sculpting structured shapes
Mutations in Glucose Transporter 9 Gene SLC2A9 Cause Renal Hypouricemia
Mutator alleles of yeast DNA polymerase zeta
Mutations in clusters and showers
Mutation as a stress response and the regulation of evolvability
Mutability and Importance of a Hypermutable Cell Subpopulation that Produces Stress-Induced Mutants in Escherichia coli
Mutational clusters generated by non-processive polymerases: A case study using DNA polymerase beta in vitro
Mutations in the pah gene: a tool for population genetics study
Mutations within helix I of twist1 result in distinct limb defects and variation of DNA binding affinities
Mutational analysis of TP53, PTEN, PIK3CA and CTNNB1/beta-catenin genes in human herpesvirus 8-associated primary effusion lymphoma
Mutant p53 gains new function in promoting inflammatory signals by repression of the secreted interleukin-1 receptor antagonist
Mutation Analysis of the CFTR Gene in 225 Children: Identification of Five Novel Severe and Seven Reported Severe Mutations
Mutations and deletions of the SUZ12 polycomb gene in myeloproliferative neoplasms
Mutation analysis of HIF prolyl hydroxylases (PHD/EGLN) in individuals with features of phaeochromocytoma and renal cell carcinoma susceptibility
Mutational analysis of the complement receptor type 2 (CR2/CD21)-C3d interaction reveals a putative charged SCR1 binding site for C3d
Mutations in the Beta Propeller WDR72 Cause Autosomal-Recessive Hypomaturation Amelogenesis Imperfecta
Mutations in the S4 domain of a pacemaker channel alter its voltage dependence
Mutations in BCKD-kinase Lead to a Potentially Treatable Form of Autism with Epilepsy
Mutation in the SLC9A6 gene is not a frequent cause of sporadic Angelman-like syndrome
Mutant PIK3CA-bearing colon cancer cells display increased metastasis in an orthotopic model
Mutation Screen of LOXL1 in Patients With Female Pelvic Organ Prolapse
Mutation screening of the sodium iodide symporter gene in a cohort of 105 China patients with congenital hypothyroidism
Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus
Mutations in TMEM230 are not a common cause of Parkinson's disease
Mutational Status of NRAS and BRAF Genes and Protein Expression Analysis in a Series of Primary Oral Mucosal Melanoma
Mutation in the S Gene a Determinant of the Hepatitis B Virus Associated With Concomitant HBsAg and Anti-HBs in a Population in Northeastern Brazil
Mutations of RUNX1 in families with inherited thrombocytopenia
Mutational signature analysis identifies MUTYH deficiency in colorectal cancers and adrenocortical carcinomas
Mutant alpha-Synuclein Overexpression Induces Stressless Pacemaking in Vagal Motoneurons at Risk in Parkinson's Disease
Mutations in EBF3 Disturb Transcriptional Profiles and Cause Intellectual Disability, Ataxia, and Facial Dysmorphism
Mutagenic potential assessment associated-with human exposure to natural radioactivity
Mutations in INPPSK, Encoding a Phosphoinositide 5-Phosphatase, Cause Congenital Muscular Dystrophy with Cataracts and Mild Cognitive Impairment
Mutational Profile of Homozygous -Thalassemia in Rio de Janeiro, Brazil
Mutation Screening of the CHCHD10 Gene in Chinese Patients with Amyotrophic Lateral Sclerosis
Mutations in GABRB3 From febrile seizures to epileptic encephalopathies
Mutations Associated with Decreased Susceptibility to Seven Antimicrobial Families in Field and Laboratory-Derived Mycoplasma bovis Strains
Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability
Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian Families
Mutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndrome
Mutation pairs and quotient categories of Abelian categories
Mutational analysis of Kex2 recognition sites and a disulfide bond in tannase from Aspergillus oryzae
Mutation in cpsf6/CFIm68 (Cleavage and Polyadenylation Specificity Factor Subunit 6) causes short 3 ' UTRs and disturbs gene expression in developing embryos, as revealed by an analysis of primordial germ cell migration using the medaka mutant naruto
Mutations in catalase-peroxidase KatG from isoniazid resistant Mycobacterium tuberculosis clinical isolates: insights from molecular dynamics simulations
Mutant RoPI-1 allele-based marker development for selection of the hose-in-hose flower phenotype in Rhododendron obtusum cultivars
Mutation analysis of IL36RN gene in Japanese patients with palmoplantar pustulosis
Mutations in EXTL3 Cause Neuro-immuno-skeletal Dysplasia Syndrome
Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance
Mutations in the phosphatidylinositol glycan C (PIGC) gene are associated with epilepsy and intellectual disability
Mutations in the Chromatin Regulator Gene BRPF1 Cause Syndromic Intellectual Disability and Deficient Histone Acetylation
Mutational Analysis of Atypical Chemokine Receptor 3 (ACKR3/CXCR7) Interaction with Its Chemokine Ligands CXCL11 and CXCL12
Mutations and interactions in human ER alpha and bZIP proteins: An in silico approach for cell signaling in breast oncology
Mutation Pattern in the Genome of Neisseria gonorrhoeae and Its Association with Multidrug-resistant Isolates from Delhi, India
Mutation Analysis in Classical Phenylketonuria Patients Followed by Detecting Haplotypes Linked to Some PAH Mutations
Mutation analysis of connexin 50 gene among Iranian families with autosomal dominant cataracts
Mutation analysis of sporadic early-onset Alzheimer's disease using the NeuroX array
Mutations in sphingosine-1-phosphate lyase cause nephrosis with ichthyosis and adrenal insufficiency
Mutations in POGLUT1 in Galli-Galli/Dowling-Degos disease
Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening
Mutagenic products are promoted in the nitrosation of tyramine
Mutation of the Ser18 phosphorylation site on the sole Saccharomyces cerevisiae UCS protein, She4, can compromise high-temperature survival
Mutantelec: An In Silico Mutation Simulation Platform for Comparative Electrostatic Potential Profiling of Proteins
Mutant KRAS promotes malignant pleural effusion formation
Mutational Analysis of Mitochondrial tRNA Genes in Patients with Asthma
Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjogren Syndrome and Dystroglycanopathy
Mutant KRAS Status Is Associated with Increased KRAS Copy Number Imbalance: a Potential Mechanism of Molecular Heterogeneity
Mutation analysis of TRPS1 gene including core promoter, 5 ' UTR, and 3 ' UTR regulatory sequences with insight into their organization
Mutations at the Q(o) Site of the Cytochrome bc(1) Complex Strongly Affect Oxygen Binding
Mutations in chromatin regulators functionally link Cornelia de Lange syndrome and clinically overlapping phenotypes
Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome
Mutations in MDH2, Encoding a Krebs Cycle Enzyme, Cause Early-Onset Severe Encephalopathy
Mutation in clpC1 encoding an ATP-dependent ATPase involved in protein degradation is associated with pyrazinamide resistance in Mycobacterium tuberculosis
Mutation effects predicted from sequence co-variation
Mutations at the Darkener of Apricot locus modulate pheromone production and sex behavior in Drosophila melanogaster
Mutation in the L3 Ribosomal Protein Could Be Associated with Risk of Selection of High-Level Linezolid-Resistant Staphylococcus epidermidis Strains
Mutations in the leukemia inhibitory factor receptor (LIFR) gene and Lifr deficiency cause urinary tract malformations
Mutation of the Human Circadian Clock Gene CRY1 in Familial Delayed Sleep Phase Disorder
Mutant IDH1 Disrupts the Mouse Subventricular Zone and Alters Brain Tumor Progression
Mutations in Cas9 Enhance the Rate of Acquisition of Viral Spacer Sequences during the CRISPR-Cas Immune Response
Mutational analysis of HOXA10 gene in Chinese patients with cryptorchidism
Mutational Landscape and Gene Expression Patterns in Adult Acute Myeloid Leukemias with Monosomy 7 as a Sole Abnormality
Mutation matters in precision medicine: A future to believe in
Mutagenic Replication of N-2-Deoxyguanosine Benzo[a]pyrene Adducts by Escherichia coli DNA Polymerase I and Sulfolobus solfataricus DNA Polymerase IV
Mutation Analysis of Cell-Free DNA and Single Circulating Tumor Cells in Metastatic Breast Cancer Patients with High Circulating Tumor Cell Counts
Mutations in BOREALIN cause thyroid dysgenesis
Mutation Location on the RAS Oncogene Affects Pathologic Features and Survival After Resection of Colorectal Liver Metastases
Mutated Chromatin Regulatory Factors as Tumor Drivers in Cancer
Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndrome of Orofacial Clefting and Cor Triatriatum Sinister in Humans and Mice
Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia
Mutation Detection of Fibroblast Growth Factor Receptor 3 for Infiltrative Hepatocellular Carcinoma by Whole-Exome Sequencing
Mutation operators for testing Android apps
Mutation of Kinesin-6 Kif20b causes defects in cortical neuron polarization and morphogenesis
Mutation in sorghum LOW GERMINATION STIMULANT 1 alters strigolactones and causes Striga resistance
Mutant p53 establishes targetable tumor dependency by promoting unscheduled replication
Mutant IDH1 regulates the tumor-associated immune system in gliomas
Mutational spectra of aflatoxin B1 in vivo establish biomarkers of exposure for human hepatocellular carcinoma
Mutating the CX3C Motif in the G Protein Should Make a Live Respiratory Syncytial Virus Vaccine Safer and More Effective
Mutations of PQBP1 in Renpenning syndrome promote ubiquitin-mediated degradation of FMRP and cause synaptic dysfunction
Mutant p53 Together with TGF beta Signaling Influence Organ-Specific Hematogenous Colonization Patterns of Pancreatic Cancer
Mutations along a TET2 active site scaffold stall oxidation at 5-hydroxymethylcytosine
Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism
Mutations underlying Episodic Ataxia type-1 antagonize Kv1.1 RNA editing
Mutant p53 Gain of Function and Chemoresistance: The Role of Mutant p53 in Response to Clinical Chemotherapy
Mutational Analysis of the QRRQ Motif in the Yeast Hig1 Type 2 Protein Rcf1 Reveals a Regulatory Role for the Cytochrome c Oxidase Complex
Mutagen resistance and mutation restriction of St. Louis encephalitis virus
Mutation profiles in early-stage lung squamous cell carcinoma with clinical follow-up and correlation with markers of immune function
Mutants in the imprinted PICKLE RELATED 2 gene suppress seed abortion of fertilization independent seed class mutants and paternal excess interploidy crosses in Arabidopsis
Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopenia
Mutational landscape of mucinous ovarian carcinoma and its neoplastic precursors (vol 7, 87, 2015)
Mutations and reduced expression of p53 gene are involved in HPV-independent oncogenesis of cervical cancer
Mutant p53 perturbs DNA replication checkpoint control through TopBP1 and Treslin
Mutational analysis to identify the residues essential for the acetyltransferase activity of GlmU in Bacillus subtilis
Mutation of the caspase-3 cleavage site in the astroglial glutamate transporter EAAT2 delays disease progression and extends lifespan in the SOD1-G93A mouse model of ALS
Mutagenicity and oxidative damage induced by an organic extract of the particulate emissions from a simulation of the deepwater horizon surface oil burns
Mutational Markers and Risk Stratification in Thyroid Cancer-The Art of War Refined
Mutant RAS Calms Stressed-Out Cancer Cells
Mutation Accumulation in an Asexual Relative of Arabidopsis
Mutant Profilin1 transgenic mice recapitulate cardinal features of motor neuron disease
Mutational studies on single circulating tumor cells isolated from the blood of inflammatory breast cancer patients
Mutant IDH1 and seizures in patients with glioma
Mutation-Induced Functional Alterations of CCR6
Mutations in Argonaute5 Illuminate Epistatic Interactions of the K1 and / Loci Leading to Saddle Seed Color Patterns in Glycine max
Mutations of two acidic residues at the cytoplasmic end of segment IIIS6 of an insect sodium channel have distinct effects on pyrethroid resistance
Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis
Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability
Mutations in mitochondrial DNA causing tubulointerstitial kidney disease
Mutations in the Non-Catalytic Subunit Dpb2 of DNA Polymerase Epsilon Affect the Nrm1 Branch of the DNA Replication Checkpoint
Mutational analysis of the RNA helicase Dhh1 in Ste12 expression and yeast mating
Mutational analysis of protein folding inside the ribosome exit tunnel
Mutations in COL1A1 and COL1A2 and dental aberrations in children and adolescents with osteogenesis imperfecta - A retrospective cohort study
Mutation Supply and Relative Fitness Shape the Genotypes of Ciprofloxacin-Resistant Escherichia coli
Mutations of the aminoacyl-tRNA-synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disability
Mutant CCL2 protein coating mitigates wear particle-induced bone loss in a murine continuous polyethylene infusion model
Mutagenesis Analysis Reveals Distinct Amino Acids of the Human Serotonin 5-HT2c Receptor Underlying the Pharmacology of Distinct Ligands
Mutant Huntingtin Disrupts the Nuclear Pore Complex
Mutational analysis of hypermutation-related POLE gene in acute leukemias and lymphomas
Mutational spectrum of the SERPING1 gene in Swiss patients with hereditary angioedema
Mutational analysis of the GLA gene in Mexican families with Fabry disease
Mutagenicity assessment of aerosols in emissions from domestic combustion processes
Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
Mutagenicity of a Model DNA-Peptide Cross-Link in Human Cells: Roles of Translesion Synthesis DNA Polymerases
Mutants for Drosophila Isocitrate Dehydrogenase 3b Are Defective in Mitochondrial Function and Larval Cell Death
Mutational landscape send response are conserved in peripheral blood of aml and mds patients during deciabine therapy
Mutations and mechanisms in congenital and age-related cataracts
Mutations induce conformational changes in folliculin C-terminal domain: possible cause of loss of guanine exchange factor activity and Birt-Hogg-Dube syndrome
Mutations in gamma-secretase subunit-encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
Mutations near the cleavage site of enterocin NKR-5-3B prepeptide reveal new insights into its biosynthesis
Mutant U2AF1-expressing cells are sensitive to pharmacological modulation of the spliceosome
Mutant p53: a novel target for the treatment of patients with triple-negative breast cancer?
Mutation Profile and Fluorescence In Situ Hybridization Analyses Increase Detection of Malignancies in Biliary Strictures
Mutagenic activities of biochars from pyrolysis
Mutational Analysis at Intersubunit Interfaces of an Anionic Glutamate Receptor Reveals a Key Interaction Important for Channel Gating by Ivermectin
Mutant reduction based on dominance relation for weak mutation testing
Mutant allele specific imbalance in oncogenes with copy number alterations: Occurrence, mechanisms, and potential clinical implications
Mutant eIF2B leads to impaired mitochondrial oxidative phosphorylation in vanishing white matter disease
Mutations in the NEB gene cause fetal akinesia/arthrogryposis multiplex congenita
Mutational Signatures in Breast Cancer: The Problem at the DNA Level
Mutations in MAPKBP1 Cause Juvenile or Late-Onset Cilia-Independent Nephronophthisis
Mutations in linker for activation of T cells (LAT) lead to a novel form of severe combined immunodeficiency
Mutations in TMEM260 Cause a Pediatric Neurodevelopmental, Cardiac, and Renal Syndrome
Mutations affecting the transmembrane domain of the LDL receptor: impact of charged residues on the membrane insertion
Mutational profiling of acute lymphoblastic leukemia with testicular relapse
Mutational Landscape of Pediatric Acute Lymphoblastic Leukemia
Mutant TDP-43 within motor neurons drives disease onset but not progression in amyotrophic lateral sclerosis
Mutational profiling of a MonoMAC syndrome family with GATA2 deficiency
Mutant A53T alpha-Synuclein Improves Rotarod Performance Before Motor Deficits and Affects Metabolic Pathways
Mutations that Allow SIR2 Orthologs to Function in a NAD(+)-Depleted Environment
Mutant Ataxin-1 Inhibits Neural Progenitor Cell Proliferation in SCA1
Mutations in C19orf12 and intronic repeat expansions in C9orf72 not observed in Iranian Parkinson's disease patients
Mutations in TRAPPC11 are associated with a congenital disorder of glycosylation
Mutational spectrum of CENP-B box and alpha-satellite DNA on chromosome 21 in Down syndrome children
Mutations in the maize zeta-carotene desaturase gene lead to viviparous kernel
Mutation of AREA affects growth, sporulation, nitrogen regulation, and pathogenicity in Colletotrichum gloeosporioides
Mutation in Mg-Protoporphyrin IX Monomethyl Ester Cyclase Decreases Photosynthesis Capacity in Rice
Mutation of miR-21 targets endogenous lipoprotein receptor-related protein 6 and nonalcoholic fatty liver disease
Mutation of neuron-specific chromatin remodeling subunit BAF53b: rescue of plasticity and memory by manipulating actin remodeling
Mutation screening of PDGFB gene in Chinese population with primary familial brain calcification
Mutation of the N-Terminal Region of Chikungunya Virus Capsid Protein: Implications for Vaccine Design
Mutations of the LIM protein AJUBA mediate sensitivity of head and neck squamous cell carcinoma to treatment with cell-cycle inhibitors
Mutation screening of the LRIT3, CABP4, and GPR179 genes in Chinese patients with Schubert-Bornschein congenital stationary night blindness
Mutational analysis of GSC, HOXA2 and PRKRA in 106 Chinese patients with microtia
Mutations in apoptotic genes and micronucleus occurrence in vinyl chloride-exposed workers in China
Mutations of the Transporter Proteins GlpT and UhpT Confer Fosfomycin Resistance in Staphylococcus aureus
Mutant presenilin2 promotes apoptosis through the p53/miR-34a axis in neuronal cells
Mutation screening of the PRRT2 gene for benign epilepsy with centrotemporal spikes in Chinese mainland population
Mutations of CCNF gene is rare in patients with amyotrophic lateral sclerosis and frontotemporal dementia from Mainland China
Mutation of Tyr137 of the universal Escherichia coli fimbrial adhesin FimH relaxes the tyrosine gate prior to mannose binding
Mutant DD genotype of NFKB1 gene is associated with the susceptibility and severity of coronary artery disease
Mutational screening of SLC39A5, LEPREL1 and LRPAP1 in a cohort of 187 high myopia patients
Mutations of cancer-related genes in benign tumors: the example of hidradenoma papilliferum
Mutation Analysis of HTRA2 Gene in Chinese Familial Essential Tremor and Familial Parkinson's Disease
Mutational landscape reflects the biological continuum of plasma cell dyscrasias
Mutation spectrum of NF1 gene in Italian patients with neurofibromatosis type 1 using Ion Torrent PGM (TM) platform
Mutational analysis and overproduction effects of MotX, an essential component for motor function of Na+-driven polar flagella of Vibrio
Mutations Inactivating Herpes Simplex Virus 1 MicroRNA miR-H2 Do Not Detectably Increase ICP0 Gene Expression in Infected Cultured Cells or Mouse Trigeminal Ganglia
Mutation in VPS33A affects metabolism of glycosaminoglycans: a new type of mucopolysaccharidosis with severe systemic symptoms
Mutation Profile of B-Raf Gene Analyzed by fully Automated System and Clinical Features in Japanese Melanoma Patients
Mutational randomness as conditional independence and the experimental vindication of mutational Lamarckism
Mutacins and bacteriocins like genes in Streptococcus mutans isolated from participants with high, moderate, and low salivary count
Mutational landscape of combined hepatocellular carcinoma and cholangiocarcinoma, and its clinicopathological significance
Mutant KIT as imatinib-sensitive target in metastatic sinonasal carcinoma
Mutagenic Factors and Complex Clonal Relationship of Multifocal Urothelial Cell Carcinoma
Mutational spectrum of Chinese LGMD patients by targeted next-generation sequencing
Mutation Analysis of FGFR1-3 in 11 Japanese Patients with Syndromic Craniosynostoses
Mutation analysis for the detection of long QT-syndrome (LQTS) associated SNPs
Mutation Spectrum of the ABCA4 Gene in 335 Stargardt Disease Patients From a Multicenter German Cohort-Impact of Selected Deep Intronic Variants and Common SNPs
Mutated olfactomedin 1 in the interphotoreceptor matrix of the mouse retina causes functional deficits and vulnerability to light damage
Mutation analysis of tumor necrosis factor alpha-induced protein 3 gene in Hodgkin lymphoma
Mutant alpha 2-chimaerin signals via bidirectional ephrin pathways in Duane retraction syndrome
Mutagenic Azo Dyes, Rather Than Flame Retardants, Are the Predominant Brominated Compounds in House Dust
Mutation of the Second Sialic Acid-Binding Site, Resulting in Reduced Neuraminidase Activity, Preceded the Emergence of H7N9 Influenza A Virus
Mutations in PIH1 D3 Cause X-Linked Primary Ciliary Dyskinesia with Outer and Inner Dynein Arm Defects
Mutational Analysis of Recurrent Meningioma Progressing From Atypical to Rhabdoid Subtype
Mutation of representations and nearly Morita equivalence
Mutations acquired by hepatocellular carcinoma recurrence give rise to an aggressive phenotype
Mutation patterns in small cell and non-small cell lung cancer patients suggest a different level of heterogeneity between primary and metastatic tumors
Mutagenesis of nisin's leader peptide proline strongly modulates export of precursor nisin
Mutations in PMR1 stimulate xylose isomerase activity and anaerobic growth on xylose of engineered Saccharomyces cerevisiae by influencing manganese homeostasis
Mutagenicity and cytotoxicity evaluation of photo-catalytically treated petroleum refinery wastewater using an array of bioassays
Mutations in IL36RN are associated with geographic tongue
Mutational screening of GLI3, SHH, preZRS, and ZRS in 102 Chinese children with nonsyndromic polydactyly
Mutations in methionyl-tRNA synthetase gene in a Chinese family with interstitial lung and liver disease, postnatal growth failure and anemia
Mutation Screening of Gata4 Gene in CTD Patients Within Chinese Han Population
Mutations in valosin-containing protein (VCP) decrease ADP/ATP translocation across the mitochondrial membrane and impair energy metabolism in human neurons
Mutations and mechanism: how PINK1 may contribute to risk of sporadic Parkinson's disease
Mutations in SLC25A22: hyperprolinaemia, vacuolated fibroblasts and presentation with developmental delay
Mutations in noncoding regions of GJB1 are a major cause of X-linked CMT
Mutation of a kinase allosteric node uncouples dynamics linked to phosphotransfer
Mutations in AAGAB underlie autosomal dominant punctate palmoplantar keratoderma
Mutant TDP-43 does not impair mitochondrial bioenergetics in vitro and in vivo
Mutations in SLC5A6 associated with brain, immune, bone, and intestinal dysfunction in a young child
Mutations of EXOSC3/Rrp40p associated with neurological diseases impact ribosomal RNA processing functions of the exosome in S-cerevisiae
Mutation G1629E Increases von Willebrand Factor Cleavage via a Cooperative Destabilization Mechanism
Mutation of MED12 is not a frequent occurrence in, prostate cancer of Korean patients
Mutations of CREBBP and SOCS1 are independent prognostic factors in diffuse large B cell lymphoma: mutational analysis of the SAKK 38/ 07 prospective clinical trial cohort
Mutational landscape in children with myelodysplastic syndromes is distinct from adults: specific somatic drivers and novel germline variants
Mutational screening in genes related with porto-pulmonary hypertension: An analysis of 6 cases
Mutations in DNA Gyrase and Topoisomerase IV in Ciprofloxacin-Nonsusceptible Extended-Spectrum beta-Lactamase-Producing Escherichia coli and Klebsiella pneumoniae: a Statistical Analysis
Mutations in Durum Wheat SBEII Genes affect Grain Yield Components, Quality, and Fermentation Responses in Rats
Mutations in FA2H in three Arab families with a clinical spectrum of neurodegeneration and hereditary spastic paraparesis
Mutation of EpCAM leads to intestinal barrier and ion transport dysfunction
Mutational Profiling Can Establish Clonal or Independent Origin in Synchronous Bilateral Breast and Other Tumors
Mutagenesis of the Aquaporin 4 Extracellular Domains Defines Restricted Binding Patterns of Pathogenic Neuromyelitis Optica IgG
Mutations Decouple Proton Transfer from Phosphate Cleavage in the dUTPase Catalytic Reaction
Mutation of arginine residues to avoid non-specific cellular uptakes for hepatitis B virus core particles
Mutations in histone modulators are associated with prolonged survival during azacitidine therapy
Mutation Analysis of Nine Chordoma Specimens by Targeted Next-Generation Cancer Panel Sequencing
Mutant Huntingtin Does Not Affect the Intrinsic Phenotype of Human Huntington's Disease T Lymphocytes
Mutations and long-term outcome of 217 young patients with essential thrombocythemia or early primary myelofibrosis
Mutant p53 stimulates chemoresistance of pancreatic adenocarcinoma cells to gemcitabine
Mutations conferring resistance to first- and second-line drugs in multidrug-resistant Mycobacterium tuberculosis clinical isolates in southeast Mexico
Mutation at embB Codon 306, a Potential Marker for the Identification of Multidrug Resistance Associated with Ethambutol in Mycobacterium tuberculosis
Mutations of Glucose-6-Phosphate Dehydrogenase Durham, Santa-Maria and A plus Variants Are Associated with Loss Functional and Structural Stability of the Protein
Mutations in an antisense RNA, involved in the replication control of a repABC plasmid, that disrupt plasmid incompatibility and mediate plasmid speciation
Mutations in the noncoding genome
Mutations in hereditary phosphoglucomutase 1 deficiency map to key regions of enzyme structure and function
Mutations that Separate the Functions of the Proofreading Subunit of the Escherichia coli Replicase
Mutations in the 5 ' NTR and the Non-Structural Protein 3A of the Coxsackievirus B3 Selectively Attenuate Myocarditogenicity
Mutagenic effects induced by the attack of NO2 radical to the guanine-cytosine base pair
Mutational Analysis of Rab3 Function for Controlling Active Zone Protein Composition at the Drosophila Neuromuscular Junction
Mutational analysis of PKD1 gene in a Chinese family with autosomal dominant polycystic kidney disease
Mutational Analyses of the FMR1 Gene in Chinese Pediatric Population of Fragile X Suspects: Low Tolerance for Point Mutation
Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China
Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress and increased mitochondrial Ca2+
Mutated MCM9 is associated with predisposition to hereditary mixed polyposis and colorectal cancer in addition to primary ovarian failure
Mutations of c-Cbl in myeloid malignancies
Mutation-The Engine of Evolution: Studying Mutation and Its Role in the Evolution of Bacteria
Mutations within the spliceosomal gene SNRPB affect its auto-regulation and are causative for classic cerebro-costo-mandibular syndrome
Mutation of histone H-3 serine 86 disrupts GATA factor Ams2 expression and precise chromosome segregation in fission yeast
Mutation analysis underlying the downregulation of the thyroid hormone receptor beta 1 gene in the Chinese breast cancer population
Mutations in the DI-DII Linker of Human Parainfluenza Virus Type 3 Fusion Protein Result in Diminished Fusion Activity
Mutations in the Leucine Zipper-Like Motif of the Human Parainfluenza Virus 3 Fusion Protein Impair Fusion Activity
Mutation analyses and prenatal diagnosis in families of X-linked severe combined immunodeficiency caused by IL2R gamma gene novel mutation
Mutation of the epidermal growth factor receptor gene and its impact on the efficacy of gefitinib in advanced non-small cell lung cance
Mutations of desmoglein-2 in sudden death from arrhythmogenic right ventricular cardiomyopathy and sudden unexplained death
Mutational landscape and complexity in CLL
Mutation in BMPR2 Promoter: A 'Second Hit' for Manifestation of Pulmonary Arterial Hypertension?
Mutational analysis of BRCA1/2 gene and pathologic characteristics from Kazakh population with sporadic breast cancer in northwestern China
Mutants of Micromonospora viridifaciens sialidase have highly variable activities on natural and non-natural substrates
Mutations in the BCR-ABL1 Kinase Domain and Elsewhere in Chronic Myeloid Leukemia
Mutational profiling of colorectal cancers with microsatellite instability
Mutational analysis of SYNJ1 gene (PARK20) in Parkinson's disease in a Taiwanese population
Mutation genotypes of RNF213 gene from moyamoya patients in Taiwan
Mutations in LRRK2 potentiate age-related impairment of autophagic flux
Mutation profiling for detection of isoniazid resistance in Mycobacterium tuberculosis clinical isolates
Mutation analysis of 6 spinocerebellar ataxia (SCA) types in patients from southern Turkey
Mutation analysis of CACNA1S and SCN4A in patients with hypokalemic periodic paralysis
Mutant prevention concentrations of levofloxacin, pazufloxacin and ciprofloxacin for A. baumannii and mutations in gyrA and parC genes
Mutations in the Kinase Domain of the HER2/ERBB2 Gene Identified in a Wide Variety of Human Cancers
Mutation analysis in patients with total sperm immotility
Mutations Affecting Keratin 10 Surface-Exposed Residues Highlight the Structural Basis of Phenotypic Variation in Epidermolytic Ichthyosis
Mutation in galP improved fermentation of mixed sugars to succinate using engineered Escherichia coli AS1600a and AM1 mineral salts medium
Mutations can cause light chains to be too stable or too unstable to form amyloid fibrils
Mutagenic Deimmunization of Diphtheria Toxin for Use in Biologic Drug Development
Mutations in CIZ1 Are Not a Major Cause for Dystonia in Germany
Mutational Spectrum Analysis of Neurodegenerative Diseases and Its Pathogenic Implication
Mutability in Pseudomonas viridiflava as a programmed balance between antibiotic resistance and pathogenicity
Mutations and sequence variants in GDF9, BMP15, and BMPR1B genes in Maremmana cattle breed with single and twin births
Mutation of a Single Envelope N-Linked Glycosylation Site Enhances the Pathogenicity of Bovine Leukemia Virus
Mutation analysis of PVRL1 in patients with non-syndromic cleft of the lip and/or palate in Guangdong
Mutation of Rv2887, a marR-Like Gene, Confers Mycobacterium tuberculosis Resistance to an Imidazopyridine-Based Agent
Mutation of Gly717Phe in human topoisomerase 1B has an effect on enzymatic function, reactivity to the camptothecin anticancer drug and on the linker domain orientation
Mutagenic Effects of Potassium Dichromate as Evaluated by Means of Animal and Plant Bioindicators
Mutational status of naevus-associated melanomas
Mutations in the plant-conserved MTERF9 alter chloroplast gene expression, development and tolerance to abiotic stress in Arabidopsis thaliana
Mutational profile of childhood myeloproliferative neoplasms
Mutagenic Effects of NanosilverConsumer Products: a new Approach to Physicochemical Properties
Mutational dichotomy in desmoplastic malignant melanoma corroborated by multigene panel analysis
Mutations of mitochondrial genome in carotid atherosclerosis
Mutations in SPECC1L, encoding sperm antigen with calponin homology and coiled-coil domains 1-like, are found in some cases of autosomal dominant Opitz G/BBB syndrome
Mutation Spectrum of RB1 Gene in Unilateral Retinoblastoma Cases from Tunisia and Correlations with Clinical Features
Mutation-biased adaptation in Andean house wrens
Mutagenicity monitoring following battlefield exposures: Longitudinal study of HPRT mutations in gulf war i veterans exposed to depleted uranium
Mutations of the functional ARH1 allele in tumors from ARH1 heterozygous mice and cells affect ARH1 catalytic activity, cell proliferation and tumorigenesis
Mutation load under additive fitness effects
Mutations in the bacterial cell division protein FtsZ highlight the role of GTP binding and longitudinal subunit interactions in assembly and function
Mutations in NalC induce MexAB-OprM overexpression resulting in high level of aztreonam resistance in environmental isolates of Pseudomonas aeruginosa
Mutational analysis of ATP7B in Chinese Wilson disease patients
Mutations for Worse or Better: Low-Fidelity DNA Synthesis by SOS DNA Polymerase V Is a Tightly Regulated Double-Edged Sword
Mutations in Novel Lipopolysaccharide Biogenesis Genes Confer Resistance to Amoebal Grazing in Synechococcus elongatus
Mutagenic and cytotoxic activities of Limonium globuliferum methanol extracts
Mutagenic and cytotoxic activities of benfuracarb insecticide
Mutations in the haemagglutinin protein and their effect in transmission of highly pathogenic avian influenza (HPAI) H5N1 virus in sub-optimally vaccinated chickens
Mutation based treatment recommendations from next generation sequencing data: a comparison of web tools
Mutation characterization and heterodimer analysis of patients with leukocyte adhesion deficiency: Including one novel mutation
Mutations on M3 helix of Plutella xylostella glutamate-gated chloride channel confer unequal resistance to abamectin by two different mechanisms
Mutations in NKX6-2 Cause Progressive Spastic Ataxia and Hypomyelination
Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease
Mutational landscape of B-cell post-transplant lymphoproliferative disorders
Mutational spectrum of EDA and EDAR genes in a cohort of Mexican mestizo patients with hypohidrotic ectodermal dysplasia
Mutations in EFL1, an SBDS partner, are associated with infantile pancytopenia, exocrine pancreatic insufficiency and skeletal anomalies in a Shwachman-Diamond like syndrome
Mutations in mitochondrial tRNA genes may be related to insulin resistance in women with polycystic ovary syndrome
Mutations in the CCND1 and CCND2 genes are frequent events in adult patients with t(8;21)(q22;q22) acute myeloid leukemia
Mutagenesis of Dengue Virus Protein NS2A Revealed a Novel Domain Responsible for Virus-Induced Cytopathic Effect and Interactions between NS2A and NS2B Transmembrane Segments
Mutation analysis and copy number changes of KRAS and BRAF genes in Taiwanese cases of biliary tract cholangiocarcinoma
Mutations of the beta-tubulin gene fragments from carbendazim-resistant isolates of Pestalotiopsis sp causing strawberry leaf blight in Chiang Mai, Thailand
Mutator转座子介导的玉米胚大小突变体的遗传分析
Mutations in Interleukin-10 Receptor and Clinical Phenotypes in Patients with Very Early Onset Inflammatory Bowel Disease: A Chinese VEO-IBD Collaboration Group Survey
Mutation in the ace-1 gene of the tomato leaf miner (Tuta absoluta) associated with organophosphates resistance
Mutation-Enrichment Next-Generation Sequencing for Quantitative Detection of KRAS Mutations in Urine Cell-Free DNA from Patients with Advanced Cancers
Mutant spastin proteins promote deficits in axonal transport through an isoform-specific mechanism involving casein kinase 2 activation
Mutations in KDSR Cause Recessive Progressive Symmetric Erythrokeratoderma
Mutagenesis and expression of methane monooxygenase to alter regioselectivity with aromatic substrates
Mutant p53 in Cancer: Accumulation, Gain-of-Function, and Therapy
Mutations in the NOT Genes or in the Translation Machinery Similarly Display Increased Resistance to Histidine Starvation
Mutation Spectrum of STAR and the Founder Effect of p.Q258*in Korean Patients with Congenital Lipoid Adrenal Hyperplasia
Mutant Mice With Calcium-Sensing Receptor Activation Have Hyperglycemia That Is Rectified by Calcilytic Therapy
Mutational Screening of PKD1 and PKD2 Genes in Iranian Population Diagnosed with Autosomal Dominant Polycystic Kidney Disease
Mutations of PKA cyclic nucleotide-binding domains reveal novel aspects of cyclic nucleotide selectivity
Mutagenesis-Independent Stabilization of Class B Flavin Monooxygenases in Operation
Mutation screening of ACKR3 and COPS8 in kidney cancer cases from the CONFIRM study
Mutant p53 dictates the oncogenic activity of c-Abl in triple-negative breast cancers
Mutation spectrum resulting in Ml3mp2 phage DNA exposed to N-nitrosoproline with UVA irradiation
Mutation in a highly conserved glycine residue in strand 5B of plasminogen activator inhibitor 1 causes polymerisation
Mutational analysis employing a phylogenetic mass tree approach in a study of the evolution of the influenza virus
Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia
Mutation site and context dependent effects of ESR1 mutation in genome-edited breast cancer cell models
Mutant p53 upregulates alpha-1 antitrypsin expression and promotes invasion in lung cancer
Mutations in BRCA2 and taxane resistance in prostate cancer
Mutations in bla(KPC-3) That Confer Ceftazidime-Avibactam Resistance Encode Novel KPC-3 Variants That Function as Extended-Spectrum beta-Lactamases
Mutation of the inhibitory ethanol site in GABA(A) rho 1 receptors promotes tolerance to ethanol-induced motor incoordination
Mutation of the XIST gene upregulates expression of X-linked genes but decreases the developmental rates of cloned male porcine embryos
Mutations in the C-terminus of HBoV NS1 affect the function of NP1
木糖醇菠菜饼干的研制
Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in Humans
Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalities
Mutation of the Planar Cell Polarity Gene VANGL1 in Adolescent Idiopathic Scoliosis
Mutation analysis of the TUBB8 gene in nine infertile women with oocyte maturation arrest
Mutation Load of Multiple Ion Channel Gene Mutations in Brugada Syndrome
Mutagenicity of particle emissions from solid fuel cookstoves: A literature review and research perspective
Mutation spectrum in the ABCC6 gene and genotype-phenotype correlations in a French cohort with pseudoxanthoma elasticum
Mutational analysis of 29 patients with autosomal-recessive woolly hair and hypotrichosis: LIPH mutations are extremely predominant in autosomal-recessive woolly hair and hypotrichosis in Japan
Mutational analysis of cutinase-like enzyme, Cut190, based on the 3D docking structure with model compounds of polyethylene terephthalate
Mutations of the Epidermal Growth Factor Receptor Gene in Triple-Negative Breast Cancer
Mutation analysis of CTNNB1 gene and the ras pathway genes KRAS, NRAS, BRAF, and PIK3CA in eyelid sebaceous carcinomas
Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish
Mutating a conserved cysteine in GPIHBP1 reduces amounts of GPIHBP1 in capillaries and abolishes LPL binding
Mutations in DYNC2H1, the cytoplasmic dynein 2, heavy chain 1 motor protein gene, cause short-rib polydactyly type I, Saldino-Noonan type
Mutations in the 3 ' untranslated region of NOTCH1 are associated with low CD20 expression levels in chronic lymphocytic leukemia
Mutant p53 potentiates the oncogenic effects of insulin by inhibiting the tumor suppressor DAB2IP
Mutations in 5-methylcytosine oxidase TET2 and RhoA cooperatively disrupt T cell homeostasis
Mutations in AXIN2 gene as a risk factor for tooth agenesis and cancer: A review
Mutational cascades in cancer
Mutation analysis of the interactions between Mycobacterium tuberculosis caseinolytic protease C1 (ClpC1) and ecumicin
Mutations in TRAPPC12 Manifest in Progressive Childhood Encephalopathy and Golgi Dysfunction
Mutational analysis in serial marrow samples during azacitidine treatment in patients with post-transplant relapse of acute myeloid leukemia or myelodysplastic syndromes
Mutations in the Transmembrane Domain and Cytoplasmic Tail of Hendra Virus Fusion Protein Disrupt Virus-Like-Particle Assembly
Mutational and Kinetic Analysis of Lesion Recognition by Escherichia coli Endonuclease VIII
Mutations and/or Overexpressions of ERG4 and ERG11 Genes in Clinical Azoles-Resistant Isolates of Candida albicans
木碳复合材料电磁屏蔽特性分析
Mutation analysis of COL4A3 and COL4A4 genes in a Chinese autosomal-dominant Alport syndrome family
Mutation of Trp-574-Leu ALS gene confers resistance of radish biotypes to iodosulfuron and imazethapyr herbicides
Mutations in TP53 and JAK2 are independent prognostic biomarkers in B-cell precursor acute lymphoblastic leukaemia
Mutation analysis of common GJB2, SCL26A4 and 12S rRNA genes among 380 deafness patients in northern China
Mutation in the S gene of hepatitis B virus and anti-HBs subtype-nonspecificity contributed to the co-existence of HBsAg and anti-HBs in patients with chronic hepatitis B virus infection
Mutational analysis of driver genes with tumor suppressive and oncogenic roles in gastric cancer
Mutations in the Caenorhabditis elegans orthologs of human genes required for mitochondrial tRNA modification cause similar electron transport chain defects but different nuclear responses
Mutant Potential Ubiquitination Sites in Dur3p Enhance the Urea and Ethyl Carbamate Reduction in a Model Rice Wine System
Mutation of serine/threonine protein kinase 36 (STK36) causes primary ciliary dyskinesia with a central pair defect
Mutagens induced chromosomal damage in Lablab purpureus (L.) Sweet var. typicus
Mutational analysis and genotype-phenotype relation in familial hypercholesterolemia: The SAFEHEART registry
Mutable polyelectrolyte tube arrays: mesoscale modeling and lateral force microscopy
Mutational phospho-mimicry reveals a regulatory role for the XRCC4 and XLF C-terminal tails in modulating DNA bridging during classical non-homologous end joining
Mutation spectrum of RB1 mutations in retinoblastoma cases from Singapore with implications for genetic management and counselling
Mutations That Alter the Bacterial Cell Envelope Increase Lipid Production
Mutational analysis of PHEX, FGF23 and CLCN5 in patients with hypophosphataemic rickets
Mutant p53 oncogenic functions in cancer stem cells are regulated by WIP through YAP/TAZ
Mutational landscape of metastatic cancer revealed from prospective clinical sequencing of 10,000 patients
Mutation of foxl2 or cyp19a1a Results in Female to Male Sex Reversal in XX Nile Tilapia
木糖葡萄球菌添加量对发酵牛肉串品质特性的影响
Mutations targeting the coagulation pathway are enriched in brain metastases
Mutation patterns in genes encoding interferon signaling and antigen presentation: A pan-cancer survey with implications for the use of immune checkpoint inhibitors
Mutation spectrum of gehes associated with steroid-resistant nephrotic syndrome in Chinese children
Mutant HSPB1 causes loss of translational repression by binding to PCBP1, an RNA binding protein with a possible role in neurodegenerative disease
Mutational Replacements at the "Glycine Hinge" of the Escherichia coli Chemoreceptor Tsr Support a Signaling Role for the C-Helix Residue
Mutation-promoting molecular networks of uncontrolled inflammation
Mutations in LRP5, FZD4, TSPAN12, NDP, ZNF408, or KIF11 Genes Account for 38.7% of Chinese Patients With Familial Exudative Vitreoretinopathy
Mutation status among patients with sinonasal mucosal melanoma and its impact on survival
Mutation of the alpha-tubulin Tuba1a leads to straighter microtubules and perturbs neuronal migration
Mutations of MAP2K1 are frequent in pediatric-type follicular lymphoma and result in ERK pathway activation
Mutations in N-acetylglucosamine (O-GlcNAc) transferase in patients with X-linked intellectual disability
木炭颗粒对水溶液中Cd~(2+)和Cr~(3+)质量浓度的影响
木糖氧化产碱菌中亚硝酸盐还原酶基因的克隆与表达
Mutant p53 promotes cell spreading and migration via ARHGAP44
木糖醇月桂酸单酯的酶法制备工艺研究
木糖利用融合子D2的制备与乙醇发酵特性
Mutation invariance of the arc index for some montesinos knots
Mutation of the TERT promoter leads to poor prognosis of patients with non-small cell lung cancer
Mutational analysis of H3F3B gene in acute leukaemias and solid tumours
Mutational status of IGHV is the most reliable prognostic marker in trisomy 12 chronic lymphocytic leukemia
Mutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features
Mutated ASXL1 and number of somatic mutations as possible indicators of progression to chronic myelomonocytic leukemia of myelodysplastic syndromes with single or multilineage dysplasia
Mutations in TGM6 induce the unfolded protein response in SCA35
Mutation-induced loss of APP function causes GABAergic depletion in recessive familial Alzheimer%26apos;s disease: analysis of Osaka mutation-knockin mice
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly
Mutation accumulation under UV radiation in Escherichia coli
Mutant selection in the self-incompatible plant radish (Raphanus sativus L. var. sativus) using two-step TILLING
Mutation status of RAD51C, PALB2 and BRIP1 in 100 Japanese familial breast cancer cases without BRCA1 and BRCA2 mutations
Mutations in the prostate specific antigen (PSA/KLK3) correlate with male infertility
Mutants of Yarrowia lipolytica NCIM 3589 grown on waste cooking oil as a biofactory for biodiesel production
Mutagenesis and immunological evaluation of group A streptococcal C5a peptidase as an antigen for vaccine development and as a carrier protein for glycoconjugate vaccine design
Mutation analysis of the NKX2.5 gene in Iranian pediatric patients with congenital hypothyroidism
Mutational analysis in BCR-ABL1 positive leukemia by deep sequencing based on nanopore MinION technology
Mutant calreticulin causes essential thrombocythemia
Mutations in the Genes for Interphotoreceptor Matrix Proteoglycans, IMPG1 and IMPG2, in Patients with Vitelliform Macular Lesions
Mutations in ACTRT1 and its enhancer RNA elements lead to aberrant activation of Hedgehog signaling in inherited and sporadic basal cell carcinomas
Mutation of a Conserved Nuclear Export Sequence in Chikungunya Virus Capsid Protein Disrupts Host Cell Nuclear Import
Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like features
Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia
Mutation predicts 40 million years of fly wing evolution
Mutations in TYROBP are not a common cause of dementia in a Turkish cohort
Mutation Frequency of Three Neurodegenerative Lysosomal Storage Diseases: From Screening to Treatment?
Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephaly
Mutation Reduction Strategies Considered Harmful
Mutagenesis of the NaChBac sodium channel discloses a functional role for a conserved S6 asparagine
Mutation of the Putative Immunosuppressive Domain of the Retroviral Envelope Glycoprotein Compromises Infectivity
Mutator genomes decay, despite sustained fitness gains, in a long-term experiment with bacteria
Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene Panel
Mutations in DNM1L, as in OPA1, result in dominant optic atrophy despite opposite effects on mitochondrial fusion and fission
Mutations causing acrodysostosis-2 facilitate activation of phosphodiesterase 4D3
Mutation in BRAF V600E: A Poor Prognostic Marker in Stage III Colon Cancers With Deficient MMR?
Mutant CTNNB1 and histological heterogeneity define metabolic subtypes of hepatoblastoma
Mutations in the netrin-1 gene cause congenital mirror movements
Mutational signatures reveal the dynamic interplay of risk factors and cellular processes during liver tumorigenesis
Mutation in the Core Structure of Desmin Intermediate Filaments Affects Myoblast Elasticity
Mutation analysis of TGFBI and KRT12 in a case of concomitant keratoconus and granular corneal dystrophy
Mutation of Arabidopsis SMC4 identifies condensin as a corepressor of pericentromeric transposons and conditionally expressed genes
Mutational Heterogeneity in APC and KRAS Arises at the Crypt Level and Leads to Polyclonality in Early Colorectal Tumorigenesis
Mutations in the beta-Subunit of the RNA Polymerase Impair the Surface-Associated Motility and Virulence of Acinetobacter baumannii
Mutational profile of rare variants in inflammasome-related genes in Behcet disease: A Next Generation Sequencing approach
Mutations in SCAPER cause autosomal recessive retinitis pigmentosa with intellectual disability
Mutation in human CLPX elevates levels of delta-aminolevulinate synthase and protoporphyrin IX to promote erythropoietic protoporphyria
Mutagenic Effectivity of Cadmium Sulphide and Copper Oxide Nanoparticles on Some Physiological and Cytological Attributes of Lathyrus sativus L.
Mutation Frequencies in Patients With Early-Onset Colorectal Cancer Reply
Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with "Corner Fractures''
Mutant-Allele Tumor Heterogeneity Scores Correlate With Risk of Metastases in Colon Cancer
Mutations to Cysteine Residues in the Trypanosoma cruzi B-Cell Superantigen Tc24 Diminish Susceptibility to IgM-Mediated Hydrolysis
Mutational analysis of the MS2 lysis protein L
Mutational analysis of a Chinese family with oculocutaneous albinism type 2
Mutagenicity and estrogenicity of raw water and drinking water in an industrialized city in the Yangtze River Delta
Mutagenesis of Met-151 and Thr-153 to alanine in Thermoanaerobacter ethanolicus secondary alcohol dehydrogenase changes substrate specificity for acetophenones
Mutations of RNA splicing factors in hematological malignancies
Mutagenic cost of ribonucleotides in bacterial DNA
Mutations and short geodesics in hyperbolic 3-manifolds
Mutations in Membrin/GOSR2 Reveal Stringent Secretory Pathway Demands of Dendritic Growth and Synaptic Integrity
Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Mutation-Based Therapy for Duchenne Muscular Dystrophy Antisense Treatment Arrives in the Clinic
Mutant Huntingtin Is Secreted via a Late Endosomal/Lysosomal Unconventional Secretory Pathway
Mutations in MYO1H cause a recessive form of central hypoventilation with autonomic dysfunction
Mutagenic potential of hypoxanthine in live human cells
Mutational analysis using Sanger and next generation sequencing in sporadic spindle cell hemangiomas: A study of 19 cases
Mutation in TDRD9 causes non-obstructive azoospermia in infertile men
Mutations in RARS cause a hypomyelination disorder akin to Pelizaeus-Merzbacher disease
Mutations and reduced expression of p53 gene are involved in HPV-independent oncogenesis of cervical cancer (vol 10, pg 4356, 2017)
Mutational analysis of the RAS/RAF/MEK/ERK signaling pathway in 260 Han Chinese patients with cervical carcinoma
Mutation rates in 21 autosomal short tandem repeat loci in a population from Goias, Brazil
Mutations in the E2 Glycoprotein and the 3 ' Untranslated Region Enhance Chikungunya Virus Virulence in Mice
Mutational re-modeling of di-aspartyl intramembrane proteases: uncoupling physiologically-relevant activities from those associated with Alzheimer's disease
Mutations associated with drug resistance and prevalence of vaccine escape mutations in patients with chronic hepatitis B infection
Mutation in flrA and mshA Genes of Vibrio cholerae Inversely Involved in vps-Independent Biofilm Driving Bacterium Toward Nutrients in Lake Water
Mutational heterogeneity in non-serous ovarian cancers
Mutagenic, recombinogenic and carcinogenic potential of thiamethoxam insecticide and formulated product in somatic cells of Drosophila melanogaster
Mutant Huntingtin Inhibits alpha B-Crystallin Expression
Mutation landscape and intra-tumor heterogeneity of two MANECs of the esophagus revealed by multi-region sequencing
Mutation analysis and prenatal diagnosis of a family with Griscelli syndrome type 2: two novel mutations in the RAB27A gene
Mutation of N-linked glycosylation in EpCAM affected cell adhesion in breast cancer cells
Mutations in S-adenosylhomocysteine hydrolase (AHCY) affect its nucleocytoplasmic distribution and capability to interact with S-adenosylhomocysteine hydrolase-like 1 protein
Mutation in the COX4I1 gene is associated with short stature, poor weight gain and increased chromosomal breaks, simulating Fanconi anemia
Mutation of genes associated with hearing loss levels in the southern Fujian area of China
Mutations in BRAF codons 594 and 596 predict good prognosis in melanoma
Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice
Mutational profiles of Brenner tumors show distinctive features uncoupling urothelial carcinomas and ovarian carcinoma with transitional cell histology
Mutations of Pre-mRNA Splicing Regulatory Elements: Are Predictions Moving Forward to Clinical Diagnostics?
Mutation of the Slt2 ortholog from Cryphonectria parasitica results in abnormal cell wall integrity and sectorization with impaired pathogenicity
Mutation analysis and copy number alterations of KIF23 in non-small-cell lung cancer exhibiting KIF23 over-expression
Mutant p53 stimulates cell invasion through an interaction with Rad21 in human ovarian cancer cells
Mutation Frequencies in Patients With Early-Onset Colorectal Cancer
Mutagenic and genotoxic effects of Anilofos with micronucleus, chromosome aberrations, sister chromatid exchanges and Ames test
Mutational spectrum of Duchenne muscular dystrophy in Spain: Study of 284 cases
Mutant Transcriptome Sequencing Provides Insights into Pod Development in Peanut (Arachis hypogaea L.)
Mutation in a novel gene SMALL AND CORDATE LEAF 1 affects leaf morphology in cucumber
Mutation of the cyclic di-GMP phosphodiesterase gene in Burkholderia lata SK875 attenuates virulence and enhances biofihn formation
Mutations in the promoter of the telomerase gene TERT contribute to tumorigenesis by a two-step mechanism
Mutational profiling of acral melanomas in Korean populations
Mutational status of TP53 defines the efficacy of Wee1 inhibitor AZD1775 in KRAS-mutant non-small cell lung cancer
Mutation of Conserved Residues Increases in Vitro Activity of the Formylglycine-Generating Enzyme
Mutations of KIF14 cause primary microcephaly by impairing cytokinesis
Mutation of WIF1: a potential novel cause of a Nail-Patella-like disorder
Mutant p53 shapes the enhancer landscape of cancer cells in response to chronic immune signaling
Mutations in DZIP1 and XYLT1 are associated with nonsyndromic early onset high myopia in the Korean population
Mutation supply and the repeatability of selection for antibiotic resistance
Mutations that impair Eyes absent tyrosine phosphatase activity in vitro reduce robustness of retinal determination gene network output in Drosophila
Mutation in an exonic splicing enhancer site causing chronic granulomatous disease
Mutations in CHEK2 and risk of gastric cancer: a case-control study
Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly
Mutations in the fusion protein heptad repeat domains of human metapneumovirus impact on the formation of syncytia
Mutagenicity of Ochratoxin A: Role for a Carbon-Linked C8-Deoxyguanosine Adduct?
Mutations in BRCA1, BRCA2 and other breast and ovarian cancer susceptibility genes in Central and South American populations
Mutations in matrix protein 1 and nucleoprotein caused human-specific defects in nuclear exportation and viral assembly of an avian influenza H7N1 virus
Mutations in the quinolone resistance determining region conferring resistance to fluoroquinolones in Mycoplasma agalactiae
Mutation status of ras genes in breast cancers with overexpressed p21Ras protein
Mutations in the Heme Exporter FLVCR1 Cause Sensory Neurodegeneration with Loss of Pain Perception
Mutating heme oxygenase-1 into a peroxidase causes a defect in bilirubin synthesis associated with microcytic anemia and severe hyperinflammation
Mutations in the N-terminal kinase-like domain of the repressor of photomorphogenesis SPA1 severely impair SPA1 function but not light responsiveness in Arabidopsis
Mutant p53 promotes tumor progression and metastasis by the endoplasmic reticulum UDPase ENTPD5
Mutations in idiopathic cytopenia of undetermined significance assist diagnostics and correlate to dysplastic changes
Mutations in C8ORF37 cause Bardet Biedl syndrome (BBS21)
Mutation in the caveolin-3 gene causes asymmetrical distal myopathy
Mutant IDH1 Expression Drives TERT Promoter Reactivation as Part of the Cellular Transformation Process
Mutational analysis and interactions of HBV preS1 with asialoglycoprotein receptor
Mutations in Encephalomyocarditis Virus 3A Protein Uncouple the Dependency of Genome Replication on Host Factors Phosphatidylinositol 4-Kinase III alpha and Oxysterol-Binding Protein
Mutational activation of BRAF confers sensitivity to transforming growth factor beta inhibitors in human cancer cells
Mutations in TBL1X Are Associated With Central Hypothyroidism
Mutation of the 3-Phosphoinositide-Dependent Protein Kinase 1 (PDK1) Substrate-Docking Site in the Developing Brain Causes Microcephaly with Abnormal Brain Morphogenesis Independently of Akt, Leading to Impaired Cognition and Disruptive Behaviors
Mutations in PROSC Disrupt Cellular Pyridoxal Phosphate Homeostasis and Cause Vitamin-B6-Dependent Epilepsy
Mutation of a common amino acid in NKX2.5 results in dilated cardiomyopathy in two large families
Mutagenesis and TILLING to Dissect Gene Function in Plants
Mutation of the toxR or mshA genes from Vibrio coralliilyticus strain OCN014 reduces infection of the coral Acropora cytherea
Mutations in DCDC2 (doublecortin domain containing protein 2) in neonatal sclerosing cholangitis
Mutation analysis of NANOS3 in Brazilian women with primary ovarian failure
Mutant TP53 disrupts age-related accumulation patterns of somatic mutations in multiple cancer types
Mutation Induction of Dendrobium 'Earsakul' Using Sodium Azide
Mutations specific to the Rac-GEF domain of TRIO cause intellectual disability and microcephaly
Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa
Mutations in CPAMD8 Cause a Unique Form of Autosomal-Recessive Anterior Segment Dysgenesis
Mutant IP3 receptors attenuate store-operated Ca2+ entry by destabilizing STIM-Orai interactions in Drosophila neurons
Mutations in VP1 and 3A proteins improve binding and replication of rhinovirus C15 in HeLa-E8 cells
Mutations in AGBL5, Encoding alpha-Tubulin Deglutamylase, Are Associated With Autosomal Recessive Retinitis Pigmentosa
Mutation at Expanding Front of Self-Replicating Colloidal Clusters
Mutations in ATOH7 gene in patients with nonsyndromic congenital retinal nonattachment and familial exudative vitreoretinopathy
Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
Mutation analysis by direct and whole exome sequencing in familial and sporadic tooth agenesis
Mutational Analysis in Dystrophin Gene with Dystrophinopathy: A Novel Familial Case Report in Tamil Nadu
Mutational profile of primary dermal melanoma: A case series
Mutation Rate Variation is a Primary Determinant of the Distribution of Allele Frequencies in Humans
Mutations in the Mitochondrial ND1 Gene Are Associated with Postoperative Prognosis of Localized Renal Cell Carcinoma
Mutation in a Highly Conserved COOH-Terminal Residue of Kruppel-Like Factor 1 Associated with Elevated Hb F in a Compound Heterozygous -Thalassemia Patient with a Nontransfusion-Dependent Thalassemia Phenotype
Mutational load of the mitochondrial genome predicts pathological features and biochemical recurrence in prostate cancer
Mutations in NSCLC identified by a next-generation sequencing targeted sequencing panel
Mutations targeting the plug-domain of the Shewanella oneidensis proton-driven stator allow swimming at increased viscosity and under anaerobic conditions
Mutant KRAS Enhances Tumor Cell Fitness by Upregulating Stress Granules
Mutations in the MOV10L1 ATP Hydrolysis Motif Cause piRNA Biogenesis Failure and Male Sterility in Mice
Mutant IDH1 and thrombosis in gliomas
Mutation analysis of a Chinese family with oculocutaneous albinism
Mutation in RET gene: Prophylactic thyroidectomy and postoperative follow-up
Mutation analysis of the PALB2 gene in unselected pancreatic cancer patients in the Czech Republic
Mutations of domain V in 23S ribosomal RNA of macrolide-resistant Mycoplasma gallisepticum isolates in Egypt
Mutational Profile of Metastatic Breast Cancers: A Retrospective Analysis
Mutations in the ERCC2 (XPD) gene associated with severe fetal ichthyosis and dysmorphic features
Mutational Spectrum in Holoprosencephaly Shows That FGF is a New Major Signaling Pathway
Mutator Phenotype and DNA Double-Strand Break Repair in BLM Helicase-Deficient Human Cells
Mutations in mitochondrial DNA regulate mitochondrial diseases and metastasis but do not regulate aging
Mutational analysis of metacaspase CaMca1 and decapping activator Edc3 in the pathogenicity of Candida albicans
Mutational and expressional alterations of ZMPSTE24, DNA damage response-related gene, in gastric and colorectal cancers
Mutation analysis of genes within the dynactin complex in a cohort of hereditary peripheral neuropathies
Mutations in the drug resistance-determining region of Mycobacterium lepromatosis isolated from leprosy patients in Mexico
Mutations Modifying Sporadic Alzheimer's Disease Age of Onset
Mutations in hepatitis B virus small S genes predict postoperative survival in hepatocellular carcinoma
Mutation screening of the SLC26A4 gene in a cohort of 192 Chinese patients with congenital hypothyroidism
Mutation of the Streptococcus gordonii Thiol-Disulfide Oxidoreductase SdbA Leads to Enhanced Biofilm Formation Mediated by the CiaRH Two-Component Signaling System
Mutational analysis of PRNP in Alzheimer's disease and frontotemporal dementia in China
Mutations and altered expression of SERPINF1 in patients with familial otosclerosis
Mutant p53 talks to proteasomes-is there a feedback loop between Nrf2 and mutant p53?
Mutations in PLC delta 1 associated with hereditary leukonychia display divergent PIP2 hydrolytic function
Mutation Spectrum of the PAH Gene in Phenylketonuria Patients in the Karachay-Cherkess Republic (Russia)
Mutations of mtDNA polymerase-gamma and hyperlactataemia in the HIV-infected Zulu population of South Africa
Mutations in the Alpha-D-Galactosidase Gene Suggest Molecular Basis of the Mutant "Makapuno" Coconut (Cocos nucifera L.) Phenomenon
Mutation in the Hair Cell Specific Gene POU4F3 Is a Common Cause for Autosomal Dominant Nonsyndromic Hearing Loss in Chinese Hans
Mutation in Actin-2 Responsible for Megacystis Microcolon Intestinal Hypoperistalsis Syndrome in 4 Chinese Patients
Mutation and screening of neutral protease high-yield strain
Mutation breeding of Saccharomyces cerevisiae with low purine by atmospheric and room temperature plasma
Mutations in DMRT3 affect locomotion in horses and spinal circuit function in mice
Mutation Analysis of NPHS1 in a Worldwide Cohort of Congenital Nephrotic Syndrome Patients
Mutations of Complement Factor I and Potential Mechanisms of Neuroinflammation in Acute Hemorrhagic Leukoencephalitis
Mutation in Cyclophilin B That Causes Hyperelastosis Cutis in American Quarter Horse Does Not Affect Peptidylprolyl cis-trans Isomerase Activity but Shows Altered Cyclophilin B-Protein Interactions and Affects Collagen Folding
Mutant huntingtin impairs immune cell migration in Huntington disease
Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability
Mutation: The History of an Idea from Darwin to Genomics.
Mutable Protection Domains: Adapting System Fault Isolation for Reliability and Efficiency
Mutations of NOTCH1 are an independent predictor of survival in chronic lymphocytic leukemia
Mutants in the Candida glabrata Glycerol Channels Are Sensitized to Cell Wall Stress
Mutations of the AMH Type II Receptor in Two Extended Families with Persistent Mullerian Duct Syndrome: Lack of Phenotype/Genotype Correlation
Mutation Induced Extinction in Finite Populations: Lethal Mutagenesis and Lethal Isolation
Mutations M287L and Q266I in the Glycine Receptor alpha 1 Subunit Change Sensitivity to Volatile Anesthetics in Oocytes and Neurons, but Not the Minimal Alveolar Concentration in Knockin Mice
Mutation analysis of the ATP7B gene in a new group of Wilson%26apos;s disease patients: Contribution to diagnosis
Mutation screening of the EYA1, SIX1, and SIX5 genes in an east asian cohort with branchio-oto-renal syndrome
Mutations in ZIC3 and ACVR2B are a common cause of heterotaxy and associated cardiovascular anomalies
Mutant allele-specific imbalance modulates prognostic impact of KRAS mutations in colorectal adenocarcinoma and is associated with worse overall survival
Mutant p53 protein, master regulator of human malignancies: a report on the fifth Mutant p53 Workshop
Mutation at Positively Selected Positions in the Binding Site for HLA-C Shows That KIR2DL1 Is a More Refined but Less Adaptable NK Cell Receptor Than KIR2DL3
Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome
Mutant NADH dehydrogenase subunit 4 gene delivery to mitochondria by targeting sequence- modified adeno-associated virus induces visual loss and optic atrophy in mice
Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair
Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia
Mutation of Npr2 Leads to Blurred Tonotopic Organization of Central Auditory Circuits in Mice
Mutagenicity of furan in female Big Blue B6C3F1 mice
Mutated Leguminous Lectin Containing a Heparin-Binding like Motif in a Carbohydrate-Binding Loop Specifically Binds to Heparin
Mutations in the Arabidopsis Lst8 and Raptor genes encoding partners of the TOR complex, or inhibition of TOR activity decrease abscisic acid (ABA) synthesis
Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis
Mutant NRAS(Q61) shares signaling similarities across various cancer types - potential implications for future therapies
Mutant COQ2 in Multiple-System Atrophy REPLY
Mutation Profiling in Cholangiocarcinoma: Prognostic and Therapeutic Implications
Mutations in Global Regulators Lead to Metabolic Selection during Adaptation to Complex Environments
Mutation G805R in the transmembrane domain of the LDL receptor gene causes familial hypercholesterolemia by inducing ectodomain cleavage of the LDL receptor in the endoplasmic reticulum
Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD)
Mutational analysis of paediatric patients with tuberous sclerosis complex in Korea: genotype and epilepsy
Mutant IDH1: An immunotherapeutic target in tumors
Mutations in SMARCAD1 cause autosomal dominant adermatoglyphia and perturb the expression of epidermal differentiation-associated genes
Mutation in the X-linked RAB40AL gene (Martin-Probst syndrome) with mental retardation, sensorineural hearing loss, and anomalies of the craniofacies and genitourinary tract: a second case report
Mutational Analysis of Angiogenin Gene in Parkinson's Disease
Mutations in HIV-1 Reverse Transcriptase Affect the Errors Made in a Single Cycle of Viral Replication
Mutations in the Chromodomain-like Insertion of Translation Elongation Factor 3 Compromise Protein Synthesis through Reduced ATPase Activity*
Mutations in RAB39B Cause X-Linked Intellectual Disability and Early-Onset Parkinson Disease with alpha-Synuclein Pathology
Mutations in ROGDI Cause Kohlschutter-Tonz Syndrome
Mutation that causes hypertrophic cardiomyopathy increases force production in human beta-cardiac myosin
Mutational Robustness Accelerates the Origin of Novel RNA Phenotypes through Phenotypic Plasticity
Mutant p53 accumulates in cycling and proliferating cells in the normal tissues of p53 R172H mutant mice
Mutational Landscapes of Sequential Prostate Metastases and Matched Patient Derived Xenografts during Enzalutamide Therapy
Mutations in the Borrelia burgdorferi Flagellar Type III Secretion System Genes fliH and fliI Profoundly Affect Spirochete Flagellar Assembly, Morphology, Motility, Structure, and Cell Division
Mutational and functional analysis of Glucose transporter I deficiency syndrome
Mutations of Cx43 that affect B cell spreading in response to BCR signaling
Mutation and Loss of Expression of ARID1A in Uterine Low-grade Endometrioid Carcinoma
Mutation in the ED1, Ala349Thr in a patient with X-linked hypohidrotic ectodermal dysplasia
Mutations in the beta-tubulin binding site for peloruside A confer resistance by targeting a cleft significant in side chain binding
Mutation in APOA1 predicts increased risk of ischaemic heart disease and total mortality without low HDL cholesterol levels
Mutations in CIC and FUBP1 Contribute to Human Oligodendroglioma
Mutagenic Processing of Ribonucleotides in DNA by Yeast Topoisomerase I
Mutations in lipoprotein lipase that block binding to the endothelial cell transporter GPIHBP1
Mutational Tipping Points for Switching Protein Folds and Functions
Mutasynthesis of a Potent Anticancer Sibiromycin Analogue
Mutations in the basic loop of the Zn binuclear cluster of the UaY transcriptional activator suppress mutations in the dimerisation domain
Mutation of zebrafish Snapc4 is associated with loss of the intrahepatic biliary network
Mutations in the Lamin A/C gene mimic arrhythmogenic right ventricular cardiomyopathy
Mutant PrP Suppresses Glutamatergic Neurotransmission in Cerebellar Granule Neurons by Impairing Membrane Delivery of VGCC alpha(2)delta-1 Subunit
Mutant Flower Morphologies in the Wind Orchid, a Novel Orchid Model Species
Mutant p63 causes defective expansion of ectodermal progenitor cells and impaired FGF signalling in AEC syndrome
Mutant D-amino acid oxidase with higher catalytic efficiency toward D-amino acids with bulky side chains
Mutants of with a change in synthesis of N-acyl-homoserine lactones-Signal molecules of quorum sensing regulation
Mutational spectrum of Smith-Lemli-Opitz syndrome
Mutation in FAM134B causing severe hereditary sensory neuropathy
Mutational analysis of the GYS2 gene in patients diagnosed with ketotic hypoglycaemia
Mutant huntingtin fragmentation in immune cells tracks Huntington%26apos;s disease progression
Mutation analysis of VCP in British familial and sporadic amyotrophic lateral sclerosis patients
Mutagenicity and DNA adduct formation by aristolochic acid in the spleen of Big Blue (R) rats
Mutations of Laurent Polynomials and Flat Families with Toric Fibers
Mutations in the Mediator subunit MED23 link intellectual disability to immediate early gene regulation
Mutations responsible for MYH9-related thrombocytopenia impair SDF-1-driven migration of megakaryoblastic cells
Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome
Mutagenesis, heterogeneous gene expression, and purification and amino acid substitution analyses of plant peroxidase, PrxA3a
Mutation Accumulation in a Selfing Population: Consequences of Different Mutation Rates between Selfers and Outcrossers
Mutated regions of nucleophosmin 1 elicit both CD4(+) and CD8(+) T-cell responses in patients with acute myeloid leukemia
Mutations of the SCN1A gene in acute encephalopathy
Mutational robustness of 16S ribosomal RNA, shown by experimental horizontal gene transfer in Escherichia coli
Mutations Associated with Functional Disorder of Xanthine Oxidoreductase and Hereditary Xanthinuria in Humans
Mutagenesis of the Residues Forming an Ion Binding Pocket of the NtpK Subunit of Enterococcus hirae V-ATPase
Mutational analysis of HRAS and KRAS genes in oral carcinoma cell lines
Mutation of the CYP2R1 Vitamin D 25-Hydroxylase in a Saudi Arabian Family with Severe Vitamin D Deficiency
Mutations in the Sensitive Giant Titin Result in a Broken Heart
Mutation of the translation initiation codon in FGA causes congenital afibrinogenemia
Mutagenesis by an Antisense Oligonucleotide and Its Degradation Product
Mutations of ventricular essential myosin light chain disturb myosin binding and sarcomeric sorting
Mutations and Natural Selection in the Protein World
Mutational analysis of the VCP gene in Parkinson%26apos;s disease
Mutation analysis of the optineurin gene in familial amyotrophic lateral sclerosis
Mutations in C12orf62, a Factor that Couples COX I Synthesis with Cytochrome c Oxidase Assembly, Cause Fatal Neonatal Lactic Acidosis
Mutations in SRCAP, Encoding SNF2-Related CREBBP Activator Protein, Cause Floating-Harbor Syndrome
Mutated Intramolecular Chaperones Generate High-Activity Isomers of Mature Enzymes
Mutation spectrum in the French cohort of galactosemic patients and structural simulation of 27 novel missense variations
Mutations in UVSSA cause UV-sensitive syndrome and destabilize ERCC6 in transcription-coupled DNA repair
Mutational Spectrum in the Ca2+-Activated Cation Channel Gene TRPM4 in Patients with Cardiac Conductance Disturbances
Mutation of HSP110 in colorectal cancer: the chaperone paradox
Mutation analysis of the GLUT2 gene in three unrelated Egyptian families with Fanconi-Bickel syndrome: revisited gene atlas for renumbering
Mutations in MECP2 exon 1 in classical rett patients disrupt MECP2_e1 transcription, but not transcription of MECP2_e2
Mutational screening of THAP1 in a German population with primary dystonia
Mutation load under spatial variation Variation in selective intensity over space alters classic mutation load predictions
Mutans Streptococci and Lactobacilli Colonization in Predentate Children from the Neonatal Period to Seven Months of Age
Mutation specific antibodies: tool or dinosaur?
Mutational Inactivation of STAG2 Causes Aneuploidy in Human Cancer
Mutations of human cytochrome P450 reductase differentially modulate heme oxygenase-1 activity and oligomerization
Mutagenesis Mapping of the Presenilin 1 Calcium Leak Conductance Pore
Mutation of NIMA-related kinase 1 (NEK1) leads to chromosome instability
Mutation analysis and evaluation of the cardiac localization of TMEM43 in arrhythmogenic right ventricular cardiomyopathy
Mutations of the hexose-6-phosphate dehydrogenase gene rarely cause hyperandrogenemic polycystic ovary syndrome
Mutations in the NKX2.5 Gene and the PAX8 Promoter in a Girl with Thyroid Dysgenesis
Mutational analysis of D2HGDH and L2HGDH in brain tumours without IDH1 or IDH2 mutations
Mutation and gender-specific risk in type 2 long QT syndrome: Implications for risk stratification for life-threatening cardiac events in patients with long QT syndrome
Mutation in the beta A3/A1-crystallin gene impairs phagosome degradation in the retinal pigmented epithelium of the rat
Mutant p53(R175H) upregulates Twist1 expression and promotes epithelial-mesenchymal transition in immortalized prostate cells
Mutant p53 oncogenic functions are sustained by Plk2 kinase through an autoregulatory feedback loop
Mutant p53 gain of function is interwoven into the hallmarks of cancer
Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss
Mutational Specificities of Brominated DNA Adducts Catalyzed by Human DNA Polymerases
Mutations in RLBP1 associated with fundus albipunctatus in consanguineous Pakistani families
Mutations in the beta-subunit of rod phosphodiesterase identified in consanguineous Pakistani families with autosomal recessive retinitis pigmentosa
Mutational analysis of the EMCV 2A protein identifies a nuclear localization signal and an eIF4E binding site
Mutated C-terminal fragments of Clostridium perfringens enterotoxin have increased affinity to claudin-4 and reversibly modulate tight junctions in vitro
Mutations in Iron-Sulfur Cluster Scaffold Genes NFU1 and BOLA3 Cause a Fatal Deficiency of Multiple Respiratory Chain and 2-Oxoacid Dehydrogenase Enzymes
Mutation analysis of the PALB2 cancer predisposition gene in familial melanoma
Mutagenicity of Carbon Nanomaterials
Mutation in subdomain G' of mitochondrial elongation factor G1 is associated with combined OXPHOS deficiency in fibroblasts but not in muscle
Mutant ataxin-3 promotes the autophagic degradation of parkin
Mutations in the autoinflammatory cryopyrin-associated periodic syndrome gene: epidemiological study and lessons from eight years of genetic analysis in France
Mutation Nomenclature in Practice: Findings and Recommendations from the Cystic Fibrosis External Quality Assessment Scheme
Mutation analysis of KRAS prior to targeted therapy in colorectal cancer: development and evaluation of quality by a European external quality assessment scheme
Mutations and Deletions in PCDH19 Account for Various Familial or Isolated Epilepsies in Females
Mutations in Nicastrin Protein Differentially Affect Amyloid beta-Peptide Production and Notch Protein Processing
Mutational analysis of wheat (Triticum aestivum L.) nucleotide pyrophosphatase/phosphodiesterase shows the role of six amino acids in the catalytic mechanism
Mutational analysis of calnexin
Mutations in LRRK2 increase phosphorylation of peroxiredoxin 3 exacerbating oxidative stress-induced neuronal death
Mutations in NMDA receptors influence neurodevelopmental disorders causing epilepsy and intellectual disability
Mutations in a novel cilia-centrosome protein cause a cystic kidney disease associated with retinal degeneration
Mutations Suppressing the Loss of DegQ Function in Bacillus subtilis (natto) Poly-gamma-Glutamate Synthesis
Mutations Targeting the C-Terminal Domain of FliG Can Disrupt Motor Assembly in the Na+-Driven Flagella of Vibrio alginolyticus
Mutation in the beta adducin subunit causes tissue-specific damage to myogenic tone
Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome
Mutations That Replace Aromatic Side Chains Promote Aggregation of the Alzheimer's A beta Peptide
Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability
Mutational Analysis of the Transmembrane Helix 2-HAMP Domain Connection in the Escherichia coli Aspartate Chemoreceptor Tar
Mutation in SAM Domain of TP63 is Associated With Nonsyndromic Cleft Lip and Palate and Cleft Palate
MutaDATABASE: a centralized and standardized DNA variation database
Mutation Rates across Budding Yeast Chromosome VI Are Correlated with Replication Timing
Mutation of HIV-1 Genomes in a Clinical Population Treated with the Mutagenic Nucleoside KP1461
Mutations in the RAS/RAF/MAP Kinase Pathway Commonly Occur in Gallbladder Adenomas But Are Uncommon in Gallbladder Adenocarcinomas
Mutation that blocks ATP binding creates a pseudokinase stabilizing the scaffolding function of kinase suppressor of Ras, CRAF and BRAF
Mutations of beta-tubulin codon 198 or 200 indicate thiabendazole resistance among isolates of Penicillium digitatum collected from citrus in Taiwan
Mutations of beta-tubulin codon 198 or 200 indicate thiabendazole resistance among isolates of Penicillium digitatum collected from citrus in Taiwan (vol 150, pg 157, 2011)
Mutational analysis of type III effector genes from Xanthomonas citri subsp citri
Mutations in the nucleotide binding pocket of MreB can alter cell curvature and polar morphology in Caulobacter
Mutation Distribution in Expanded Screening for Cystic Fibrosis: Making Up the Balance in a Context of Ethnic Diversity
Mutation in the factor VII hepatocyte nuclear factor 4 alpha-binding site contributes to factor VII deficiency
Mutator Suppression and Escape from Replication Error-Induced Extinction in Yeast
Mutations in or near the Transmembrane Domain Alter PMEL Amyloid Formation from Functional to Pathogenic
Mutator dynamics in sexual and asexual experimental populations of yeast
Mutations of the Same Conserved Glutamate Residue in NBD2 of the Sulfonylurea Receptor 1 Subunit of the K-ATP Channel Can Result in Either Hyperinsulinism or Neonatal Diabetes
Mutation scanning-coupled sequencing of nuclear ribosomal DNA spacers as a tool for the specific identification of different Contracaecum (Nematoda: Anisakidae) larval types
Mutagenesis and subsite mapping underpin the importance for substrate specificity of the aglycon subsites of glycoside hydrolase family 11 xylanases
Mutations in DHDPSL Are Responsible For Primary Hyperoxaluria Type III
Mutations in the Hyperosmotic Stress-Responsive Mitochondrial BASIC AMINO ACID CARRIER2 Enhance Proline Accumulation in Arabidopsis
Mutations in SOHLH1 Gene Associate with Nonobstructive Azoospermia
Mutations in agr Do Not Persist in Natural Populations of Methicillin-Resistant Staphylococcus aureus
Mutant cells defective in DNA repair pathways provide a sensitive high-throughput assay for genotoxicity
Mutation in utp15 Disrupts Vascular Patterning in a p53-Dependent Manner in Zebrafish Embryos
Mutation of Glutamine to Arginine at Position 548 of IE2 86 in Human Cytomegalovirus Leads to Decreased Expression of IE2 40, IE2 60, UL83, and UL84 and Increased Transcription of US8-9 and US29-32
Mutant cycles at CFTR's non-canonical ATP-binding site support little interface separation during gating
Mutation of the 5 '-Untranslated Region Stem-Loop Structure Inhibits alpha 1(I) Collagen Expression in Vivo
Mutations of the Listeria monocytogenes Peptidoglycan N-Deacetylase and O-Acetylase Result in Enhanced Lysozyme Sensitivity, Bacteriolysis, and Hyperinduction of Innate Immune Pathways
Mutationally Activated BRAF(V600E) Elicits Papillary Thyroid Cancer in the Adult Mouse
Mutations in RIPK4 Cause the Autosomal-Recessive Form of Popliteal Pterygium Syndrome
Mutation of Rubie, a Novel Long Non-Coding RNA Located Upstream of Bmp4, Causes Vestibular Malformation in Mice
Mutations of puzzles and equivariant cohomology of two-step flag varieties
Mutational Heterogeneity in Melanoma: An Inconvenient Truth
Mutational analysis of the N-terminal domain of UreR, the positive transcriptional regulator of urease gene expression
Mutations in Cytoplasmic Loops of the KCNQ1 Channel and the Risk of Life-Threatening Events Implications for Mutation-Specific Response to beta-Blocker Therapy in Type 1 Long-QT Syndrome
Mutational analysis of Trypanosoma brucei editosome proteins KREPB4 and KREPB5 reveals domains critical for function
Mutation Spectra of S-(2-Hydroxy-3,4-epoxybutyl)glutathione: Comparison with 1,3-Butadiene and Its Metabolites in the Escherichia coli rpoB Gene
Mutational analysis of NOG in esophageal atresia and tracheoesophageal fistula patients
Mutational Robustness of an RNA Virus Influences Sensitivity to Lethal Mutagenesis
Mutant p53 subverts PLK2 function in a novel, reinforced loop of corruption
Mutagenesis of Isopentenyl Phosphate Kinase To Enhance Geranyl Phosphate Kinase Activity
Mutation scanning-based analysis of Theileria orientalis populations in cattle following an outbreak
Mutations in the soybean 3-ketoacyl-ACP synthase gene are correlated with high levels of seed palmitic acid
Mutant LV476-7 AA of A-subunit of Enterococcus hirae V-1-ATPase: High affinity of A(3)B(3) complex to DF axis and low ATPase activity
Mutation-Positive Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: The Triangle of Dysplasia Displaced
Mutations of FLT3/ITD confer resistance to multiple tyrosine kinase inhibitors
Mutations in the PFN1 gene are not a common cause in patients with amyotrophic lateral sclerosis and frontotemporal lobar degeneration in France
Mutational and putative neoantigen load predict clinical benefit of adoptive T cell therapy in melanoma
Mutations Located outside the Integrase Gene Can Confer Resistance to HIV-1 Integrase Strand Transfer Inhibitors
Mutation of NRAS is a rare genetic event in ovarian low-grade serous carcinoma
Mutation Clusters from Cancer Exome
Mutations in the X-linked ATP6AP2 cause a glycosylation disorder with autophagic defects
Mutational Correlates of Virological Failure in Individuals Receiving a WHO-Recommended Tenofovir-Containing First-Line Regimen: An International Collaboration
Mutation of the SP1 gene is responsible for the small-panicle trait in the rice cultivar Tachisuzuka, but not necessarily for high sugar content in the stem
Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia
Mutational analysis of multiple lung cancers: Discrimination between primary and metastatic lung cancers by genomic profile
Mutation-specific downregulation of CFTR2 variants by gating potentiators
Mutational burden, immune checkpoint expression, and mismatch repair in glioma: implications for immune checkpoint immunotherapy
Mutations in Histone Acetylase Modifier BRPF1 Cause an Autosomal-Dominant Form of Intellectual Disability with Associated Ptosis
Mutations in folate transporter genes and risk for human myelomeningocele
Mutant RUNX1 and histone tales
Mutants of the Flavoprotein iLOV as Prospective Red-Shifted Fluorescent Markers
Mutations in BMPR2 are not present in patients with pulmonary hypertension associated with congenital diaphragmatic hernia
Mutagenic potential of nitrogen mustard-induced formamidopyrimidine DNA adduct: Contribution of the non-canonical -anomer
Mutant cycle analysis identifies a ligand interaction site in an odorant receptor of the malaria vector Anopheles gambiae
Mutations of KIF5C cause a neurodevelopmental disorder of infantile-onset epilepsy, absent language, and distinctive malformations of cortical development
Mutations in SDR9C7 gene encoding an enzyme for vitamin A metabolism underlie autosomal recessive congenital ichthyosis
Mutation-Induced Changes in the Protein Environment and Site Energies in the (M)L214G Mutant of the Rhodobacter sphaeroides Bacterial Reaction Center
Mutation-adapted U1 snRNA corrects a splicing error of the dopa decarboxylase gene
Mutations in chromatin machinery and pediatric high-grade glioma
Mutations in GAS8, a Gene Encoding a Nexin-Dynein Regulatory Complex Subunit, Cause Primary Ciliary Dyskinesia with Axonemal Disorganization
Mutational pattern of a sample from a critical branching population
Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness
Mutations of the RTEL1 Helicase in a Hoyeraal-Hreidarsson Syndrome Patient Highlight the Importance of the ARCH Domain
Mutational spectrum of intraepithelial neoplasia in pancreatic heterotopia
Mutational Analysis of Prostate-Specific Antigen Defines the Intrinsic Proteolytic Activity of the proPSA Zymogen
Mutation spectrum of POLE and POLD1 mutations in South East Asian women presenting with grade 3 endometrioid endometrial carcinomas
Mutational Processes Shaping the Genome in Early Human Embryos
Mutational analysis of ITPR1 in a Taiwanese cohort with cerebellar ataxias
Mutations in KIAA0753 cause Joubert syndrome associated with growth hormone deficiency
Mutagenic Effects of Iron Oxide Nanoparticles on Biological Cells
Mutations in the ABCG8 gene are associated with sitosterolaemia in the homozygous form and xanthelasmas in the heterozygous form
Mutations in the Fusion Protein of Measles Virus That Confer Resistance to the Membrane Fusion Inhibitors Carbobenzoxy-D-Phe-L-Phe-Gly and 4-Nitro-2-Phenylacetyl Amino-Benzamide
Mutations in DDHD1, encoding a phospholipase A1, is a novel cause of retinopathy and neurodegeneration with brain iron accumulation
Mutation Rate Evolution in Partially Selfing and Partially Asexual Organisms
Mutations in GFPT1-related congenital myasthenic syndromes are associated with synaptic morphological defects and underlie a tubular aggregate myopathy with synaptopathy
Mutant IDH1 expression is associated with down-regulation of monocarboxylate transporters
Mutation of p53 Gene and Its Correlation with the Clinical Outcome in Dogs with Lymphoma
Mutagenicity of Cigarette Butt Waste in the Bacterial Reverse Mutation Assay: The Protective Effects of beta-Caryophyllene and beta-Caryophyllene Oxide
Mutational landscape of lacrimal gland carcinomas and implications for treatment
Mutations in Linkage Disequilibrium With Putative Disease-Causing Mutations
Mutational Analysis of the Rift Valley Fever Virus Glycoprotein Precursor Proteins for Gn Protein Expression
Mutant p53 in Concert With an Interleukin-27 Receptor Alpha Deficiency Causes Spontaneous Liver Inflammation, Fibrosis, and Steatosis in Mice
Mutations of Chromatin Structure Regulating Genes in Human Malignancies
Mutation of the rice 21 predicted nuclear localization sequence does not affect resistance to Xanthomonas oryzae pv. oryzae
Mutations Associated with Acquired Resistance to PD-1 Blockade in Melanoma
Mutations in TFAM, encoding mitochondrial transcription factor A, cause neonatal liver failure associated with mtDNA depletion
Mutations in NONO gene lead to syndromic intellectual disability and inhibitory synaptic defects
Mutational Consequences of Ciprofloxacin in Escherichia coli
Mutagen Synergy: Hypermutability Generated by Specific Pairs of Base Analogs
Mutation in the Human HPRT1 Gene and the Lesch-Nyhan Syndrome
Mutations in the polyglutamylase gene TTLL5, expressed in photoreceptor cells and spermatozoa, are associated with cone-rod degeneration and reduced male fertility
Mutators, Generalized Impedance Converters and Inverters, and Their Realization Using Generalized Current Conveyors
Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families
Mutations in the 5 ' UTR of ANKRD26, the Ankirin Repeat Domain 26 Gene, Cause an Autosomal-Dominant Form of Inherited Thrombocytopenia, THC2
Mutation of conserved tryptophan residues at the dimer interface of Staphylococcus aureus nitric oxide synthase
Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with Intellectual Disability
Mutation analysis of the TNFAIP3 (A20) tumor suppressor gene in CLL
Mutation of a diacidic motif in SIV-PBj Nef impairs T-cell activation and enteropathic disease
Mutation Analysis Ion Channel Genes Ventricular Fibrillation Survivors with Coronary Artery Disease
Mutation in IFT80 in a fetus with the phenotype of Verma-Naumoff provides molecular evidence for Jeune-Verma-Naumoff dysplasia spectrum
Mutations in the Dimer Interface of Dihydrolipoamide Dehydrogenase Promote Site-specific Oxidative Damages in Yeast and Human Cells
Mutagenic Analysis of hPNMT Confirms the Importance of Lys57 and the Inhibitor Binding Site
Mutational analysis for biotinidase deficiency of a Greek patients' cohort ascertained through expanded newborn screening
Mutations for Leber hereditary optic neuropathy in patients with alcohol and tobacco optic neuropathy
Mutation in the sdeS Gene Promotes Expression of the sdeAB Efflux Pump Genes and Multidrug Resistance in Serratia marcescens
Mutations of CD79A, CD79B and EZH2 genes in immunodeficiency-related non-Hodgkin lymphomas
Mutations in CYP24A1 and Idiopathic Infantile Hypercalcemia
Mutation in a mitochondrial ribosomal protein causes increased sensitivity to oxygen with decreased longevity in the nematode Caenorhabditis elegans
Mutant Prourokinase with Adjunctive C1-Inhibitor Is an Effective and Safer Alternative to tPA in Rat Stroke
Mutation spectrum of phenylketonuria in Iranian population
Mutational Analysis of Catecholamine Binding in Tyrosine Hydroxylase
Mutations in beta ' subunit of Escherichia coli RNA polymerase perturb the activator polymerase functional interaction required for promoter clearance
Mutated hybrid inflation in f(R, square R)-gravity
Mutations in TGFBR2 gene cause spontaneous cervical artery dissection
Mutagenesis Objective Search and Selection Tool (MOSST): an algorithm to predict structure-function related mutations in proteins
Mutations of ACADS Gene Associated with Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency
Mutational Analysis of Splicing Activities of Ribonucleotide Reductase alpha Subunit Protein from Lytic Bacteriophage P1201
Mutational effects of the consensus aromatic residues in the mRNA capping domain of Bamboo mosaic virus on GTP methylation and virus accumulation
Mutational analysis of kinetic partitioning in protein folding and protein-DNA binding
Mutations in methylenetetrahydrofolate reductase and in cysthationine beta synthase: is there a link to homocysteine levels in peripheral arterial disease?
Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and flies
Mutants of beta-strand beta 3 and the loop B in the interface between alpha 7 subunits of a homomeric acetylcholine receptor show functional and pharmacological alterations
Mutation analysis of PMP22 in Slovak patients with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies
Mutations in 16S rRNA that suppress cold-sensitive initiation factor 1 affect ribosomal subunit association
Mutated variant of Candida antarctica lipase B in (S)-selective dynamic kinetic resolution of secondary alcohols
Mutations in INF2 Are a Major Cause of Autosomal Dominant Focal Segmental Glomerulosclerosis
Mutations in disguise
Mutations and Pituitary Morphology in a Series of 82 Patients with PROP1 Gene Defects
Mutation Screening of the GJA7 (Cx45) Gene in a Large International Series of Probands with Nonsyndromic Hearing Impairment
Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia
Mutation rate of bacteriophage Phi X174 modified through changes in GATC sequence context
Mutagenic potential and modulatory effects of the medicinal plant Luehea divaricata (Malvaceae) in somatic cells of Drosophila melanogaster: SMART/wing
Mutation and Expression Analyses of the Ribosomal Protein Gene RPL10 in an Extended German Sample of Patients With Autism Spectrum Disorder
Mutagenic assessment of Prestige fuel oil spilled on the shore and submitted to field trials of bioremediation
Mutations of calcium-sensing receptor gene: two novel mutations and overview of impact on calcium homeostasis
Mutations in bone morphogenetic protein 15 and growth differentiation factor 9 genes are associated with increased litter size in fat-tailed sheep breeds
Mutations in the NKX2-5 gene in patients with stroke and patent foramen ovale (vol 111, pg 574, 2009)
Mutations in the genes coding for the NF-kappa B regulating factors I kappa B alpha and A20 are uncommon in nodular lymphocyte-predominant Hodgkin's lymphoma
Mutations of CARD11 but not TNFAIP3 may activate the NF-kappa B pathway in primary CNS lymphoma
Mutagenesis of tGCN5 core region reveals two critical surface residues F90 and R140
Mutation accumulation in Tetrahymena
Mutation in erythroid specific transcription factor KLF1 causes Hereditary Spherocytosis in the Nan hemolytic anemia mouse model
Mutation of WRKY transcription factors initiates pith secondary wall formation and increases stem biomass in dicotyledonous plants
Mutational spectrum of cystic fibrosis in the Lebanese population
Mutants of the Saccharomyces cerevisiae VPS genes CCZ1 and YPT7 are blocked in different stages of sporulation
Mutation classes of diagrams via infinite graphs
Mutated p.4894 RyR1 Function Related to Malignant Hyperthermia and Congenital Neuromuscular Disease with Uniform Type 1 Fiber (CNMDU1)
Mutagenicity of secondary oxidation products of 8-oxo-7,8-dihydro-2 '-deoxyguanosine 5 '-triphosphate (8-hydroxy-2 '- deoxyguanosine 5 '-triphosphate)
Mutation and Copy Number Analysis in Paroxysmal Kinesigenic Dyskinesia Families
Mutation analysis of the growth factor genes PlGF, Flt1, IGF-I, and IGF-IR in intrauterine growth restriction with abnormal placental blood flow
Mutations in TGFbeta-RII and BAX mediate tumor progression in the later stages of colorectal cancer with microsatellite instability
Mutations in the stereospecificity pocket and at the entrance of the active site of Candida antarctica lipase B enhancing enzyme enantioselectivity
Mutational analysis of K-ras codon 12 in blood samples of patients with acute myeloid leukemia
Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease
Mutational study of the HSPA2 gene in infertile patients and controls
Mutation of CANT1 Causes Desbuquois Dysplasia
Mutations in PTPRQ Are a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB84 and Associated with Vestibular Dysfunction
Mutational analysis of active-site residues in the Mycobacterium leprae RecA intein, a LAGLIDADG homing endonuclease: Asp(122) and Asp(193) are crucial to the double-stranded DNA cleavage activity whereas Asp(218) is not
Mutation scanning of exon 20 of the BRCA1 gene by high-resolution melting curve analysis
Mutation Screening of the EYA1, SIX1, and SIX5 Genes in a Large Cohort of Patients Harboring Branchio-oto-Renal Syndrome Calls into Question the Pathogenic Role of SIX5 Mutations
Mutagenesis-Based Evidence for an Asymmetric Configuration of the Ring-Shaped Transcription Termination Factor Rho
Mutagenic and morphologic impacts of 1.8 GHz radiofrequency radiation on human peripheral blood lymphocytes (hPBLs) and possible protective role of pre-treatment with Ginkgo biloba (EGb 761)
Mutations in the E2 and NS5A Regions in Patients Infected With Hepatitis C Virus Genotype 1a and Their Correlation With Response to Treatment
Mutations in the TSPAN12 Gene in Japanese Patients with Familial Exudative Vitreoretinopathy
Mutational analyses of Cry protein block7 polypeptides that facilitate the formation of protein inclusion in Escherichia coli
Mutation Screening of the GUCA1B Gene in Patients with Autosomal Dominant Cone and Cone Rod Dystrophy
Mutations in the transmembrane domain M3 generate spontaneously open orphan glutamate delta 1 receptor
Mutational Effects and Population Dynamics During Viral Adaptation Challenge Current Models
Mutation of a C-Terminal Motif Affects Kaposi's Sarcoma-Associated Herpesvirus ORF57 RNA Binding, Nuclear Trafficking, and Multimerization
Mutation-periodic quivers, integrable maps and associated Poisson algebras
Mutation of GOGAT prevents pea bacteroid formation and N-2 fixation by globally downregulating transport of organic nitrogen sources
Mutational Patterns in RNA Secondary Structure Evolution Examined in Three RNA Families
Mutable objects in R
Mutagenesis of the L, M, and N Subunits of Complex I from Escherichia coli Indicates a Common Role in Function
Mutant Profilin Suppresses Mutant Actin-dependent Mitochondrial Phenotype in Saccharomyces cerevisiae
Mutacins from Streptococcus mutans UA159 Are Active against Multiple Streptococcal Species
Mutations That Probe the Cooperative Assembly of O-6-Alkylguanine-DNA Alkyltransferase Complexes
Mutation screening of mitofusin 2 in Charcot-Marie-Tooth disease type 2
Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegia
Mutagenesis of Critical Amino Acid Residues in alpha-Helix and beta-Sheet Structures of Brazzein
Mutational analysis in RNAs: comparing programs for RNA deleterious mutation prediction
Mutation of isoleucine 705 of the oxidosqualene-lanosterol cyclase from Saccharomyces cerevisiae affects lanosterol's C/D-ring cyclization and 17 alpha/beta-exocyclic side chain stereochemistry
Mutational analysis of the HIPK2 gene in keratoacanthoma and squamous cell carcinoma of the skin
Mutational analysis of RUNX1T1 gene in acute leukemias, breast and lung carcinomas
Mutational and expressional analysis of a haploinsufficient tumor suppressor gene DOK2 in gastric and colorectal cancers
Mutational Screening of the BRCA1 Gene in Sporadic Breast Cancer in Kazakhstan Population
Mutations in Two PKR-Binding Domains in Chronic Hepatitis C of Genotype 3a and Correlation With Viral Loads and Interferon Responsiveness
Mutation and haplotype analysis of oculopharyngeal muscular dystrophy in Thai patients
Mutational analysis of mononucleotide repeats in XRCC2 and XRCC6 in cancers with microsatellite instability
Mutational and expressional analyses of ATG5, an autophagy-related gene, in gastrointestinal cancers
Mutational analysis of mononucleotide repeats in HDAC4, 5, 6, 7, 9 and 11 genes in gastric and colorectal carcinomas with microsatellite instability
Mutational analysis of the extracellular domain of ERBB4 gene in common carcinomas
Mutational analysis of NCOA2 gene in prostate cancer and other common cancers
Mutations in the core and NS5A region of hepatitis C virus genotype 1b and correlation with response to pegylated-interferon-alpha 2b and ribavirin combination therapy
Mutations in CDON, Encoding a Hedgehog Receptor, Result in Holoprosencephaly and Defective Interactions with Other Hedgehog Receptors
Mutans streptococci colonization associates with the occupation of caretaker, a practise-based study
Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability (vol 89, pg 176, 2011)
Mutational study in the PDHA1 gene of 40 patients suspected of pyruvate dehydrogenase complex deficiency
Mutations in the Carboxyl-terminal SEC24 Binding Motif of the Serotonin Transporter Impair Folding of the Transporter
Mutations in the second zinc finger of human EKLF reduce promoter affinity but give rise to benign and disease phenotypes
Mutagenesis of tyrosine residues within helix VII in subunit I of the cytochrome cbb (3) oxidase from Rhodobacter capsulatus
Mutation testing on an object-oriented framework: An experience report
Mutation Screening of the CHCHD2 Gene for Alzheimer's Disease and Frontotemporal Dementia in Chinese Mainland Population
钼钛锆合金材料特殊型腔的组合放电加工方法的研究
Mutations of Epigenetic Modifier Genes as a Poor Prognostic Factor in Acute Promyelocytic Leukemia Under Treatment With All-Trans Retinoic Acid and Arsenic Trioxide
Mutation in the THPO gene is not associated with aplastic anaemia in Japanese children
Mutations of the SH3BP2 Gene in 2 Families of Cherubism
Mutants of Lactobacillus plantarum ML11-11 Deficient in Co-Aggregation with Yeast Exhibited Reduced Activities of Mixed-Species Biofilm Formation
Mutational Analysis of a CBM Family 5 Chitin-Binding Domain of an Alkaline Chitinase from Bacillus sp J813
Mutation of alpha-tubulin genes in trifluralin-resistant water foxtail (Alopecurus aequalis)
Mutations of the Potassium Channel KCNJ5 Causing Aldosterone-Producing Adenomas One or Two Hits?
Mutation at the Human D1S80 Minisatellite Locus
Mutant and Overexpression Analysis of a C2H2 Single Zinc Finger Gene of Arabidopsis
Mutation-selection balance and mixed mating with asexual reproduction
Mutation of a Positively Charged Cytoplasmic Motif within CD1d Results in Multiple Defects in Antigen Presentation to NKT Cells
Mutagenicity and Oral Toxicity Studies of Terminalia chebula
Mutant prevention concentration and phenotypic and molecular basis of fluoroquinolone resistance in clinical isolates and in vitro-selected mutants of Escherichia coli from dogs
Mutation Accumulation May Be a Minor Force in Shaping Life History Traits
Mutation Accumulation May Only Be a Minor Force in Shaping Life-History Traits, Even when Reproduction Is Sexual
Mutant flu: assessing biosecurity risks
Mutations within the human parainfluenza virus type 3 (HPIV 3) C protein affect viral replication and host interferon induction
Mutation screening of RET proto-oncogene in a family with medullary thyroid carcinoma, marfanoid habitus and pheochromocytoma; from clinically MEN2B to genetically MEN2A syndrome
Mutant human myocilin induces strain specific differences in ocular hypertension and optic nerve damage in mice
Mutation C3256T of Mitochondrial Genome in White Blood Cells: Novel Genetic Marker of Atherosclerosis and Coronary Heart Disease
Mutation analysis in 54 propionic acidemia patients
Mutational, proteomic and metabolomic analysis of a plant growth promoting copper-resistant Pseudomonas spp.
Mutation Analysis of Barley Malt Protein Z4 and Protein Z7 on Beer Foam Stability
Mutation of ATF4 mediates resistance of neuronal cell lines against oxidative stress by inducing xCT expression
Mutagenicity of Ochratoxin A and Its Hydroquinone Metabolite in the SupF Gene of the Mutation Reporter Plasmid Ps189
Mutational Analysis of Cvab, an ABC Transporter Involved in the Secretion of Active Colicin V
Mutations of ATIC and ADSL affect purinosome assembly in cultured skin fibroblasts from patients with AICA-ribosiduria and ADSL deficiency
Mutation-Driven Generation of Unit Tests and Oracles
Mutational analysis of VCP gene in familial amyotrophic lateral sclerosis
Mutational and haplotype map of NOTCH3 in a cohort of Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
Mutations in hpyAVIBM, C5 cytosine DNA methyltransferase from Helicobacter pylori result in relaxed specificity
Mutational analysis of cysteine 328 and cysteine 368 at the interface of Plasmodium falciparum adenylosuccinate synthetase
Mutations in Escherichia coli aceE and ribB Genes Allow Survival of Strains Defective in the First Step of the Isoprenoid Biosynthesis Pathway
Mutations in the protease gene associated with virological failure to lopinavir/ritonavir-containing regimens
Mutation and SL(2, C)-Reidemeister torsion for hyperbolic knots
Mutations in Radial Spoke Head Genes and Ultrastructural Cilia Defects in East-European Cohort of Primary Ciliary Dyskinesia Patients
Mutations of the Serine Protease CAP1/Prss8 Lead to Reduced Embryonic Viability, Skin Defects, and Decreased ENaC Activity
Mutations in DYNC1H1 cause severe intellectual disability with neuronal migration defects
Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease
Mutagenesis-Mediated Virus Extinction: Virus-Dependent Effect of Viral Load on Sensitivity to Lethal Defection
Mutation analysis of cerebrotendinous xanthomatosis in an Indian case
Mutations and deletions of ARID1A in breast tumors
Mutagenic effect of freezing on nuclear DNA of Saccharomyces cerevisiae
Mutagenic activity of peloids in the Salmonella Ames test
Mutants in Drosophila TRPC Channels Reduce Olfactory Sensitivity to Carbon Dioxide
Mutations in NNT encoding nicotinamide nucleotide transhydrogenase cause familial glucocorticoid deficiency
Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients
Mutagenic Bypass of 8-Oxo-7,8-dihydroguanine (8-Hydroxyguanine) by DNA Polymerase kappa in Human Cells
Mutation in a valine residue induces drastic changes in 3D structure of human prion protein
Mutational Patterns and Novel Mutations of the BRAF Gene in a Large Cohort of Korean Patients with Papillary Thyroid Carcinoma
Mutational and expressional analyses of STAG2 gene in solid cancers
Mutational analysis of tumour suppressor gene NF2 in common solid cancers and acute leukaemias
Mutational analysis of Mdm2 C-terminal tail suggests an evolutionarily conserved role of its length in Mdm2 activity toward p53 and indicates structural differences between Mdm2 homodimers and Mdm2/MdmX heterodimers
Mutagen-mediated enhancement of HIV-1 replication in persistently infected cells
Mutational analysis of the feline CLN3 gene and an ultrastructural evaluation of lysosomal storage materials in a cat with neuronal ceroid lipofuscinosis: An investigation into the molecular basis of the disease
Mutation analysis of GM1 gangliosidosis in a Siamese cat from Japan in the 1960s
Mutations in the gyrA and parC genes and in vitro activities of fluoroquinolones in 114 clinical isolates of Pseudomonas aeruginosa derived from urinary tract infections and their rapid detection by denaturing high-performance liquid chromatography
Mutational Analysis of the T4 Gp59 Helicase Loader Reveals Its Sites for Interaction with Helicase, Single-stranded Binding Protein, and DNA
Mutagenicity of Sediment Samples from Nif Brook (Western Turkey)
Mutation in RAB33B, which encodes a regulator of retrograde Golgi transport, defines a second Dyggve-Melchior-Clausen locus
Mutational Analysis in N- and C- Termini of RB1 Gene among Sporadic Retinoblastoma Patients in Malaysia
Mutans Streptococci and Caries Prevalence in Children after Early Maternal Caries Prevention: A Follow-Up at 19 Years of Age
Mutations selected in the hepatitis C virus NS3 protease domain during sequential treatment with boceprevir with and without pegylated interferon alfa-2b
Mutation rate in Velvet tobacco mottle virus varies between genomic region and virus variant but is not influenced by obligatory mirid transmission
Mutation analysis of the methylmalonyl-CoA mutase gene in ten Mexican patients with methylmalonic acidemia
Mutational Analysis of the NPHS2 Gene in Czech Patients with Idiopathic Nephrotic Syndrome
Mutations in WNT10A are present in more than half of isolated hypodontia cases
Mutation detection in GJB2 gene among Malays with non-syndromic hearing loss
Mutation based test case generation via a path selection strategy
Mutation spectrum and phenotypic manifestation in FSHD Greek patients
Mutation of Glu(521) or Glu(535) in Cytoplasmic Loop 5 Causes Differential Misfolding in Multiple Domains of Multidrug and Organic Anion Transporter MRP1 (ABCC1)
Mutant GBA1 Expression and Synucleinopathy Risk: First Insights from Cellular and Mouse Models
Mutation of the Sensor Kinase chvG in Rhizobium leguminosarum Negatively Impacts Cellular Metabolism, Outer Membrane Stability, and Symbiosis
Mutational status predicts the risk of thromboembolic events in lung adenocarcinoma
Mutation of Gly195 of the ChIH Subunit of Mg-chelatase Reduces Chlorophyll and Further Disrupts PS II Assembly in a Ycf48-Deficient Strain of Synechocystis sp PCC 6803
Mutant p53 sIL-1Ra
Mutation, Witten index, and quiver invariant
Mutations Proximal to Sites of Autoproteolysis and the alpha-Helix That Co-evolve under Drug Pressure Modulate the Autoprocessing and Vitality of HIV-1 Protease
Mutation Drivers of Immunological Responses to Cancer
Mutations in Complex I Assembly Factor TMEM126B Result in Muscle Weakness and Isolated Complex I Deficiency
Mutant p53 Protein and the Hippo Transducers YAP and TAZ: A Critical Oncogenic Node in Human Cancers
Mutational analysis of single circulating tumor cells by next generation sequencing in metastatic breast cancer
Mutations in the accessory subunit NDUFB10 result in isolated complex I deficiency and illustrate the critical role of intermembrane space import for complex I holoenzyme assembly
Mutation Profiling Indicates High Grade Prostatic Intraepithelial Neoplasia as Distant Precursors of Adjacent Invasive Prostatic Adenocarcinoma
Mutations in proteasome-related genes are associated with thyroid hemiagenesis
Mutation in HFE gene decreases manganese accumulation and oxidative stress in the brain after olfactory manganese exposure
Mutations in spliceosomal proteins and retina degeneration
Mutational mapping of the transmembrane binding site of the G-protein coupled receptor TGR5 and binding mode prediction of TGR5 agonists
Mutations at the Ribosomal S10 Gene in Clinical Strains of Staphylococcus aureus with Reduced Susceptibility to Tigecycline
Mutations of myelodysplastic syndromes (MDS): An update
Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
Mutations in NOTCH1 PEST domain orchestrate CCL19-driven homing of chronic lymphocytic leukemia cells by modulating the tumor suppressor gene DUSP22
Mutation-Structure-Function Relationship Based Integrated Strategy Reveals the Potential Impact of Deleterious Missense Mutations in Autophagy Related Proteins on Hepatocellular Carcinoma (HCC): A Comprehensive Informatics Approach
Mutational profiling in the peripheral blood leukocytes of patients with systemic mast cell activation syndrome using next-generation sequencing
Mutations in the %26quot;Fingers%26apos; subdomain of the deubiquitinase USP1 modulate its function and activity
Mutant Resources and Mutagenomics in crop plants
Mutations in inhibin alpha gene and their association with litter size in Kalahari Red and Nigerian goats
Mutations That Enhance the Ciprofloxacin Resistance of Escherichia coli with qnrA1
Mutation in HvCBP20 (Cap Binding Protein 20) Adapts Barley to Drought Stress at Phenotypic and Transcriptomic Levels
Mutational Profile from Targeted NGS Predicts Survival in LDCT Screening-Detected Lung Cancers
Mutational Analysis of Lassa Virus Glycoprotein Highlights Regions Required for Alpha-Dystroglycan Utilization
Mutational Landscapes of Smoking-Related Cancers in Caucasians and African Americans: Precision Oncology Perspectives at Wake Forest Baptist Comprehensive Cancer Center
Mutations in the JAK/STAT and RAS signaling pathways are common in intestinal T-cell lymphomas
Mutations, evolution and the central role of a self-defined fitness function in the initiation and progression of cancer
Mutation in SLC6A9 encoding a glycine transporter causes a novel form of non-ketotic hyperglycinemia in humans
Mutation in children can cause high risk of hereditary Alzheimer%26apos;s disease
Mutational Hotspot of TET2, IDH1, IDH2, SRSF2, SF3B1, KRAS, and NRAS from Human Systemic Mastocytosis Are Not Conserved in Canine Mast Cell Tumors
Mutated PET117 causes complex IV deficiency and is associated with neurodevelopmental regression and medulla oblongata lesions
Mutations causing mitochondrial disease: What is new and what challenges remain?
Mutation of chromatin modifiers; an emerging hallmark of germinal center B-cell lymphomas
Mutagenic influences of colchicine on phenological and molecular diversity of Calendula officinalis L.
Mutated but Not Deleted Ovine PrPC N-Terminal Polybasic Region Strongly Interferes with Prion Propagation in Transgenic Mice
Mutant uromodulin expression leads to altered homeostasis of the endoplasmic reticulum and activates the unfolded protein response
Mutation Detection in Patients With Advanced Cancer by Universal Sequencing of Cancer-Related Genes in Tumor and Normal DNA vs Guideline-Based Germline Testing
Mutation of Arg191 in FtsZ Impairs Cytokinetic Abscission of Bacillus subtilis Cells
Mutated hybrid inflation on brane and reheating temperature
Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy (vol 47, pg 73, 2015)
Mutant Alpha-Synuclein Causes Age-Dependent Neuropathology in Monkey Brain (vol 35, pg 8345, 2015)
Mutation near the binding interfaces at alpha-hemoglobin stabilizing protein is highly pathogenic
Mutation spectra of histone methyltransferases with canonical SET domains and EZH2-targeted therapy
Mutagenic and genotoxic potential of native air borne particulate matter from industrial area of Rourkela city, Odisha, India
Mutations in LRRK2 impair NF-kappa B pathway in iPSC-derived neurons
Mutational analysis of metastatic lymph nodes from papillary thyroid carcinoma in adult and pediatric patients
Mutation testing for directing upfront targeted therapy and post-progression combination therapy strategies in lung adenocarcinoma
Mutagenic and Cytotoxicity LQB 123 Profile: Safety and Tripanocidal Effect of a Phenyl-t-Butylnitrone Derivative
Mutation: A New Operator in Gravitational Search Algorithm Using Fuzzy Controller
Mutant p53 and ETS2, a Tale of Reciprocity
Mutant IDH: a targetable driver of leukemic phenotypes linking metabolism, epigenetics and transcriptional regulation
Mutational load and mutational patterns in relation to age in head and neck cancer
Mutations in the Human ROBO1 Gene in Pituitary Stalk Interruption Syndrome
Mutation in mitochondrial complex IV subunit COX5A causes pulmonary arterial hypertension, lactic acidemia, and failure to thrive
Mutation Update for COL2A1 Gene Variants Associated with Type II Collagenopathies
Mutational signature of aristolochic acid: Clue to the recognition of a global disease
Mutations in XLF/NHEJ1/Cernunnos gene results in downregulation of telomerase genes expression and telomere shortening
Mutations in human homologue of chicken talpid3 gene (KIAA0586) cause a hybrid ciliopathy with overlapping features of Jeune and Joubert syndromes
Mutation rate at 13 rapidly mutating Y-STR loci in the population of Serbia
Mutation Screening of Her-2, N-ras and Nf1 Genes in Brain Tumor Biopsies
Mutations of NKX2.5 and GATA4 genes in the development of congenital heart disease
Mutations in CIT, encoding citron rho-interacting serine/threonine kinase, cause severe primary microcephaly in humans
Mutational analysis of GALT gene in Greek patients with galactosaemia: identification of two novel mutations and clinical evaluation
Mutations changing tropomodulin affinity for tropomyosin alter neurite formation and extension
Mutant prevention concentration and mutant selection window for 10 antimicrobial agents against Rhodococcus equi
Mutasynthesis of Fluorinated Pactamycin Analogues and Their Antimalarial Activity
Mutations in the Capsid Protein of Brome Mosaic Virus Affecting Encapsidation Eliminate Vesicle Induction In Planta: Implications for Virus Cell-to-Cell Spread
Mutational Analysis of GNAQ and GNA11 to Aid Therapy Management of a Choroidal Melanoma Metastatic to the Contralateral Orbit
Mutating a Conserved Proline Residue within the Trimerization Domain Modifies Na+ Binding to Excitatory Amino Acid Transporters and Associated Conformational Changes
Mutation status of the mediator complex subunit 12 (MED12) in uterine leiomyomas and concurrent/metachronous multifocal peritoneal smooth muscle nodules (leiomyomatosis peritonealis disseminata)
Mutarotation in biologically important pure L-fucose and its enantiomer
Mutations in BCAP31 Cause a Severe X-Linked Phenotype with Deafness, Dystonia, and Central Hypomyelination and Disorganize the Golgi Apparatus
Mutation of FAS, XIAP, and UNC13D Genes in a Patient With a Complex Lymphoproliferative Phenotype
Mutation of RNA Polymerase beta-Subunit Gene Promotes Heterogeneous-to-Homogeneous Conversion of beta-Lactam Resistance in Methicillin-Resistant Staphylococcus aureus
Mutations in cell elongation genes mreB, mrdA and mrdB suppress the shape defect of RodZ-deficient cells
Mutation analysis of the EGFR gene and downstream signalling pathway in histologic samples of malignant pleural mesothelioma
Mutations in the mitochondrial gene C12ORF65 lead to syndromic autosomal recessive intellectual disability and show genotype phenotype correlation
Mutations in TMEM231 cause Meckel-Gruber syndrome
Mutations in the cardiac troponin T gene show various prognoses in Japanese patients with hypertrophic cardiomyopathy
Mutant huntingtin regulates EGF receptor fate in non-neuronal cells lacking wild-type protein
Mutational analysis of genes encoding photosynthetic pigments
Mutations in PTRH2 cause novel infantile-onset multisystem disease with intellectual disability, microcephaly, progressive ataxia, and muscle weakness
Mutant Ras Elevates Dependence on Serum Lipids and Creates a Synthetic Lethality for Rapamycin
Mutational Spectrum of the C1 Inhibitor Gene in a Cohort of Italian Patients with Hereditary Angioedema: Description of Nine Novel Mutations
Mutation Update for UBE3A Variants in Angelman Syndrome
Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly
Mutation of sepJ reduces the intercellular signal range of a hetN-dependent paracrine signal, but not of a patS-dependent signal, in the filamentous cyanobacterium Anabaena sp strain PCC 7120
Mutant cohesin drives chromosomal instability in early colorectal adenomas
Mutarotation in biologically important pure L-fucose and its enantiomer (vol 25, 375101, 2013)
Mutations in the 3c and 7b genes of feline coronavirus in spontaneously affected FIP cats
Mutations of 3c and spike protein genes correlate with the occurrence of feline infectious peritonitis
Mutant prevention concentrations of colistin used in combination with other antimicrobial agents against Acinetobacter baumannii, Klebsiella pneumoniae and Pseudomonas aeruginosa clinical isolates
Mutation in TOR1ALP1 encoding LAP1B in a form of muscular dystrophy: A novel gene related to nuclear envelopathies
Mutational and expressional analysis of ERBB3 gene in common solid cancers
木陶瓷的研究进展
木糖异构化木酮糖的制取及分离纯化
木糖醇的发酵法生产
Mutations in beta-Lactamase AmpC Increase Resistance of Pseudomonas aeruginosa Isolates to Antipseudomonal Cephalosporins
Mutation of Phenylalanine-223 to Leucine Enhances Transformation of Benzo[a]pyrene by Ring-Hydroxylating Dioxygenase of Sphingobium sp FB3 by increasing Accessibility of the Catalytic Site
Mutational screening in patients with profound sensorineural hearing loss and neurodevelopmental delay: Description of a novel m.3861A > C mitochondrial mutation in the MT-ND1 gene
Mutations in PMPCB Encoding the Catalytic Subunit of the Mitochondrial Presequence Protease Cause Neurodegeneration in Early Childhood
Mutation in Rice Abscisic Acid2 Results in Cell Death, Enhanced Disease-Resistance, Altered Seed Dormancy and Development
Mutations in the BAF-Complex Subunit DPF2 Are Associated with Coffin-Siris Syndrome
Mutagenicity, genotoxicity and gene expression of Rad51C, Xiap, P53 and Nrf2 induced by antimalarial extracts of plants collected from the middle Vaupes region, Colombia
Mutations in human AID differentially affect its ability to deaminate cytidine and 5-methylcytidine in ssDNA substrates in vitro
Mutagenic Effects of Ribavirin on Hepatitis E VirusViral Extinction versus Selection of Fitness-Enhancing Mutations
Mutations in Parkinson's Disease-Associated PARK2 Gene Are Accompanied by Imbalance in Programmed Cell Death Systems
Mutations in the promoter, intron and CDS of two FAD2 generate multiple alleles modulating linoleic acid level in yellow mustard
Mutant p53 controls tumor metabolism and metastasis by regulating PGC-1 alpha
Mutation of Asn-475 in the Venezuelan Equine Encephalitis Virus nsP2 Cysteine Protease Leads to a Self-Inhibited State
Mutations in the CDS and promoter of BjuA07.CLV1 cause a multilocular trait in Brassica juncea
Mutation update of transcription factor genes FOXE3, HSF4, MAF, and PITX3 causing cataracts and other developmental ocular defects
Mutation analysis and gene expression profiling of ocular melanomas in cats
Mutant p53 partners in crime
Mutations in PCDH21 cause autosomal recessive cone-rod dystrophy
Mutational Biases and GC-Biased Gene Conversion Affect GC Content in the Plastomes of Dendrobium Genus
Mutations in SELENBP1, encoding a novel human methanethiol oxidase, cause extraoral halitosis
Mutations in THAP1/DYT6 reveal that diverse dystonia genes disrupt similar neuronal pathways and functions
Mutation in ESBL Plasmid from Escherichia coli O104:H4 Leads Autoagglutination and Enhanced Plasmid Dissemination
Mutation-induced spatial differences in neuraminidase structure and sensitivity to neuraminidase inhibitors
Mutational Analysis of a Conserved Glutamate Reveals Unique Mechanistic and Structural Features of the Phosphatase PRL-3
Mutations in SCN3A cause early infantile epileptic encephalopathy
Mutations in the signal transducer and activator of transcription family of genes in cancer
Mutations in PRPS1 causing syndromic or nonsyndromic hearing impairment: intrafamilial phenotypic variation complicates genetic counseling
Mutant-allele fraction heterogeneity is associated with non-small cell lung cancer patient survival
Mutation of the PIK3CA gene as a prognostic factor in patients with colorectal cancer
Mutation at G103 of MtbFtsZ Altered their Sensitivity to Coumarins
Mutations in KRAS codon 12 predict poor survival in Chinese patients with metastatic colorectal cancer
Mutations in Genes Coding for Synaptonemal Complex Proteins and Their Impact on Human Fertility
Mutations in osteoprotegerin account for the CCAL1 locus in calcium pyrophosphate deposition disease
Mutation of mouse p53 Ser23 and the response to DNA damage
Mutations of Residues in Pocket P1 of a Cyclodipeptide Synthase Strongly Increase Product Formation
Mutations in RNA methylating enzymes in disease
Mutations in the plastidic ACCase gene endowing resistance to ACCase-inhibiting herbicide in Phalaris minor populations from India
Mutagenic and genotoxic effects and metal contaminations in fish of the Amambai River, Upper Parana River, Brazil
Mutations in exons 3 and 7 resulting in truncated expression of human ATP6V1B1 gene showing structural variations contributing to poor substrate binding-causative reason for distal renal tubular acidosis with sensorineural deafness
Mutant selection window of four quinolone antibiotics against clinical isolates of Streptococcus pneumoniae, Haemophilus influenzae and Moraxella catarrhalis
Mutating Our Understanding of Brain Tumors and Seizures: Entrez IDH
Mutation status coupled with RNA-sequencing data can efficiently identify important non-significantly mutated genes serving as diagnostic biomarkers of endometrial cancer
Mutations in the P10 region of procaspase-8 lead to chemotherapy resistance in acute myeloid leukemia by impairing procaspase-8 dimerization
Mutant Huntingtin and Elusive Defects in Oxidative Metabolism and Mitochondrial Calcium Handling
Mutations in C-natriuretic peptide (NPPC): a novel cause of autosomal dominant short stature
Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human
Mutant p53 Gains Its Function via c-Myc Activation upon CDK4 Phosphorylation at Serine 249 and Consequent PIN1 Binding
Mutations in the pancreatic secretory enzymes CPA1 and CPB1 are associated with pancreatic cancer
Mutations in BRCA1, BRCA2, and PALB2, and a panel of 50 cancer-associated genes in pancreatic ductal adenocarcinoma
Mutations in the &ITDrosophila&IT homolog of human PLA2G6 give rise to age-dependent loss of psychomotor activity and neurodegeneration
Mutation and Methylation Analysis of Circulating Tumor DNA Can Be Used for Follow-up of Metastatic Colorectal Cancer Patients
Mutant KRAS Circulating Tumor DNA Is an Accurate Tool for Pancreatic Cancer Monitoring
Mutations of candidate tumor suppressor genes at chromosome 3p in intrahepatic cholangiocarcinoma
Mutated hilltop inflation revisited
Mutations in Leptin (LEP) Gene Are Associated with Carcass and Meat Quality Traits in Crossbreed Rabbits
Mutation spectrum of the FZD-4, TSPAN12 AND ZNF408 genes in Indian FEVR patients
Mutations in Homologous Recombination Genes and Outcomes in Ovarian Carcinoma Patients in GOG 218: An NRG Oncology/Gynecologic Oncology Group Study
Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment
Mutant IDH1 Cooperates with ATRX Loss to Drive the Alternative Lengthening of Telomere Phenotype in Glioma
Mutant IDH1 Promotes Glioma Formation In Vivo
Mutation in barley ERA1 (Enhanced Response to ABA1) gene confers better photosynthesis efficiency in response to drought as revealed by transcriptomic and physiological analysis
Mutational profile of primary breast diffuse large B-cell lymphoma
木糖醇醛类化合物对聚乙烯结晶结构及性能的影响
Mutations outside the YMDD motif in the P protein can also cause DHBV resistant to Lamivudine
Mutation analysis of the EGFR gene and its downstream signaling pathway in thymic carcinoma patients from a Chinese Han population
Mutation analysis of 19 commonly used short tandem repeat loci in a Guangdong Han population
Mutation and expression of N233C-D506C of cellulase Cel6B from Thermobifida fusca in Escherichia coli
Mutation on N-terminus of polyhydroxybutyrate synthase of Ralstonia eutropha enhanced PHB accumulation
Mutations within the major hydrophilic region (MHR) of Hepatitis B virus from individuals with simultaneous HBsAg and anti-HBs in Guangzhou, Southern China
Mutations in the chloramphenicol acetyltransferase (S61G, Y105C) increase accumulated amounts and resistance in Pseudomonas aeruginosa
Mutation screening of Chinese Treacher Collins syndrome patients identified novel TCOF1 mutations
Mutations induced by carcinogenic doses of aristolochic acid in kidney of Big Blue transgenic rats
Mutational analysis of IZUMO1R in women with fertilization failure and polyspermy after in vitro fertilization
Mutation spectrum of hyperphenylalaninemia candidate genes and the genotype-phenotype correlation in the Chinese population
Mutational signatures and chromosome alteration profiles of squamous cell carcinomas of the vulva
Mutation and Suppressor Analysis of the Essential Lipopolysaccharide Transport Protein LptA Reveals Strategies To Overcome Severe Outer Membrane Permeability Defects in Escherichia coli
Mutations in COQ8B (ADCK4) found in patients with steroid-resistant nephrotic syndrome alter COQ8B function
Mutation of the HERC 1 Ubiquitin Ligase Impairs Associative Learning in the Lateral Amygdala
Mutations in PI3K110 delta cause impaired natural killer cell function partially rescued by rapamycin treatment
Mutation of the Na+/K+-ATPase Atp1a1a.1 causes QT interval prolongation and bradycardia in zebrafish
Mutant KRAS-driven cancers depend on PTPN11/SHP2 phosphatase
Mutagenic primer-based PCR-RFLP assay for genotyping IRGM gene promoter variant rs4958843 (C/T)
Mutations in bassoon in individuals with familial and sporadic progressive supranuclear palsy-like syndrome
Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2
Mutations in CsPID encoding a Ser/Thr protein kinase are responsible for round leaf shape in cucumber (Cucumis sativus L.)
Mutant p53 stimulates cell invasion through an interaction with Rad21 in human ovarian cancer cells (vol 7, 9076, 2017)
Mutations in INF2 may be associated with renal histology other than focal segmental glomerulosclerosis
Mutations of DnaA-boxes in the oriR region increase replication frequency of the MiniR1-1 plasmid
Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft Palate
Mutational analysis of state-dependent contacts in the pore module of eukaryotic sodium channels
Mutation of friezes
钼钛氧化物的合成表征及性能研究
Mutant KLF1 in Adult Anemic Nan Mice Leads to Profound Transcriptome Changes and Disordered Erythropoiesis
Mutation status and prognostic values of KRAS, NRAS, BRAF and PIK3CA in 353 Chinese colorectal cancer patients
Mutations in TTC21B cause different phenotypes in two childhood cases in China
Mutation accumulation is still potentially problematic, despite declining paternal age: a comment on Arslan et al. (2017)
Mutations in Escherichia coli Polyphosphate Kinase That Lead to Dramatically Increased In Vivo Polyphosphate Levels
Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin
Mutation rates at 42 Y chromosomal short tandem repeats in Chinese Han population in Eastern China
Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss
Mutation spectra and founder effect of TMC1 in patients with non-syndromic deafness in Xiamen area, China
Mutational signatures in oral cancer indicate a complex role for tobacco smoke carcinogens
Mutagenicity and Phthalate Level of Bottled Water Under Different Storage Conditions
Mutations in VP1 and 5 '-UTR affect enterovirus 71 virulence
Mutations in MetG (methionyl-tRNA synthetase) and TrmD [tRNA (guanine-N1)-methyltransferase] conferring meropenem tolerance in Burkholderia thailandensis
Mutation of the Surface Layer Protein SlpB Has Pleiotropic Effects in the Probiotic Propionibacterium freudenreichii CIRM-BIA 129
木糖在甲酸体系中的糠醛转化及控制
Mutant p53-Expressing Cells Undergo Necroptosis via Cell Competition with the Neighboring Normal Epithelial Cells
Mutational Profiling of Non-Small-Cell Lung Cancer Resistant to Osimertinib Using Next-Generation Sequencing in Chinese Patients
Mutations in blind cavefish target the light-regulated circadian clock gene, period 2
Mutations in the genes for keratin-4 and keratin-13 in Swedish patients with white sponge nevus
Mutation load estimation model as a predictor of the response to cancer immunotherapy
Mutations responsible for alcohol tolerance in the mutant of Synechococcus elongatus PCC 7942 (SY1043) obtained by single-cell screening system
Mutation of Torsion Pairs in Triangulated Categories and its Geometric Realization
Mutations in Known and Novel Cancer Susceptibility Genes in Young Patients With Pancreatic Cancer
Mutations in VP1 and 5 '-UTR affect enterovirus 71 virulence (vol 8, 6688, 2018)
Mutability analysis towards 21 STR loci included in the AGCU 21+1 kit in Chinese Han population
Mutations That Alter the Carboxy-Terminal-Propeptide Cleavage Site of the Chains of Type I Procollagen Are Associated With a Unique Osteogenesis Imperfecta Phenotype
Mutations in Caenorhabditis elegans neuroligin-like glit-1, the apoptosis pathway and the calcium chaperone crt-1 increase dopaminergic neurodegeneration after 6-OHDA treatment
Mutant phenotypes for thousands of bacterial genes of unknown function
Mutational and transcriptional landscape of spontaneous gene duplications and deletions in Caenorhabditis elegans
Mutations outside the N-terminal part of RBCK1 may cause polyglucosan body myopathy with immunological dysfunction: expanding the genotype-phenotype spectrum
Mutagenicity, cytotoxic and antioxidant activities of Ricinus communis different parts
Mutational Aberrations Detected in Mucinous Epithelial Ovarian Cancer of Asian Women
Mutational heterogeneity of angioimmunoblastic T-cell lymphoma indicates distinct lymphomagenic pathways
Mutation of the OsSAC1 Gene, which Encodes an Endoplasmic Reticulum Protein with an Unknown Function, Causes Sugar Accumulation in Rice Leaves
Mutational analysis of epidermal and hyperproliferative type I keratins in mild and moderate psoriasis vulgaris patients: a possible role in the pathogenesis of psoriasis along with disease severity
Mutations in L-type amino acid transporter-2 support SLC7A8 as a novel gene involved in age-related hearing loss
Mutational intratumoral heterogeneity of a putative tumor suppressor gene RARRES3 in colorectal cancers
Mutation profiles and clinical characteristics of Chinese males with isolated hypogonadotropic hypogonadism
Mutant Variants of the Substrate-Binding Protein DppA from Escherichia coli Enhance Growth on Nonstandard gamma-Glutamyl Amide-Containing Peptides
Mutational Landscape of DDR2 Gene in Lung Squamous Cell Carcinoma Using Next-generation Sequencing
Mutations in glycyl-tRNA synthetase impair mitochondrial metabolism in neurons
Mutation Analysis in Cultured Cells of Transgenic Rodents
Mutagenesis of an Active-Site Loop in Tryptophan Hydroxylase Dramatically Slows the Formation of an Early Intermediate in Catalysis
Mutations of key driver genes in colorectal cancer progression and metastasis
Mutational spectrum of the CYP1B1 gene in Iranain primary congenital glaucoma family
Mutations in C11orf70 Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry Due to Defects of Outer and Inner Dynein Arms
Mutation responsible for congenital photosensitivity and hyperbilirubinemia in Southdown sheep
Mutational Spectrum Analysis of Seven Genes Associated with Thyroid Dyshormonogenesis
Mutational screening of GABRG2 gene in Pakistani population of Punjab with generalized tonic clonic seizures and children with childhood absence epilepsy
Mutation Analysis of Families with Autosomal Dominant Congenital Cataract: A Recurrent Mutation in the CRYBA1/A3 Gene Causing Congenital Nuclear Cataract
Mutant FGFR3 associated with SADDAN disease causes cytoskeleton disorganization through PLC gamma l/Src-mediated paxillin hyperphosphorylation
Mutations in QRDRs of DNA gyrase and topoisomerase IV genes in nalidixic acid and ciprofloxacin-resistant Salmonella enterica isolated from chicken meat, pork and humans
Mutational Analysis of Oncogenic AKT1 Gene Associated with Breast Cancer Risk in the High Altitude Ecuadorian Mestizo Population
Mutational Analysis of the Bovine Hepacivirus Internal Ribosome Entry Site
Mutant IL-7R alpha and mutant NRas are sufficient to induce murine T cell acute lymphoblastic leukemia
Mutations in algal and cyanobacterial Photosystem I that independently affect the yield of initial charge separation in the two electron transfer cofactor branches
Mutation Detection in Tumor-Derived Cell Free DNA Anticipates Progression in a Patient With Metastatic Colorectal Cancer
Mutagenesis of the FAE1 genes significantly changes fatty acid composition in seeds of Camelina sativa
Mutation of the DNMT3A and IDH1/2 genes in Iranian acute myeloid leukemia patients with normal karyotype (CN-AML): association with other gene mutation and clinical and laboratory characteristics
Mutation hotspots at CTCF binding sites coupled to chromosomal instability in gastrointestinal cancers
Mutation profiles of congenital cataract genes in 21 northern Chinese families
Mutation in fission yeast phosphatidylinositol 4-kinase Pik1 is synthetically lethal with defect in telomere protection protein Pot1
Mutations Conferring Increased Sensitivity to Tripartite Motif 22 Restriction Accumulated Progressively in the Nucleoprotein of Seasonal Influenza A (H1N1) Viruses between 1918 and 2009
Mutation Mechanisms of Human Breast Cancer
Mutant JAK3 phosphoproteomic profiling predicts synergism between JAK3 inhibitors and MEK/BCL2 inhibitors for the treatment of T-cell acute lymphoblastic leukemia
Mutations of the Twik-Related Acid-Sensitive K+ Channel 2 Promoter in Human Primary Aldosteronism
Mutational signatures reveal the role of RAD52 in p53-independent p21-driven genomic instability
Mutations in dock1 disrupt early Schwann cell development
Mutations of the glycine cleavage system genes possibly affect the negative symptoms of schizophrenia through metabolomic profile changes
Mutations in Smad-interacting protein 1 gene are responsible for absence of its expression in Hirschsprung's disease
Mutations in CYB561 Causing a Novel Orthostatic Hypotension Syndrome
Mutations in EEA1 are associated with allergic bronchopulmonary aspergillosis and affect phagocytosis of Aspergillus fumigatus by human macrophages
Mutation and recombination in pathogen evolution: Relevance, methods and controversies
Mutans Streptococci and Dental Caries: A New Statistical Modeling Approach
Mutant monocyte chemoattractant protein-1 protein (7ND) inhibits osteoclast differentiation and reduces oral squamous carcinoma cell bone invasion
Mutations in the pantothenate kinase of Plasmodium falciparum confer diverse sensitivity profiles to antiplasmodial pantothenate analogues
Mutational analysis of substrate specificity in a Citrus paradisi flavonol 3-O-glucosyltransferase
Mutation Screening of the Kruppel-like Factor 1 Gene in Individuals With Increased Fetal Hemoglobin Referred for Hemoglobinopathy Investigation in South of Iran
Mutalisk: a web-based somatic MUTation AnaLyIS toolKit for genomic, transcriptional and epigenomic signatures
Mutations in SZT2 result in early-onset epileptic encephalopathy and leukoencephalopathy
Mutagenic effects of spent potliner and derivatives on Allium cepa L. and Lactuca sativa L.: A molecular approach
Mutations in the mitochondrial ribosomal protein MRPS22 lead to primary ovarian insufficiency
Mutation analysis of the TIA1 gene in Chinese patients with amyotrophic lateral sclerosis and frontotemporal dementia
Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy
Mutational spectrum of the phenylalanine hydroxylase gene in patients with phenylketonuria in the central region of China
Mutation of glucose-6-phosphate dehydrogenase deficiency in Chinese Han children in eastern Fujian
Mutational Pleiotropy and the Strength of Stabilizing Selection Within and Between Functional Modules of Gene Expression
Mutations in the PH Domain of DNM1 are associated with a nonepileptic phenotype characterized by developmental delay and neurobehavioral abnormalities
Mutation and expression of ABCA12 in keratosis pilaris and nevus comedonicus
Mutation screening of the TIA1 gene in Chinese patients with amyotrophic lateral sclerosis/frontotemporal dementia
Mutation of I176R in the E coding region weakens Japanese encephalitis virus neurovirulence, but not its growth rate in BHK-21 cells
Mutations in MICAL-1cause autosomal-dominant lateral temporal epilepsy
Mutations in LRRK2 amplify cell-to-cell protein aggregate propagation: a hypothesis
Mutation allele frequency threshold does not affect prognostic analysis using next-generation sequencing in oral squamous cell carcinoma
Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects
木糖醇生产菌株开发——现状与未来
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations
Mutations in TOP3A Cause a Bloom Syndrome-like Disorder
Mutations in PPCS, Encoding Phosphopantothenoylcysteine Synthetase, Cause Autosomal-Recessive Dilated Cardiomyopathy
Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa
Mutational Analysis of AKT1 and PIK3CA in Intraductal Papillomas of the Breast with Special Reference to Cellular Components
Mutant JAK3 signaling is increased by loss of wild-type JAK3 or by acquisition of secondary JAK3 mutations in T-ALL
Mutations in Sugar-Nucleotide Synthesis Genes Restore Holdfast Polysaccharide Anchoring to Caulobacter crescentus Holdfast Anchor Mutants
Mutations in EMT-Related Genes in ALK Positive Crizotinib Resistant Non-Small Cell Lung Cancers
Mutation in the RRM2 domain of TDP-43 in Amyotrophic Lateral Sclerosis with rapid progression associated with ubiquitin positive aggregates in cultured motor neurons
Mutation of the -RPVR- Propeptide Motif at C-Terminal of the A alpha Chain Is Associated with Decreased Fibrinogen Expression
Mutation update for the GPC3 gene involved in Simpson-Golabi-Behmel syndrome and review of the literature
Mutations in Gene fusA1 as a Novel Mechanism of Aminoglycoside Resistance in Clinical Strains of Pseudomonas aeruginosa
Mutational analysis of ARSB gene in mucopolysaccharidosis type VI: identification of three novel mutations in Iranian patients
母胎界面微环境改变与早产
Mutation induction as a strategy to overcome the restricted genetic base in Physalis
Mutations in the estrogen receptor alpha hormone binding domain promote stem cell phenotype through notch activation in breast cancer cell lines
Mutation of CD2AP and SH3KBP1 Binding Motif in Alphavirus nsP3 Hypervariable Domain Results in Attenuated Virus
Mutations in the Influenza A Virus M1 Protein Enhance Virus Budding To Complement Lethal Mutations in the M2 Cytoplasmic Tail
Mutation Analysis of X-linked Sideroblastic Anemia in a 12-Month-Old Boy by Massively Parallel Sequencing
Mutation screening of the GLIS3 gene in a cohort of 592 Chinese patients with congenital hypothyroidism
Mutations in MARS identified in a specific type of pulmonary alveolar proteinosis alter methionyl-tRNA synthetase activity
Mutations in ppe38 block PE_PGRS secretion and increase virulence of Mycobacterium tuberculosis
Mutations in the COL1A1 and COL1A2 genes associated with osteogenesis imperfecta (OI) types I or III
Mutational analysis of TAF6 revealed the essential requirement of the histone-fold domain and the HEAT repeat domain for transcriptional activation
Mutation in the ADNP gene associated with Noonan syndrome features
Mutational status of NRAS, KRAS, and PTPN11 genes is associated with genetic/cytogenetic features in children with B-precursor acute lymphoblastic leukemia
Mutations in voltage-gated L-type calcium channel: implications in cardiac arrhythmia
Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema
Mutant p53 gain of function underlies high expression levels of colorectal cancer stem cells markers
Mutant p53 cancers reprogram macrophages to tumor supporting macrophages via exosomal miR-1246
Mutant Prevention Concentration and Mutant Selection Window of Micafungin and Anidulafungin in Clinical Candida glabrata Isolates
Mutagenic Analysis of an Adeno-Associated Virus Variant Capable of Simultaneously Promoting Immune Resistance and Robust Gene Delivery
Mutant p53 as a therapeutic target for the treatment of triple-negative breast cancer: Preclinical investigation with the anti-p53 drug, PK11007
Mutations in the U11/U12-65K protein associated with isolated growth hormone deficiency lead to structural destabilization and impaired binding of U12 snRNA
Mutant allele quantification reveals a genetic basis for TP53 mutation-driven castration resistance in prostate cancer cells
Mutational landscape of RNA-binding proteins in human cancers
Mutation in KCNE1 associated to early repolarization syndrome by modulation of slowly activating delayed rectifier K+ current
Mutant MYO1F alters the mitochondrial network and induces tumor proliferation in thyroid cancer
Mutations in Neisseria gonorrhoeae grown in sub-lethal concentrations of monocaprin do not confer resistance
Mutant APP and amyloid beta-induced defective autophagy, mitophagy, mitochondrial structural and functional changes and synaptic damage in hippocampal neurons from Alzheimer's disease
Mutation of Agr Is Associated with the Adaptation of Staphylococcus aureus to the Host during Chronic Osteomyelitis
Mutations in COL1A1 Gene Change Dentin Nanostructure: A Response
Mutations in mevalonate pathway genes in patients with familial or sporadic porokeratosis
Mutational signatures of DNA mismatch repair deficiency in C. elegans and human cancers
Mutations in the gamma-secretase genes PSEN1, PSENEN, and NCSTN in a family with acne inversa
Mutational analysis and dynamic simulation of S-limonene synthase reveal the importance of Y573: Insight into the cyclization mechanism in monoterpene synthases
MutaNET: a tool for automated analysis of genomic mutations in gene regulatory networks
Mutation analysis by whole exome sequencing of endometrial hyperplasia and carcinoma in one patient: Abnormalities of polymerase epsilon and the phosphatidylinositol-3 kinase pathway
Mutation Sensitivity Maps: Identifying Residue Substitutions That Impact Protein Structure Via a Rigidity Analysis In Silico Mutation Approach
Mutations causing low level antibiotic resistance ensure bacterial survival in antibiotic-treated hosts
Mutational screening of inverted formin 2 in adult-onset focal segmental glomerulosclerosis or minimal change patients from the Czech Republic
Mutation of adjacent cysteine residues in the NSs protein of Rift Valley fever virus results in loss of virulence in mice
Mutation Spectrum of the ABCA4 Gene in a Greek Cohort with Stargardt Disease: Identification of Novel Mutations and Evidence of Three Prevalent Mutated Alleles
Mutant Kras Dosage and Chromothripsis: The Right Ingredients for a Pancreatic Cancer Catastrophe
Mutation-linked, excessively tight interaction between the calmodulin binding domain and the C-terminal domain of the cardiac ryanodine receptor as a novel cause of catecholaminergic polymorphic ventricular tachycardia
Mutagenesis Study of the Cytochrome c Subunit Responsible for the Direct Electron Transfer-Type Catalytic Activity of FAD-Dependent Glucose Dehydrogenase
Mutacin 1140 Lantibiotic Variants Are Efficacious Against Clostridium difficile Infection
Mutations in ADNP affect expression and subcellular localization of the protein
Mutation accumulation in populations of varying size: large effect mutations cause most mutational decline in the rotifer Brachionus calyciflorus under UV-C radiation
Mutation analysis of the EBV-lymphoblastoid cell line cautions their use as antigen-presenting cells
Mutational analysis of triple-negative breast cancers within the International Breast Cancer Study Group (IBCSG) Trial 22-00
Mutational analyses of regulatory genes, mexR, nalC, nalD and mexZ of mexAB-oprM and mexXY operons, in efflux pump hyperexpressing multidrug-resistant clinical isolates of Pseudomonas aeruginosa
Mutational analysis on gastric, duodenal, bone, and mediastinal lymph node metastases and blood from a case of primary lung adenocarcinoma
Mutant LRRK2 mediates peripheral and central immune responses leading to neurodegeneration in vivo
Mutation in populations governed by a Galton-Watson branching process
Mutations at multiple CDK phosphorylation consensus sites on Cdt2 increase the affinity of CRL4(Cdt2) for PCNA and its ubiquitination activity in S phase
Mutations in EID1 and LNK2 caused light-conditional clock deceleration during tomato domestication
Mutations in Cytosine-5 tRNA Methyltransferases Impact Mobile Element Expression and Genome Stability at Specific DNA Repeats
Mutations in the Neuroblastoma Amplified Sequence gene in a family affected by Acrofrontofacionasal Dysostosis type 1
Mutant GNAS drives pancreatic tumourigenesis by inducing PKA-mediated SIK suppression and reprogramming lipid metabolism
Mutation-specific effects in germline transmission of pathogenic mtDNA variants
Mutations in Diphosphoinositol-Pentakisphosphate Kinase PPIP5K2 are associated with hearing loss in human and mouse
木炭施用对镉污染土壤小白菜生长及镉吸收的影响
木糖醇月桂酸单酯的分离纯化及其性质表征
Mutations associated with in vitro resistance to bedaquiline in Mycobacterium tuberculosis isolates in Australia
Mutational analysis of candidate genes in Israeli male breast cancer cases
Mutation Study of Malaysian Patients with Ornithine Transcarbamylase Deficiency: Clinical, Molecular, and Bioinformatics Analyses of Two Novel Missense Mutations of the OTC Gene
Mutant huntingtin induces iron overload via up-regulating IRP1 in Huntington's disease
Mutations in BAG3 cause adult-onset Charcot-Marie-Tooth disease
MutatedSocioAgentSim (MSAS): semisupervised modelling of multiagent simulation to predict and detect the mutation in a camouflaged social network
Mutation patterns identify adult patients with de novo acute myeloid leukemia aged 60 years or older who respond favorably to standard chemotherapy: an analysis of Alliance studies
Mutational Profiling of Malignant Mesothelioma Revealed Potential Therapeutic Targets in EGFR and NRAS
Mutations affecting glycinergic neurotransmission in hyperekplexia increase pain sensitivity
Mutation analysis of adenomas and carcinomas of the colon: Early and late drivers
Mutation abundance affects the therapeutic efficacy of EGFR-TKI in patients with advanced lung adenocarcinoma: A retrospective analysis
穆太奈比“国王颂”中的阿拔斯王朝和拜占庭帝国
Mutation of hop-1 and pink-1 attenuates vulnerability of neurotoxicity in C. elegans: the role of mitochondria-associated membrane proteins in Parkinsonism
Mutant Runx2 regulates amelogenesis and osteogenesis through a miR-185-5p-Dlx2 axis
Mutational analysis of KRAS and its clinical implications in cervical cancer patients.
Mutant AFM 2 of Alcaligenes faecalis for phenol biodegradation using He-Ne laser irradiation
木糖接枝改性温度对花生蛋白膜物理性质的影响
Mutation screening of 10 cancer susceptibility genes in unselected breast cancer patients
Mutational Analysis and Allosteric Effects in the HIV-1 Capsid Protein Carboxyl-Terminal Dimerization Domain
木糖醇类成核剂与山梨醇类成核剂对聚丙烯改性性能的比较
母胎依恋关系量表的修订及信效度检验
Mutations in hepatitis B virus polymerase are associated with the postoperative survival of hepatocellular carcinoma patients
Mutational signatures efficiently identify different mutational processes underlying cancers with similar somatic mutation spectra
Mutation spectrum of Chinese patients with Bartter syndrome
Mutational patterns in chemotherapy resistant muscle-invasive bladder cancer
母胎膜早破合并羊膜炎对足月新生儿感染及其并发症的影响
Mutations of deubiquitinase OTUD1 are associated with autoimmune disorders.
Mutations in the tRNA methyltransferase 1 gene TRMT1 cause congenital microcephaly, isolated inferior vermian hypoplasia and cystic leukomalacia in addition to intellectual disability.
Mutation analysis of ZP1, ZP2, ZP3 and ZP4 genes in 152 Han Chinese samples with ovarian endometriosis.
木糖浓度及补料发酵对树干毕赤酵母乙醇发酵的影响
Mutation in IL36RN impairs the processing and regulatory function of the interleukin-36-receptor antagonist and is associated with DITRA syndrome
Mutation in ZFP92 gene is associated with NOA
Mutational profiling of Chinese ROS1 positive non-small cell lung cancer patients with required resistant to crizotinib by next generation sequencing.
Mutation profiling of FGFR genes in solid tumors using comprehensive NGS panel.
MutationalPatterns: comprehensive genome-wide analysis of mutational processes
Mutation profiling and treatment choosing of Chinese ROS1 positive advanced lung cancer patients.
Mutation in the Squalene Epoxidase Gene of Trichophyton interdigitale and Trichophyton rubrum Associated with Allylamine Resistance
Mutations in ATP6AP2 cause autophagic liver disease in humans
Mutant Huntingtin Causes a Selective Decrease in the Expression of Synaptic Vesicle Protein 2C
Mutation of frizzled8a delays neural retinal cell differentiation and results in microphthalmia in zebrafish
Mutation analysis of the TUBB8 gene in primary infertile women with arrest in oocyte maturation
Mutation profiling of cancer and stromal cells from patients with pancreatic ductal adenocarcinoma.
Mutation Analysis of the <b>ATP7B</b> Gene in Seven Chinese Families with Wilson’s Disease
Mutation analysis of 13 RM Y-STR loci in Han population from Beijing of China
Mutation of key amino acids in the polygalacturonase-inhibiting proteins CkPGIP1 and GhPGIP1 improves resistance to Verticillium wilt in cotton
Mutations in RECQL are not associated with breast cancer risk in an Australian population
Mutagenic activity of N -nitrosodiethylamine in cell lines expressing human CYP2E1 - adequacy of dimethylsulfoxide as solvent
Mutant UBQLN2P497H in motor neurons leads to ALS-like phenotypes and defective autophagy in rats
Mutations on Peptidoglycan Synthesis Gene ponA Improve Electro-transformation Efficiency of Corynebacterium glutamicum ATCC 13869
Mutation Status and Immunohistochemical Correlation of KRAS, NRAS, and BRAF in 260 Chinese Colorectal and Gastric Cancers
Mutations of genes including DNMT3A detected by next-generation sequencing in thyroid cancer
Mutations of ARX and non-syndromic intellectual disability in Chinese population
Mutagen-induced phytotoxicity in maize seed germination is dependent on ROS scavenging capacity
Mutations of Mycobacterium tuberculosis induced by anti-tuberculosis treatment result in metabolism changes and elevation of ethambutol resistance
Mutational and cytogenetic analyses of 188 CLL patients with trisomy 12: A retrospective study from the French Innovative Leukemia Organization (FILO) working group
Mutation Analysis of Pre-mRNA Splicing genes in Chinese Families with Autosomal Dominant Retinitis Pigmentosa
Mutation analysis of the ABCC2 gene in Chinese patients with Dubin‑Johnson syndrome
Mutational landscape and clonal diversity of pulmonary adenoid cystic carcinoma
Mutational analysis of dishevelled genes in zebrafish reveals distinct functions in embryonic patterning and gastrulation cell movements
Mutational spectrum and prognostic stratification of intermediate-risk acute myeloid leukemia
Mutant LKB1 Confers Enhanced Radiosensitization in Combination with Trametinib in KRAS-Mutant Non–Small Cell Lung Cancer
Mutational Landscape of Ovarian Adult Granulosa Cell Tumors from Whole Exome and Targeted TERT Promoter Sequencing
Mutation screening of theKIF5Agene in Chinese patients with amyotrophic lateral sclerosis
Mutation of RGG2 , which encodes a type B heterotrimeric G protein γ subunit, increases grain size and yield production in rice
Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond–like syndrome
Mutation analysis at 17 Y-STR loci (Yfiler) in father-son pairs of male pedigrees from Pakistan
Mutation W222L at the Receptor Binding Site of Hemagglutinin Could Facilitate Viral Adaption from Equine Influenza A(H3N8) Virus to Dogs
Mutation screening in Chinese patients with familial Alzheimer's disease by whole-exome sequencing.
Mutagenicity test of magnetic nanocomposite for interface fixation
Mutation Analysis of COL1A1 and COL1A2 in Fetuses with Osteogenesis Imperfecta Type II/III
Mutation tracking in circulating tumor DNA predicts relapse in early breast cancer
Mutations ofNOTCH3in childhood pulmonary arterial hypertension
Mutant hFGF23(A12D) stimulates osteoblast differentiation through FGFR3.
Mutant huntingtin inhibits the mitochondrial unfolded protein response by impairing ABCB10 mRNA stability.
母胎免疫中巨噬细胞作用机制的研究进展
Mutational Effect of Structural Parameters on Coiled-Coil Stability of Proteins
木糖醇和低聚异麦芽糖醇血糖指数的测定
木糖醇石榴汁酸奶发酵工艺研究
木藤蓼化学成分的分离鉴定
Muted change in Atlantic overturning circulation over some glacial-aged Heinrich events
Muted neural response to distress among securely attached people
Mutex Causality in Processes and Traces of General Elementary Nets
Muted, But Not Mute
Muted responses of streamflow and suspended sediment flux in a wildfire-affected watershed
Muted蛋白介导CD63在嗜铬细胞大致密核心颗粒的定位
MuteinDB: the mutein database linking substrates, products and enzymatic reactions directly with genetic variants of enzymes
Muted calcareous nannoplankton response at the Middle/Late Eocene Turnover event in the western North Atlantic Ocean
Muted dental voices on interprofessional healthcare teams
Muthi to medicine
Mutifunctional arc ion plated TiO2 photocatalytic coatings with improved wear and corrosion protection
Mutilins Derivatives: From Veterinary to Human-used Antibiotics
木蹄层孔菌石油醚组分的成分分析及抗肿瘤活性研究
母体血浆中胎儿游离DNA的研究现状及进展
钼铁催化剂的微结构及其对二甲苯选择氧化的催化性能
母体妊娠期和哺乳期蛋白限饲对后代育肥猪肌纤维特性的影响
母体营养不良对子代发育影响研究进展
木蹄层孔菌子实体提取物体外抑菌活性研究
木蹄层孔菌多糖对免疫抑制小鼠免疫功能及细胞因子产生的影响
母体循环中游离胎儿DNA的生物学特点与临产分娩的关系研究
木蹄层孔菌免疫活性多糖超声提取工艺研究
木条演示电介质在静电场中的极化现象
母体学科、知识内核与商务英语专业经管类课程教学——以《国际贸易理论与实务》为例
母体外周血液中胎儿有核红细胞的检测及比例与孕周的关系
母体高校教师在独立学院兼职的工作满意度调查——以湖南农业大学东方科技学院为例
母体水化疗法治疗妊娠晚期羊水过少临床疗效分析
母体铅暴露对仔鼠海马组织中P-tau表达的影响
母体血清学唐氏筛查及产前超声检查对发现三倍体胎儿的价值
母体免疫对斑马鱼亲鱼和胚胎中补体含量及活性的影响
母体血清miR-125b-2直接检测应用于无创产前诊断的相关研究
母体血浆游离HLCS基因用于无创伤性产前诊断DS的研究
母体血浆中白细胞介素11 DNA甲基化和蛋白水平的检测及其临床意义
木蹄层孔菌子实体化学成分及对肿瘤细胞的抑制作用的研究
木蹄层孔菌不同居群间生长特性、木质素降解酶与SRAP标记遗传多样性
母体砷暴露仔鼠肝脑组织中砷形态分布
母体温自身抗体致新生儿溶血病1例报告
母体IFN-γ与IL-1RN基因多态性与早产相关性研究
钼铁桶物料自动运送生产线机械设计技术研究
母体高脂暴露编程子代胰岛素抵抗研究现状
Mutiscale substrates based on hydrogel-incorporated silicon nanowires for protein patterning and microarray-based immunoassays
Mutiple organ damage caused by a novel tick-borne Bunyavirus: A case report
Mutiple three-decision procedure for comparing several exponential treatments with the best control
母体日粮低能量对后代肉仔鸡生长性能、胴体品质和肉质的影响(英文)
母体慢性氟暴露对仔鼠免疫功能的影响
母体氟暴露对仔代胸腺酶组化与超微结构的影响
钼铁冶炼中钼精矿氧化焙烧的工艺分析
钼铁混合金属原子簇的研究Ⅱ(η~5-C_5H_5)_2M_(o2)F_(e2)(μ_3-T_e)_2(μ_3-CO)-(μ_2-CO)(CO)_5的合成及结构
钼铁混合金属原子簇化合物[(η~5-C_5H_5)_4Mo_4Fe_2(μ_3-S)_5(CO)_5]的合成和结构
钼铁硫原子簇化合物的合成与结构化学Ⅲ以Fe(SR)_6为桥的双立方烷化合物的磁学研究
钼铁硫原子簇化合物的合成与结构化学研究 Ⅱ.以Fe(SR)_6为桥的双类立方烷化合物的合成及(Et_4N)_4[Mo_2Fe_7S_8(SC_6H_4CH_3-m)_(12)]·2THF的晶体结构
钼锑抗分光光度法测定海水中活性磷酸盐的浓度
母题、母题位和母题位变体——民间文学叙事基本单位的形式、本质和变形
钼锑抗分光光度法测定可溶性正磷酸盐的不确定度
钼铁硫原子簇化合物的合成与结构化学——Ⅳ.双类立方烷化合物与酰氯的反应
母体对小麦胚的ABA敏感性和种子休眠性的影响
母体亲缘关系在杨氏榕树金小蜂后代性比调节中的作用
钼铁蛋白金属原子簇的拆卸与组装的圆二色谱的研究
母体血浆中Annexin Ⅴ、ET-1、vWF在子痫前期患者中的表达及意义
母体子宫动脉和胎儿脐动脉血流动力学变化对妊娠结局的影响
母体麻醉对胎儿神经发育的影响
母体免疫对斑马鱼胚胎中溶菌酶基因表达的影响
母体妊娠期应激对后代出生前后下丘脑-垂体-肾上腺轴的影响及其机制
母体血清C反应蛋白诊断早发性新生儿败血症的临床价值
木蹄多糖提取工艺研究
母体日粮蛋白水平对仔猪肌细胞生成素基因表达量及初生质量的影响
母体慢性铝暴露对子代鼠海马细胞内Ca~(2+)浓度及记忆行为的影响
母体孕期营养状况对子代后继健康的影响
木条夹根,西瓜坐稳
母题何为——文学母题和母题研究法溯源
木蹄层孔菌乙醇提取物体内抗肿瘤活性及其对荷瘤鼠免疫功能的影响
母体长期服用皮质激素对胎儿脏器的影响—附一例尸检报告
母体心电图中出现的胎儿心电信号1例
木蹄层孔菌培养条件的研究
母体日粮蛋白水平对仔猪抑肌素基因表达量及肌纤维直径的影响
木蹄层孔菌多糖对小鼠免疫功能的影响
钼添加量对硬质合金组织和性能的影响
母体苯胺六聚体的一步法合成及紫外光谱研究
钼铁合金对铜基摩擦材料性能影响
母体铅暴露对仔鼠海马内Calsyntenin-1表达的影响
母体肥胖与子代神经精神疾病相关性及机制的研究进展
母体蛋白质营养对猪肌内脂肪形成的影响研究进展
母体蛋白质水平对雄性后代生殖能力的影响研究
母体环境因素暴露与胎儿先天性心脏病病因关系探讨
木天蓼的“同物异名”及其原植物考证
母体血液循环中胎儿的游离DNA在产前检查中的应用
母题学视角下的朝鲜族英雄神话——以《朱蒙神话》为例
木蹄层孔菌化学成分研究(Ⅱ)
母题学视角下比较“后羿射日”与“阿龙射日月”神话
木蹄层孔菌乙醇提取物对小鼠肝脏和免疫细胞功能的影响
穆铁柱和姚明对中国男篮发展的贡献思考
母体与外界环境影响新生儿肠道微生物区系建立的研究进展
Mutiny on the Boun-T: Controlling Dangerous T Cells Through Anergy
Mutilating Hand Injuries in Children
Mutielemental concentration and physiological responses of Lavandula pedunculata growing in soils developed on different mine wastes
Muti-component nanocomposite of nickel and manganese oxides with enhanced stability and catalytic performance for non-enzymatic glucose sensors
母题视野下的满族英雄故事
母体营养对子代生长发育及代谢的影响研究进展
钼铁冶炼废渣制备水玻璃的试验研究
母体高效价IgG类抗-D抗体致新生儿溶血病相关免疫指标检测及其临床意义
母体超重和肥胖致神经发育障碍炎症机制
母体抗生素应用对新生儿肠道菌群建立的影响
母体血浆细胞纤维结合蛋白不同时期预测妊娠期高血压疾病的价值
母体血清标记物在三体综合征产前诊断中的进展
母体肢体缺血预处理对宫内窘迫胎鼠复氧后海马神经元线粒体结构和功能的影响
钼铁冶炼收尘灰制备钼酸盐的实验研究
木蹄层孔菌化学成分研究
母体高脂饮食编程子代胰岛素抵抗的研究进展
母体暴露壬基酚对仔鼠脾脏组织的氧化损伤
母体营养状况与唇腭裂发生关系的研究
母体铅暴露对仔鼠大脑皮层组织中IL-β1蛋白表达的影响
母体怀孕及哺乳期铅暴露致仔鼠脑海马组织c-fos的变化
母题与主题的联系与区别——以巴尔扎克《高老头》为例
Mutism with abulia for contralateral function: a case of acute left anterior cerebral artery territory stroke
Mutism and Amnesia following High-Voltage Electrical Injury: Psychogenic Symptomatology Triggered by Organic Dysfunction?
Mutiferroic Properties of Polycrystalline Sr-Substituted BiFeO3 Thin Films Prepared by Pulsed Laser Deposition
Mutiny or scrutiny: NK cell modulation of DC function in HIV-1 infection
Mutillidae (Hymenoptera, Aculeata) of the state of Mato Grosso do Sul, Brazil
木蹄复方提取物体内抗肿瘤作用研究
木蹄复方体外抗肿瘤作用的实验研究
木蹄复方水提物对小鼠化学性肝损伤的保护作用研究
母体铅暴露对仔鼠大脑皮层组织中IL-1β和TNF-α表达的影响
母体铅暴露对仔鼠肾脏中MMP-2、MMP-9 mRNA表达的影响
母题的分配、修饰及其与情境的区别——文学母题的重新认识与分类之三
木条与高温铝液作用对铝液中形成氢和氧化铝夹杂的影响研究
木天蓼根茎的化学成分研究
母题·叙事·意象——《行动代号:孙中山》分析
母题制造和框架建构:“宝马撞人案”媒介报道话语分析
母体声音音频在新生儿黄疸蓝光照射治疗中的临床观察
木蹄层孔菌子实体提取物对H22荷瘤小鼠体内抗肿瘤活性的影响
木蹄层孔菌胞外多糖的深层培养工艺优化及体外抗氧化研究
母体血清甲胎蛋白联合超声在产前诊断中的临床应用
母体叶酸水平与子代生长发育状况相关性的研究进展
母体血糖水平对胎儿左心室舒张功能的影响及超声心动图定量分析价值
母体血清PAPP-A、Fβ-hCG联合胎儿NT超声在孕早期胎儿染色体非整倍体异常筛查中的应用价值
Mutifunctional Electrospun Nonwoven Mats with Two-Way Shape Memory Behavior Prepared from Sol-Gel Crosslinked Poly(epsilon-Caprolactone)
母体肢体缺血预处理对宫内窘迫胎鼠复氧后海马神经元凋亡的影响
Mutisiana natural philosophy: Facsimile Edition and study of an unpublished manuscript of Jose Celestino Mutis y Bosio, corresponding to his third inaugural prayer delivered at the Colegio Mayor de Nuestra Senora del Rosario, Santa Fe, October 1764
Mutisiana scientific Medicine: Survey from a medical record footage of Jose Celestino Mutis y Bosio, written in Madrid in 1759 and now preserved in the Archivo Historico Javeriana of Bogota
Mutisiana Academy: pre-New Granadan documents by Jose Celestino Mutis and promotion of scientific societies in New Granada
Mutism and Persistent Dysarthria Due to Tacrolimus-Based Immunosuppression Following Allogeneic Liver Transplantation
Mutiny at the white-hole district
钼铁催化剂对二甲苯气相选择性氧化的研究
母题叙事及其时代演进——以“义犬救主”故事模式的发展演变为例
母体因素导致妊娠晚期胎儿生长受限的预测及新生儿转归
母体血液生物新标志物在唐氏综合征产前诊断效果及对预后的影响研究
钼锑抗分光光度法对黄河表层沉积物中磷的形态分布及其吸附-解吸特征研究
母体血清学指标预测前置胎盘合并胎盘植入研究现状
母体血浆胎儿游离DNA Rh D基因型产前诊断检测
Mutipreconditioned GMRES for simulating stochastic automata networks
母体外周血检测18号染色体三体假阴性1例讨论
Mutiple DICER1-related lesions associated with a germline deep intronic mutation
母体行业发展视域下矿业工程研究生培养
母体铅暴露对仔鼠肝脏MMP-2和MMP-9 mRNA表达的影响
Mutlicolor electroluminescent Si quantum dots embedded in SiOx thin film MOSLED with 2.4% external quantum efficiency
Mutlifocal osseous posttransplantation lymphoproliferative disorder: case report
Mutli-objective H-2 / H-infinity, Optimal Controller Design by Multi-objective Genetic Algorithm for Uncertain Continuous-Time T-S Fuzzy Systems
Mutlifunctional nanoparticles prepared from arginine-modified chitosan and thiolated fucoidan for oral delivery of hydrophobic and hydrophilic drugs
Mutli-Features Prediction of Protein Translational Modification Sites
墓头回提取液对小鼠宫颈癌U14细胞株抑制增殖的实验研究
墓头回的本草考证
木桶理论在项目团队管理中的应用和发展
钼铜的低温导热研究
木通皂苷D在不同pH值和温度下的稳定性
木通皂苷D对CCl_4致小鼠急性肝损伤的保护作用
木桶理论对高校体育教学体系构建的启示
募投项目设计——战略与IPO的双重视角
墓头回提取物作用白血病K562细胞蛋白双向电泳方法的建立
墓头回提取液对荷U14宫颈癌小鼠血清VEGF的影响
墓头回提取液对荷U14宫颈癌小鼠血液流变学的影响
木通属植物化学成分及药理作用研究进展
木桶理论在精神科护理管理中的应用
木通在中药复方中的混用误用及考证辨析
木通科4属植物导管穿孔板的比较研究
木桶原理视角下的体育(与健康)课程领域目标分析
木通皂苷D对Aβ诱导损伤的PC12细胞修复作用
木通基源考证、药用沿革与资源
墓头回木脂素类化学成分及细胞毒活性研究
墓头回环烯醚萜酯提取部位抗肿瘤作用及机制研究
木桶效应在高校图书馆日常工作中的体现
钼桶物料自动转运生产线电控技术研究(英文)
钼铜材料制备技术研究进展
木通的肾毒性析义
木通的临床用药浅析
木通属野生果树的研究进展
木通属植物化学成分及药理活性研究进展
钼铜材料的开发和应用
钼铜铅锌硫化矿脱铅富硫新工艺
木通致急性肾功能衰竭1例
墓头回研究进展
木通属植物木通化学成分及药理活性研究概况
木桶理论在学生管理工作中的解读
木桶原理对高校体育专业理论教学体系构建
木桶理论视角下的大学生职业生涯规划策略
墓头回CO_2超临界萃取物的气相色谱-质谱分析
墓头回挥发油的提取与气相色谱-质谱研究
木通马兜铃的组织培养和快速繁殖
木通马兜铃煎剂对蟾蜍实验性心肌活动的影响
木通提取物对实验性大鼠静脉血栓形成的影响
木通的本草记载及其混乱品种
木通属药用植物研究进展
木通中共有成分木通酸和木通皂苷St_c的检测
木桶效应下“弱县”县域经济竞争力及对策分析——以河北省为例
木桶原理赋予足球运动的启示
木通藤茎中亲水性化学成分的分离与鉴定
木桶理论对班级管理的启示
牧童诗歌发展的农史考察
钼铜混合精矿的浮选分离试验研究
木通属植物种质资源的SRAP分析
墓头回药理活性研究进展
木通——园林中的药食同源植物
木桶原理与反木桶原理在高校学生管理中的应用
木通与川木通及关木通的快速PCR鉴别
木桶原理和反木桶原理在图书馆中的应用——谈馆员整体素质培训和特长培训
木桶原理、反木桶原理与图书馆员培训
牧童归去横牛背,短笛无腔信口吹——从《牧童短笛》看中西田园音画的不同意境
木酮糖激酶基因整合表达载体构建及在酿酒酵母中的过表达
木桶理论的行政法解
钼铜复合材料致密度的影响因素研究
Mutomvo: Mutation testing framework for simulated cloud and HPC environments
木头峪村传统古民居的现状及保护措施
钼铜复合材料研究进展
牧童、可汗、圣主——格斯尔的三功能
木通红喀木虱线粒体基因组的测定与序列分析
钼铜复合粉末的致密化及性能
木通及川木通流通使用情况调查分析
Mutremdamide A and Koshikamides C-H, Peptide Inhibitors of HIV-1 Entry from Different Thennella Species
Muttiarmed tubular selenium with potentially unique electrical properties: Solution-phase synthesis and first-principles calculation
Mutton Traceability Method Based on Internet of Things
Muttalib-Borodin ensembles in random matrix theory - realisations and correlation functions
Muttidetector computed tomographic findings of an unroofed coronary sinus
MutualBoost learning for selecting Gabor features for face recognition
Mutual coupling reduction between large antenna arrays using electromagnetic bandgap (EBG) structures
Mutual information and swap operation in the two-qubit Heisenberg model with Dzyaloshinskii-Moriya anisotropic antisymmetric interaction
Mutual solubility and bulk copolymerization of vinyl monomers with N-substituted maleimide
Mutual coupling suppression in microstrip array using defected ground structure
Mutual coupling suppressing based on a new type electric resonant SRRs in microstrip array
Mutual attraction model for both assortative and disassortative weighted networks
Mutual selection model for weighted networks
Mutually unbiased bases for continuous variables
Mutually assured pathogenicity
Mutually arising abstract and actual
Mutual diffusion dynamics with nonlocal response in SiO2 nanoparticles dispersed PQ-PMMA bulk photopolymer
Mutual projectile and target ionization in 1-MeV/amu N4+ and N5+ + He collisions
Mutual Impedance Between Probes in an Elliptic Waveguide-Part I: Basic Theory
Mutual funds trading strategy based on particle swarm optimization
Mutual Impedance between Probes in an Elliptic Waveguide-Part II: Numerical Results
Mutual-induced fractional Fourier transform in strongly nonlocal nonlinear medium
Mutually independent Hamiltonian cycles in k-ary n-cubes when k is even
Mutual benefits of B-ALL and HLDA/HCDM HLDA 9th Barcelona 2010
Mutual solubilities of selected solvents and 1-(2-hydroxyethyl)-3-methylimidazolium tetrafluoroborate
Mutual solubilities study for binary mixtures of dipropylene glycol dimethyl ether and water via molecular dynamics simulation and AMOEBA polarizable force field
Mutual information and linkage disequilibrium based SNP association study by grouping case-control
Mutual Fluorescence Quenching between Propafenone and Eosin Y and Its Analytical Application
Mutual Fund Governance and Performance: A Quantile Regression Analysis of Morningstar's Stewardship Grade
Mutual injection locking and coherent beam combining of two thulium doped fiber lasers
Mutual compensation of higher-order dispersion in chirped pulse amplification system with regenerative amplifier
Mutual fund herding its impact on stock returns: Evidence from the Taiwan stock market
Mutual influence of a two-carbon hydrocarbyl substituent at silicon and the silatranyl group: Molecular structure of 1-ethyl-, 1-vinyl-, and 1-ethynylsilatranes and their analogues
Mutual enhancement between plasmon and molecular fluorescence of conjugated polymer on metal substrates induced by STM
Mutual information and conditional mean estimation in Poisson channels
Mutual alignment errors due to localized distortion in free-space laser communication links (vol 281, pg 4180, 2008)
Mutual alignment errors due to localized distortion in free-space laser communication links
Mutual injection-locking and coherent combining of two individual fiber lasers
Mutual injection locking of two individual fiber lasers
Mutual information-induced interval selection combined with kernel partial least squares for near-infrared spectral calibration
Mutual injection-locking of two individual double-clad fibre lasers
Mutual influence of two parallel coaxial cracks in a composite material with initial stresses
Mutual impedance of non-parallel conductors with earth return
Mutual injection phase-locking of two double clad fiber lasers
Mutual influence of ammonium hexafluorotitanate and hexafluorosilicate in ammonium fluoride solutions
Mutual Solubilities for Water-o-Nitrotoluene System and Distribution Coefficients for Furfural and Acetic Acid in Water-o-Nitrotoluene System
Mutual Solubility of Alkyl Imidazolium Hexafluorophosphate Ionic Liquids and Water
Mutual Information and Relative Entropy of Sequential Effect Algebras
Mutual interference considered power allocation in OFDM-based cognitive networks: the multiple SUs case
Mutual-Coupling Compensation in Time-Modulated Antenna Arrays for Flat-Top Pattern Synthesis
Mutual interference considered power allocation in OFDM-based cognitive networks: The single SU case
Mutual impedance formula between two arbitrary antenna elements
Mutual RFID Authentication Scheme for Resource-constrained Tags
Mutual Chern-Simons Landau-Ginzburg theory for continuous quantum phase transition of Z(2) topological order
Mutual Information and Boson Radius in a c=1 Critical System in One Dimension
Mutually independent hamiltonian cycles for the pancake graphs and the star graphs
Mutual Rescues between Two Dominant Negative Mutations in Cardiac Troponin I and Cardiac Troponin T
Mutually-antagonistic interactions in baseball networks
Mutual regulation of Crl and Fur in Escherichia coli W3110
Mutual injection locking and coherent combining of three individual fiber lasers
Mutual monitoring in a tradable water rights system: A case study of Zhangye City in Northwest China
Mutual-information-based approach for neural connectivity during self-paced finger lifting task
Mutual information of Pauli channels with correlated noise
Mutual interactions of multiple partially incoherent spatial solitons
Mutual adaptation: Enhancing longer-term sustainability of cross-cultural in-service teacher training initiatives in China
Mutual feedback in e-portfolio assessment: an approach to the netfolio system
Mutual productivity spillovers between foreign and local firms in China
Mutually exclusive T-cell receptor induction and differential susceptibility to human immunodeficiency virus type 1 mutational escape associated with a two-amino-acid difference between HLA class I subtypes
Mutual diffusion coefficients of concentrated 1 : 1 electrolyte from the modified mean spherical approximation
Mutual Chern-Simons gauge theory of spontaneous vortex phase
Mutual interference between serum thyroglobulin and antithyroglobulin antibody in an automated chemiluminescent immunoassay
Mutual Chern-Simons theory for Z(2) topological order
Mutual information-based multimodal image registration using a novel joint histogram estimation
Mutual enhancement of central neurotoxicity induced by ketamine followed by methamphetamine
Mutual alignment errors analysis based on wavelet due to antenna deformations in inter-satellite laser communications
Mutual Fund Family Size and Mutual Fund Performance: The Role of Regulatory Changes
Mutual cancellation between tones presented by air conduction, by bone conduction and by non-osseous (soft tissue) bone conduction
Mutual-reinforcement document summarization using embedded graph based sentence clustering for storytelling
Mutual regulation between microRNA-373 and methyl-CpG-binding domain protein 2 in hilar cholangiocarcinoma
Mutually exclusive redox forms of HMGB1 promote cell recruitment or proinflammatory cytokine release
Mutually independent Hamiltonian cycles in alternating group graphs
Mutual Coupling Reduction of Two PIFAs With a T-Shape Slot Impedance Transformer for MIMO Mobile Terminals
Mutualistic association of Paecilomyces formosus LHL10 offers thermotolerance to Cucumis sativus
Mutual compatibility of AlGaN HEMT and HTS (YBCO) technology
Mutual Information Analysis Reveals Coevolving Residues in Tat That Compensate for Two Distinct Functions in HIV-1 Gene Expression
Mutually inductive interactions between the lens and retina require ALK3 functions during mouse embryonic development
Mutual Solid Solubility and Phase Equilibrium in the System BaTiO3-BaCeO3
Mutually beneficial doping of tellurium and nitrogen in ZnO films grown by metal-organic chemical vapor deposition
Mutual Synchronization of Multiple Robot Manipulators with Unknown Dynamics
Mutually Complementary Metal- and Organocatalysis with Collective Synthesis: Asymmetric Conjugate Addition of 1,3-Carbonyl Compounds to Nitroenynes and Further Reactions of the Products
Mutual interaction between a superconducting vortex and a magnetic vortex: A numerical simulation study
Mutually enhanced near infrared emission of Dy3+ and Tm3+ codoped chalcohalide glasses
Mutually exclusive regulation of T cell survival by IL-7R and antigen receptor-induced signals
Mutual Regioselective Inhibition of Human UGT1A1-Mediated Glucuronidation of Four Flavonoids
Mutual Influences of Intermodal Visual/Tactile Apparent Motion and Auditory Motion with Uncrossed and Crossed Arms
Mutual Inductance Measurement of the Superconducting Coil for the Joule Balance
Mutual Capacitive Flexible Tactile Sensor for 3-D Image Control
Mutual diffusion in the ternary mixture of water plus methanol plus ethanol and its binary subsystems
Mutual effect of subcutaneously transplanted human adipose-derived stem cells and pancreatic islets within fibrin gel
Mutually permutable products and conjugacy classes
Mutual access authentication in wireless wearable networks based on trusted platform module
Mutual fund product selection model: An application of the method for ranking interval number
Mutual localization of mobile robots using an omni-vision system
Mutual authentication protocol for mobile RFID systems
母兔超数排卵影响因素的研究
Mutual interference research for pica-satellite TT&C transponder
Mutual Coupling Calibration for Microstrip Antenna Arrays via Element Pattern Reconstruction Method
Mutual information evaluation: A way to predict the performance of feature weighting on clustering
Mutual interaction between YAP and c-Myc is critical for carcinogenesis in liver cancer
Mutual HIV Disclosure among HIV-Negative Men Who have Sex with Men in Beijing, China, 2010
Mutual Interaction Between YAP and CREB Promotes Tumorigenesis in Liver Cancer
Mutually opposing forces during locomotion can eliminate the tradeoff between maneuverability and stability
Mutual dualities between A(-infinity)(Omega) and A(infinity)((Omega)over-tilde) for lineally convex domains
Mutually exclusive binding of APPL(PH) to BAR domain and Reptin regulates beta-catenin dependent transcriptional events
Mutual promotion mechanism for adsorption of coexisting Cr(III) and Cr(VI) onto titanate nanotubes
Mutual Information Criterion-Based Optimal Scale Selection for Image Denoising and Segmentation
Mutual Defense Scheme for Secure Data Aggregation in Wireless Sensor Networks
Mutual action of optical activity effect and linear electro-optic effect in periodically poled "gyroelectric" crystal
Mutual influence between covalent and noncovalent interactions in H3N-MCN-XF (X = H, Li, Cl, Br; M = Ag, Cu, Au)
Mutual Distance Bounding Protocol with Its Implementability Over a Noisy Channel and Its Utilization for Key Agreement in Peer-to-Peer Wireless Networks
Mutual Coupling in Antenna Arrays 2013
Mutual mate choice in the Asiatic toad, Bufo gargarizans, exerts stabilizing selection on body size
Mutual inclusion in a nonlocal competitive Lotka Volterra system
Mutual inhibition between YAP and SRSF1 maintains long non-coding RNA, Malat1-induced tumourigenesis in liver cancer
Mutual impacts of wheat (Triticum aestivum L.) and earthworms (Eisenia fetida) on the bioavailability of perfluoroalkyl substances (PFASs) in soil
Mutual ionization in atomic collisions near the electronic threshold
Mutual transformations between the P-Q, Q-P, and generalized Weyl ordering of operators
Mutual verification of two new quantum simulation approaches for nanomagnets
Mutual coupling calibration and remedy method for polarization sensitive sensors
Mutualism and manipulation in Hadza-honeyguide interactions
Mutual engagement and collocation with shared representations
Mutual Funds and Information Diffusion: The Role of Country-Level Governance
Mutual awareness in collaborative design: An Augmented Reality integrated telepresence system
Mutual Abrasion of Endocardial Leads: Analysis of Explanted Leads
Mutual rectification of alternating currents in graphene in the field of two electromagnetic waves
Mutual powerlessness in client participation practices in mental health care
Mutual information-based binarisation of multiple images of an object: an application in medical imaging
Mutually unbiased measurements in finite dimensions
Mutual information-based method for selecting informative feature sets
Mutual information and the fidelity of response of gene regulatory models
Mutualisms between ants (Hymenoptera: Formicidae) and honeydew-producing insects: Are they important in ant invasions?
Mutual-friend based attacks in social network systems
Mutual Authenticate Protocol Among Sensors in the Military Operation Environment
Mutual modulation between norepinephrine and nitric oxide in haemocytes during the mollusc immune response
Mutually tangled colloidal knots and induced defect loops in nematic fields
Mutual grooming among adult male chimpanzees: the immediate investment hypothesis
Mutually orthogonal Latin squares based on general linear groups
Mutually unbiased bases and bound entanglement
Mutual Conversion between Stretched and Contracted Helices Accompanied by a Drastic Change in Color and Spatial Structure of Poly(phenylacetylene) Prepared with a [Rh(nbd)Cl](2)-Amine Catalyst
Mutualism fails when climate response differs between interacting species
Mutualism vs. antagonism in introduced and native ranges: Can seed dispersal and predation determine Acacia invasion success?
Mutual regulation between Hippo signaling and actin cytoskeleton
Mutual protection against UV aging of EVA composites using highly active optical conversion additives
Mutual binding of polymer end-groups by complementary pi-pi-stacking: a molecular %26quot;Roman Handshake%26quot;
Mutual influence of parallel, CH/O, OH/pi and lone pair/pi interactions in water/benzene/water system
Mutualism between armoured scale insects and ants: new species and observations on a unique trophobiosis (Hemiptera: Diaspididae; Hymenoptera: Formicidae: Melissotarsus Emery)
Mutual information as a measure of image quality for 3D dynamic lung imaging with EIT
Mutualistic interaction between Salmonella enterica and Aspergillus niger and its effects on Zea mays colonization
Mutualistic Co-evolution of Type III Effector Genes in Sinorhizobium fredii and Bradyrhizobium japonicum
Mutually unbiased probability-operator measurements
Mutual expression of the transcription factors Runx3 and ThPOK regulates intestinal CD4(+) T cell immunity
Mutual inhibition through hybrid oligomer formation of daptomycin and the semisynthetic lipopeptide antibiotic CB-182,462
Mutually describing multisets and integer partitions
Mutual Information Analysis of OFDM Radio Link Under Phase Noise, IQ Imbalance and Frequency-Selective Fading Channel
Mutual neutralization in H+-H- collisions by electron capture
Mutualistic Mimicry and Filtering by Altitude Shape the Structure of Andean Butterfly Communities
Mutual Coupling Reduction and Gain Enhancement Using Angular Offset Elements in Circularly Polarized Patch Array
Mutual Information Matrices Are Not Always Positive Semidefinite
Mutual Pulling Between Two Oscillators
Mutual Agreement Between Providers in Intensive Care Medicine on Patient Care After Interdisciplinary Rounds
Mutual interferometric characterization of a pair of independent electric fields
Mutual inductance instability of the tip vortices behind a wind turbine
Mutual selection in time-varying networks
Mutual influence of cetyltrimethylammonium bromide and Triton X-100 on their adsorption at the water-air interface
Mutual Effects of Rottboellia cochinchinensis and Maize Grown Together at Different Densities
Mutual diffusion dynamics as matter transfer mechanism in inorganic nanoparticles dispersed photopolymer
Mutual influence of the velocity and temperature in the axisymmetric FE model of a disc brake
Mutual solubilities of water and hydrocarbons from the Cubic plus Association equation of state: A new mixing rule for the correlation of observed minimum hydrocarbon solubilities
Mutually synchronized bottom-up multi-nanocontact spin-torque oscillators
Mutual Information between Discrete and Continuous Data Sets
Mutual Redundancies in Interhuman Communication Systems: Steps Toward a Calculus of Processing Meaning
Mutual antagonism between hypoxia-inducible factors 1 alpha and 2 alpha regulates oxygen sensing and cardio-respiratory homeostasis
Mutual Antagonism between Circadian Protein Period 2 and Hepatitis C Virus Replication in Hepatocytes
Mutually unbiased projectors and duality between lines and bases in finite quantum systems
Mutual Use of Trail-Following Chemical Cues by a Termite Host and Its Inquiline
Mutual diffusion coefficients in systems containing the nickel ion
Mutual antagonism between Sox10 and NFIA regulates diversification of glial lineages and glioma subtypes
Mutual diffusion coefficients, density, and viscosity of aqueous solutions of new polyamine CO2 absorbents
Mutualism and asexual reproduction influence recognition genes in a fungal symbiont
Mutualism between autotrophic ammonia-oxidizing bacteria (AOB) and heterotrophs present in an ammonia-oxidizing colony
Mutual diffusion coefficients of L-glutamic acid and monosodium L-glutamate in aqueous solutions at T=298.15 K
Mutual diffusion coefficients of L-lysine in aqueous solutions
Mutually Aware Prefetcher and On-Chip Network Designs for Multi-Cores
Mutual Induced Fit in a Synthetic Host-Guest System
Mutual Attractions of Partially Immersed Parallel Plates
Mutual information between thermo-field doubles and disconnected holographic boundaries
Mutual interactions between carbonation and titanium dioxide photoactivity in concrete
Mutual Influence Between Adhesion and Molecular Conformation: Molecular Geometry is a Key Issue in Interphase Formation
Mutual Enlightenment
Mutual information in Hawking radiation
Mutual coupling of antennas in a meteor radar interferometer
Mutual inductance calculation between arbitrarily positioned rectangular filaments
Mutually beneficial host exploitation and ultra-biased sex ratios in quasisocial parasitoids
Mutually disjoint t-designs and t-SEEDs from extremal doubly-even self-dual codes
Mutual interaction of N, B, and O during heteroepitaxial diamond growth: Triggering the nitrogen induced growth acceleration
Mutually exclusive mutations of KIT and RAS are associated with KIT mRNA expression and chromosomal instability in primary intracranial pure germinomas
Mutualistic interaction of rhizobacteria with arbuscular mycorrhizal fungi and its antagonistic effect on Fusarium oxysporum in Carica papaya seedlings
Mutual mode control of short- and long-range surface plasmons
Mutually beneficial relationship in optimization between search-space smoothing and stochastic search
Mutual conversion and asymmetric transmission of linearly polarized light in bilayered chiral metamaterial
Mutually unbiased triplets from non-affine families of complex Hadamard matrices in dimension 6
Mutual diffusion of sodium hyaluranate in aqueous solutions
Mutual Separation of Gallium, Indium and Zinc Using Silica Gel Modified by a Surfactant Micelle Containing D2EHPA
Mutual Exclusivity Analysis of Genetic and Epigenetic Drivers in Melanoma Identifies a Link Between p14(ARF) and RAR beta Signaling
Mutual information-based feature selection for multilabel classification
Mutualistic Networks (MPB-53)
Mutual interaction of kisspeptin, estrogen and bone morphogenetic protein-4 activity in GnRH regulation by GT1-7 cells
Mutual localization in multi-robot systems using anonymous relative measurements
Mutualistic ants as an indirect defence against leaf pathogens
Mutual amplification of corticosteroids and angiotensin systems in human vascular smooth muscle cells and carotid atheroma
Mutual Distance Bounding Protocols
Mutual spectral residual approach for multifocus image fusion
Mutually exclusive FGFR2, HER2, and KRAS gene amplifications in gastric cancer revealed by multicolour FISH
Mutually unbiased measurements for high-dimensional time-bin-based photonic states
Mutual interplay of non-covalent interactions in modulating the geometry of organic linkers in their salts
Mutual Cross Talk between the Regulators Hac1 of the Unfolded Protein Response and Gcn4 of the General Amino Acid Control of Saccharomyces cerevisiae
Mutual Lewis Acid-Base Interactions of Cations and Anions in Ionic Liquids
Mutual evaluation of global gravity models (EGM2008 and GOCE) and terrestrial data in Amazon Basin, Brazil
Mutual influence of openings on strength of shell-type structures under plastic deformation
Mutual replacement of species in space in a grassland community: is there an evidence for functional complementarity of replacement groups?
Mutual effects between aromatic amino acids and guanosine upon vitamin B2 photosensitization in the presence of visible light
Mutual Coupling Reduction between Closely-Placed MSAs for Bi-Static Radar Using Wave Absorber
Mutual Regulation between Raf/MEK/ERK Signaling and Y-Box-Binding Protein-1 Promotes Prostate Cancer Progression
Mutual regulation of TGF-beta 1, T beta RII and ErbB receptors expression in human thyroid carcinomas
Mutual interactions of oscillating quartz tuning forks in superfluid He-4
Mutual information concept for evaluation of separation quality in hyphenated chromatographic measurements
Mutually Independent Hamiltonian Cycles in Some Graphs
Mutual influence of light and CO2 on carbon sequestration via cultivating mixotrophic alga Auxenochlorella protothecoides UMN280 in an organic carbon-rich wastewater
Mutual authentication protocol for electricity consumption information acquisition system
Mutual information optimization based dynamic log-polar image registration
Mutual Information-Assisted Wavelet Function Selection for Enhanced Rolling Bearing Fault Diagnosis
Mutual compensation property of electrooptic and magnetooptic effects and its application to sensor
Mutually modulated cross-gain modulation with a considerable modulation wavenumber-interaction length product
Mutual Information Analysis on Spatial Modulation Multiple Antenna System
Mutual-Information-Based Semi-Supervised Hyperspectral Band Selection With High Discrimination, High Information, and Low Redundancy
Mutually unbiased maximally entangled bases in C-d circle times C-kd
Mutual coupling efficient analysis of rectangle microstrip circular polarization antenna array
Mutual interferences of driving and texting performance
Mutual coupling calibration for L-shaped microstrip antenna array with accurate 2-D direction of arrival estimation
Mutual Antagonism of Wilms' Tumor 1 and beta-Catenin Dictates Podocyte Health and Disease
Mutual Inhibition between Catalytic Impurities of Sulfur and Those of Calcium in Coke during Carbon-Air and Carbon-CO2 Reactions
Mutually Unbiasedness between Maximally Entangled Bases and Unextendible Maximally Entangled Systems in
Mutual exclusion role constraint mining based on weight in role-based access control system
Mutual optical format conversion between on-of keying and binary phase-shift keying based on stimulated brillouin scattering
Mutual solubilities of terpene in methanol and water and their multicomponent liquid-liquid equilibria
Mutual coupling in longitudinal arrays of compound slots
Mutual invadability near evolutionarily singular strategies for multivariate traits, with special reference to the strongly convergence stable case
Mutual effect of vibrational relaxation and chemical reactions in viscous multitemperature flows
Mutually beneficial pollinator diversity and crop yield outcomes in small and large farms
Mutual Coupling Suppression Between Two Closely Spaced Microstrip Antennas With an Asymmetrical Coplanar Strip Wall
Mutually unbiased product bases for multiple qudits
Mutual distance dependence drives the observed jet-power-radio-luminosity scaling relations in radio galaxies
Mutual interaction between guest drug molecules and host nanoporous silica xerogel studied using central composite design
Mutual Authentication Scheme in Secure Internet of Things Technology for Comfortable Lifestyle
Mutual diffusion behavior of short chain alcohols plus n-octane mixtures
Mutual Wattle Ornaments in the South Island Saddleback (Philesturnus carunculatus) Function as Armaments
Mutual Solubility of Water and Hydrocarbons
Mutual sensitization mechanism and self-degradation property of drug delivery system for in vitro photodynamic therapy
Mutual Regulation of Epicardial Adipose Tissue and Myocardial Redox State by PPAR-gamma/Adiponectin Signalling
Mutual Coupling Reduction for UWB MIMO Antennas With a Wideband Neutralization Line
Mutual influence of the sliding velocity and temperature in frictional heating of the thermally nonlinear disc brake
Mutual diffusion coefficients of isopropanol plus n-heptane and isobutanol plus n-heptane
Mutually repressive interaction between Brn1/2 and Rorb contributes to the establishment of neocortical layer 2/3 and layer 4
Mutualism (carpooling) of ecologists and taxonomists
Mutual facilitations of food waste treatment, microbial fuel cell bioelectricity generation and Chlorella vulgaris lipid production
Mutual diffusion of binary liquid mixtures containing methanol, ethanol, acetone, benzene, cyclohexane, toluene, and carbon tetrachloride
Mutual co-influence of natural and socio-humanitarian sciences on social processes
Mutually orthogonal rectangular gerechte designs
Mutual Information, Fisher Information, and Efficient Coding
Mutual information and spontaneous symmetry breaking
Mutually exclusive BCOR internal tandem duplications and YWHAE-NUTM2 fusions in clear cell sarcoma of kidney: not the full story
Mutually enhancing anti-inflammatory activities of dimethyl fumarate and NF-B inhibitors - implications for dose-sparing combination therapies
Mutually-Reactive, Fluorogenic Hydrocyanine/Quinone Reporter Pairs for In-Solution Biosensing via Nanodroplet Association
Mutual Authentication and Updating the Authentication Key in MANETS
Mutual medication in capuchin monkeys-Social anointing improves coverage of topically applied anti-parasite medicines
Mutual interaction of dog sperm LDHC4, PH-20, actin and tubulin proteins and their immunocontraceptive potential in bitches
Mutual interaction between iron homeostasis and obesity pathogenesis
Mutual exclusion by four shared bits with not more than quadratic complexity
Mutual Effect of Plasma Oxygen and Oxidative Degradation of a Polyethylene Film
Mutual effects of pyrite and moisture on coal self-heating rates and reaction rate data for pyrite oxidation
Mutual Information Analysis of Sleep EEG in Detecting Psycho-Physiological Insomnia
Mutual Verifiable Provable Data Auditing in Public Cloud Storage
Mutual Effects of Boron and Zinc on Peanut (Arachis hypogaea L.) Growth and Mineral Nutrition
Mutual influence between contiguous TMPyP4 ligands when bound to a synthetic double-stranded Poly(A)-Poly(U)
Mutual Coupling Compensation Matrices for Transmitting and Receiving Arrays
Mutual associations between patients' and partners' depression and quality of life with respect to relationship quality, physical complaints, and sense of coherence in couples coping with cancer
Mutual induction of transcription factor PPAR gamma and microRNAs miR-145 and miR-329
Mutual Synchronization for Power Generation and Beam-Steering in CMOS With On-Chip Sense Antennas Near 200 GHz
Mutual information reveals multiple structural relaxation mechanisms in a model glass former
Mutual enhancement of IL-2 and IL-7 on DNA vaccine immunogenicity mainly involves regulations on their receptor expression and receptor-expressing lymphocyte generation
Mutual Solubilities for the Water-2-sec-Butylphenol System and Partition Coefficients for Furfural and Formic Acid in the Water-2-sec-Butylphenol System
Mutual coupling reduction of dual port antenna using zero index metasurface structure
Mutual information and the F-theorem
Mutual information on the fuzzy sphere
Mutual antagonism of the paired-type homeobox genes, vsx2 and dmbx1, regulates retinal progenitor cell cycle exit upstream of ccnd1 expression
Mutual gains or mutual losses? Organisational fragmentation and employment relations outcomes at Qantas Group
Mutually orthogonal latin squares with large holes
Mutually unbiased bases with free parameters
Mutual Interactions of CO2/Oil and Natural Gas/Oil Systems and Their Effects on the EOR Process
Mutual Cross-Feeding Interactions between Bifidobacterium longum subsp longum NCC2705 and Eubacterium rectale ATCC 33656 Explain the Bifidogenic and Butyrogenic Effects of Arabinoxylan Oligosaccharides
Mutual dependency of features in multimodal biometric systems
Mutually unbiased Bush-type Hadamard matrices and association schemes
Mutually unbiased weighing matrices
Mutual relation among lattice distortion, Hall effect property and band edge cathodoluminescence of heavily-boron-doped microwave-plasma CVD diamond films homoepitaxially grown on vicinal (001) high-pressure/high-temperature-synthesized Ib substrates
Mutually Disjoint 5-Designs and 5-Spontaneous Emission Error Designs from Extremal Ternary Self-Dual Codes
Mutual constraint using partial occlusion artifact removal for computational integral imaging reconstruction
Mutual and asynchronous anticipation and action in sports as globally competitive and locally coordinative dynamics
Mutual Influence of a Deeply Buried Grounding Electrode and the Surrounding Grounding Mesh
Mutual interaction of basophils and T cells in chronic inflammatory diseases
Mutual Information Analysis for Three-Phase Dynamic Current Mode Logic against Side-Channel Attack
Mutual Information-based multi-label feature selection using interaction information
Mutually converted arc-line segment-based SLAM with summing parameters
Mutual Information between Discrete Variables with Many Categories using Recursive Adaptive Partitioning
Mutualistic fungal endophytes produce phytohormones and organic acids that promote japonica rice plant growth under prolonged heat stress
Mutual Independence of Critical Temperature and Superfluid Density under Pressure in Optimally Electron-Doped Superconducting LaFeAsO1-xFx
Mutual Exacerbation of Peroxisome Proliferator-Activated Receptor gamma Coactivator 1 alpha Deregulation and alpha-Synuclein Oligomerization
Mutual associations among musculoskeletal diseases and metabolic syndrome components: A 3-year follow-up of the ROAD study
Mutual interference in Dolichogenidea tasmanica (Cameron) (Hymenoptera: Braconidae) when foraging for patchily-distributed light brown apple moth
Mutual inclusion in asynchronous message-passing distributed systems
Mutual upregulation of endothelin-1 and IL-25 in atopic dermatitis
Mutual Scorn Within the Abortion Debate: Some Parallels With Race Relations
Mutual stabilisation between (M4L6)-L-II tetrahedra and (MX42-)-X-II metallate guests
Mutual information criterion for feature selection from incomplete data
Mutualism-disrupting allelopathic invader drives carbon stress and vital rate decline in a forest perennial herb
Mutual relationship between anxiety and pain in the intensive care unit and its effect on medications
Mutualism-parasitism paradigm synthesized from results of root-endophyte models
Mutualistic and antagonistic trophic interactions in canola: The role of aphids in shaping pest and predator populations
Mutually connected component of networks of networks with replica nodes
Mutualism Between Fire Ants and Mealybugs Reduces Lady Beetle Predation
Mutual neutralization in collisions of Li+ and F-
Mutually beneficial and sustainable management of Ethiopian and Egyptian dams in the Nile Basin
Mutualistic relationships under landscape change: Carnivorous mammals and plants after 30 years of land abandonment
Mutual and Self-Diffusivities in Binary Mixtures of [EMIM][B(CN)(4)] with Dissolved Gases by Using Dynamic Light Scattering and Molecular Dynamics Simulations
Mutual perception of communication between general practitioners and hospital-based specialists
Mutual information as an order parameter for quantum synchronization
Mutually interacting tachyon dark energy with variable G and Lambda
Mutually temporally independent connectivity patterns: A new framework to study the dynamics of brain connectivity at rest with application to explain group difference based on gender
Mutual vibrational quenching in CO + H-2 collisions
Mutual information-based LPI optimisation for radar network
Mutually Exclusive Roles of SHARPIN in Integrin Inactivation and NF-kappa B Signaling
Mutual effects of melatonin and activin on induction of aldosterone production by human adrenocortical cells
Mutuality in the provision of Scottish healthcare
Mutually Coordinated Visualization of Product and Supply Chain Metadata for Sustainable Design
Mutually Exclusive Formation of G-Quadruplex and i-Motif Is a General Phenomenon Governed by Steric Hindrance in Duplex DNA
Mutualisms in a changing world: an evolutionary perspective
Mutual Conversion of Three Flavors of Gaussian Type Orbitals (vol 90, pg 227, 2002)
Mutual Capture of Dipolar Molecules at Low and Very Low Energies. I. Approximate Analytical Treatment
Mutual doping of components in magnetoelectric particulate PbZr(0.53)Ti(0.47)O(3)-Mn(0.4)Zn(0.6)Fe(2)O(4) composite
Mutual transformation of polarizations on an isolated level in weak electric and magnetic fields
Mutual stabilization of components in composites of polyoxomolybdates of buckyball structure and water-soluble nonionic polymers
Mutualisms with the wreckage of an avifauna: the status of bird pollination and fruit-dispersal in New Zealand
Mutually unbiased bases and complementary spin 1 observables
Mutual Mate Choice for Colorful Traits in King Penguins
Mutually Aposyndetic Decomposition of Homogeneous Continua
Mutually independent bipanconnected property of hypercube
Mutual Interplay of Light Harvesting and Triplet Sensitizing in a Perylene Bisimide Antenna-Fullerene Dyad
Mutual Inductance Calculation Between Circular Filaments Arbitrarily Positioned in Space: Alternative to Grover's Formula
Mutual Antagonism Between the Anaphase Promoting Complex and the Spindle Assembly Checkpoint Contributes to Mitotic Timing in Caenorhabditis elegans
Mutual Slowing-Down Effects in Mixture Diffusion in Zeolites
Mutual regulation of cyclin-dependent kinase and the mitotic exit network
Mutual coupling of two semiconductor quantum dots via an optical nanocavity
Mutual information is critically dependent on prior assumptions: would the correct estimate of mutual information please identify itself?
Mutual Coupling Reduction Between Microstrip Patch Antennas Using Slotted-Complementary Split-Ring Resonators
Mutual mate choice by mountain pine beetles: size-dependence but not size-assortative mating
Mutually orthogonal Latin squares and mutually unbiased bases in dimensions of odd prime power MOLS and MUBs in odd prime power dimensions
Mutual Coupling in Antenna Arrays
Mutually orthogonal Latin squares from the inner products of vectors in mutually unbiased bases
Mutual understanding in multi-disciplinary primary health care teams
Mutualistic mycorrhiza-like symbiosis in the most ancient group of land plants
Mutual diffusion with equal eigenvalues in solutions of strongly associated surfactants. A new kind of multicomponent diffusion
Mutualism variation in the nodulation response to nitrate
Mutual coherence of laser solitons in coupled semiconductor resonators
Mutualism favours higher host specificity than does antagonism in plant-herbivore interaction
Mutual interference problems in the simultaneous voltammetric determination of trace total mercury(II) in presence of copper(II) at gold electrode. Applications to environmental matrices
Mutual-Information-Based Registration of TerraSAR-X and Ikonos Imagery in Urban Areas
Mutual Information Statistics and Beamforming Performance Analysis of Optimized LoS MIMO Systems
Mutually Disjoint Designs and New 5-Designs Derived from Groups and Codes
Mutual Solubility of Pyridinium-Based Tetrafluoroborates and Toluene
Mutual Solubility Study in Supercritical Fluid Extraction of Tocopherols from Crude Palm Oil Using CO2 Solvent
Mutual regulatory interactions of the trunk gap genes during blastoderm patterning in the hemipteran Oncopeltus fasciatus
Mutually Opposite Effects of Dopamine center dot HCl and Chlorpromazine center dot HCl on the Thickness of Liposomal Lipid Bilayers
Mutual Coupling Compensation for Direction-of-Arrival Estimations Using the Receiving-Mutual-Impedance Method
Mutual Amplify-and-Forward Cooperation Using Modified STBC in OFDMA System
Mutual information via thermodynamics: three different approaches
Mutual Development: The Software Engineering Context of End-User Development
Mutually independent Hamiltonian cycles in dual-cubes
Mutuality's Prospective Beneficial Effects on Inflammation in Female Patients With Rheumatoid Arthritis
Mutualism between Consumers and Their Shared Resource Can Promote Competitive Coexistence
Mutual information in the Tangled Nature model
Mutual Solubility of Water and Structural/Positional Isomers of N-Alkylpyridinium-Based Ionic Liquids
Mutual Alignment of Block Copolymer-Magnetic Nanoparticle Composites in a Magnetic Field
Mutual trust and cooperation in the evolutionary hawks-doves game
Mutual Information Analysis of EEG Signals Indicates Age-Related Changes in Cortical Interdependence During Sleep in Middle-Aged Versus Elderly Women
Mutually-induced Conformational Switching of RNA and Coat Protein Underpins Efficient Assembly of a Viral Capsid
Mutual modulation between membrane-embedded receptor clustering and ligand binding in lipid membranes
Mutual Coupling Effects on Pattern Diversity Antennas for MIMO Femtocells
Mutually Positive Regulatory Feedback Loop between Interferons and Estrogen Receptor-alpha in Mice: Implications for Sex Bias in Autoimmunity
Mutual Interaction and Reciprocal Down-Regulation Between c-met and Insulin Receptor Substrate-1
Mutual Regulation of Src Family Kinases and the Neurotrophin Receptor TrkB
Mutual assessment via visual status signals in Polistes dominulus wasps
Mutual interaction of Faraday rotation and Cotton-Mouton phase shift in JET polarimetric measurements
Mutually exclusive expression of DLX2 and DLX5/6 is associated with the metastatic potential of the human breast cancer cell line MDA-MB-231
Mutually Disjoint Steiner Systems S(5,8,24) and 5-(24,12,48) Designs
Mutual Solubility of Pseudobinary Systems Containing Vegetable Oils and Anhydrous Ethanol from (298.15 to 333.15) K
Mutual Dependence of Mob1 and the Chromosomal Passenger Complex for Localization during Mitosis
Mutual Solubility for Systems Composed of Vegetable Oil plus Ethanol plus Water at Different Temperatures
Mutual reproductive dependence of distylic Cordia leucocephala (Cordiaceae) and oligolectic Ceblurgus longipalpis (Halictidae, Rophitinae) in the Caatinga
Mutual Relationship between Stacking and Hydrogen Bonding in DNA. Theoretical Study of Guanine-Cytosine, Guanine-5-methylcytosine, and Their Dimers
Mutual Effects of Caveolin and Nerve Growth Factor Signaling in Pig Oligodendrocytes
Mutual coupling compensation based on direct data domain algorithms
Mutual dependency of mechanical properties and contiguity in W-Cu composites
Mutual coupling reduction of microstrip antenna array using double negative substrate
Mutual Coupling Reduction in Patch Antenna Arrays Using a UC-EBG Superstrate
Mutual diffusion in a binary isotopic mixture
Mutual regulation of plant phospholipase D and the actin cytoskeleton
Mutual awareness: Enhanced by interface design and improving team performance in incident diagnosis under computerized working environment
Mutually Exclusive Uncertainty Relations
Mutual dilution of infection by an introduced parasite in native and invasive stream fishes across Hawaii
Mutual Authentication Protocol for Role-Based Access Control Using Mobile RFID
Mutual trust method for forwarding information in wireless sensor networks using random secret pre-distribution
Mutual effects of paraffin waxes and clathrate hydrates: A multiphase integrated thermodynamic model and experimental measurements
Mutual inductance and magnetic force calculations for coaxial bitter disk coils (Pancakes)
Mutual Coupling Reduction in MIMO Patch Antenna Array Using Complementary Split Ring Resonators Defected Ground Structure
Mutualistic association of rotifer Philodina roseola with the branchiuran fish ectoparasite Argulus bengalensis at its embryonic stage
Mutual amplification of HNF4 alpha and IL-1R1 composes an inflammatory circuit in Helicobacter pylori associated gastric carcinogenesis
Mutual Coupling Reduction in CBS Antenna Arrays by Utilizing Tuned EM-EBG and Non-planar Ground Plane
Mutualism exploitation: predatory drosophilid larvae sugar-trap ants and jeopardize facultative ant-plant mutualism
Mutualism Persistence and Abandonment during the Evolution of the Mycorrhizal Symbiosis
Mutually exclusive extracellular signal-regulated kinase pathway mutations are present in different stages of multi-focal pulmonary Langerhans cell histiocytosis supporting clonal nature of the disease
Mutual Coupling Mitigation in Broadband Multiple-Antenna Communication Systems Using Feedforward Technique
Mutualistic symbiosis with ophiuroids limited the impact of the Deepwater Horizon oil spill on deep-sea octocorals
Mutual solubility of water and hydrophobic ionic liquids in the presence of hydrochloric acid
Mutually Responsive Orientation: A novel observational assessment of mother-child mealtime interactions
Mutual interference reduces offspring production in abrood-guarding bethylid wasp
Mutual diffusion in polymer solutions: Spanning phase diagrams
Mutualism with aggressive wood-degrading Flavodon ambrosius (Polyporales) facilitates niche expansion and communal social structure in Ambrosiophilus ambrosia beetles
Mutual Information Bounds via Adjacency Events
Mutual synchronization of nano-oscillators driven by pure spin current
Mutually honest? Physiological "qualities' signalled by colour ornaments in monomorphic king penguins
Mutual regulation causes co-entrainment between a synthetic oscillator and the bacterial cell cycle
Mutual activation of blast furnace slag and a high-calcium fly ash rich in free lime and sulfates
Mutuality in health care: review, concept analysis and ways forward
Mutually exclusive RNA secondary structures regulate translation initiation of DinQ in Escherichia coli
Mutual synchronization behavior for chaotic systems via limited capacity communication channels
Mutual Coupling Reduction of a Closely Spaced Four-Element MIMO Antenna System Using Discrete Mushrooms
Mutually Beneficial Confluent Routing
Mutual seismic assessment and isolation of different art objects
Mutual diffusion diagram of liquid-liquid interfaces for morphological control of NaCl crystals
Mutual Separation of Indium, Gallium, and Zinc with the Amic Acid-type Extractant D2EHAG Containing Glycine and Amide Moieties
Mutual interference between Cytomegalovirus and Reconstitution of Protective immunity after Hematopoietic Cell Transplantation
Mutual Forbearance and Competition Among Security Analysts
Mutual information based weight initialization method for sigmoidal feedforward neural networks
Mutual capacitance of liquid conductors in deformable tactile sensing arrays
Mutually Unbiased Maximally Entangled Bases for the Bipartite System
Mutual Coupling Reduction by Novel Fractal Defected Ground Structure Bandgap Filter
Mutual Information-Based Multi-AUV Path Planning for Scalar Field Sampling Using Multidimensional RRT*
Mutual information network-based support vector machine for identification of rheumatoid arthritis-related genes
Mutual and intermittent enhancements of synchronization transitions by autaptic and synaptic delay in scale-free neuron networks
Mutual enhancing effects of the sigma-hole interactions and halogen/hydrogen-bonded interactions in the iodine-ylide containing complexes
Mutual Interference Suppression Using Clipping and Weighted-Envelope Normalization for Automotive FMCW Radar Systems
母兔繁殖障碍综合征的病因分析及防制
木托盘受力性能理论分析及有限元模拟
Mutual storage mode ion/ion reactions in a hybrid linear ion trap
Mutual blood donation is safer at small blood collection stations in China
Mutual promotion effect of Pr and Mg co-substitution on structure and multiferroic properties of BiFeO3 ceramic
Mutual Coupling Reduction of Dual-Frequency Patch Antenna Arrays
Mutually exclusive signaling signatures define the hepatic and pancreatic progenitor cell lineage divergence
Mutual inhibition and capacity sharing during parallel preparation of serial eye movements
Mutual Solubility of Hydrophobic Ionic Liquids and Water in Liquid-Liquid Two-phase Systems for Analytical Chemistry
Mutual Diffusion and Relaxation at Polymer/Polymer Interfaces
Mutual Coupling Effects for Radar Cross Section (RCS) of a Series-Fed Dipole Antenna Array
Mutual influence of two nonionic surfactants mixture and propanol on their volumetric properties in aqueous solution
Mutually exclusive distribution of the sap and eag S-layer genes and the lytB/lytA cell wall hydrolase genes in Bacillus thuringiensis
Mutual Repression by Bantam miRNA and Capicua Links the EGFR/MAPK and Hippo Pathways in Growth Control
Mutually-modulated cross-gain modulation and slow light
Mutual action of anticancer and antiparasitic drugs: are there any shared targets?
Mutual Exclusivity of Hyaluronan and Hyaluronidase in Invasive Group A Streptococcus
Mutual cooperative effects between single- and two-photon super-fluorescent processes through vacuum field
Mutual antagonism between IP3RII and miRNA-133a regulates calcium signals and cardiac hypertrophy
Mutual information-based feature selection and partition design in fuzzy rule-based classifiers from vague data
Mutual interplay between pnicogen bond and dihydrogen bond in HMH center dot center dot center dot HCN center dot center dot center dot PH2X complexes (M = Be, Mg, Zn; X = H, F, Cl)
Mutual Coupling Reduction in Waveguide-Slot-Array Antennas Using Electromagnetic Bandgap (EBG) Structures
Mutual Information Optimization for Mass Spectra Data Alignment
Mutually helping microbes can evolve by hitchhiking
Mutualists and antagonists drive among-population variation in selection and evolution of floral display in a perennial herb
Mutualistic Polydnaviruses Share Essential Replication Gene Functions with Pathogenic Ancestors
Mutual Ferromagnetic-Ferroelectric Coupling in Multiferroic Copper-Doped ZnO
Mutual synchronization of two stacks of intrinsic Josephson junctions in cuprate superconductors
Mutual Coupling Effect on Ultrawideband Linear Antenna Array Performance
Mutual influence of serotonin and dopamine on the functioning of the dorsal striatum and motor activity (hypothetical mechanism)
Mutual information-based selection of optimal spatial-temporal patterns for single-trial EEG-based BCIs
Mutual Solubilities of water and hydrophobic ionic liquids
Mutual solubilities of water and the [C(n)mim][Tf(2)N] hydrophobic ionic liquids
Mutual changes in bitumen and rubber related to the production of asphalt rubber binders
Mutual interactions between flavonoids and enzymatic and transporter elements responsible for flavonoid disposition via phase II metabolic pathways
Mutual exclusion of ASXL1 and NPM1 mutations in a series of acute myeloid leukemias
Mutual influences between the main olfactory and vomeronasal systems in development and evolution
Mutualistic interactions on a knife-edge between saprotrophy and pathogenesis
Mutual impacts of product standardization and supply chain design
Mutual Chern-Simons effective theory of doped antiferromagnets
Mutual diffusion coefficients of heptane isomers in nitrogen: A molecular dynamics study
Mutual enhancement of cathodoluminescence and organic electroluminescence in SiO2/C-9-PPV heterogeneous junction
Mutual Fund Trading Pressure: Firm-Level Stock Price Impact and Timing of SEOs
Mutual optical injection in coupled DBR laser pairs
Mutual Impedance of Small Ring-Type Coils for Multiwinding Induction Heating Appliances
Mutualism meltdown in insects: bacteria constrain thermal adaptation
Mutually Exclusive Expression of G alpha ia and G alpha 14 Reveals Diversification of Taste Receptor Cells in Zebrafish
Mutual Inhibition between Kaposi's Sarcoma-Associated Herpesvirus and Epstein-Barr Virus Lytic Replication Initiators in Dually-Infected Primary Effusion Lymphoma
Mutual Diffusion and Microstructure Evolution at the Electrolyte-Anode Interface in Intermediate Temperature Solid Oxide Fuel Cell
Mutually catalyzed birth of population and assets in exchange-driven growth
Mutual injection phase locking coherent combination of solid-state lasers based on corner cube
Mutual exclusion of transcription factors and cell behaviour in the definition of vertebrate embryonic territories
Mutualism versus pathogenesis: the give-and-take in plant-bacteria interactions
Mutual funds performance appraisal using stochastic multicriteria acceptability analysis
Mutual Fund Tax Clienteles
Mutual coherence and spin squeezing in double-well atomic condensates
Mutualistic fungal endophytes in the Triticeae - survey and description
Mutual recognition of TNT using antibodies polymeric shell having CdS
Mutual, reciprocal SDF-1/CXCR4 interactions between hematopoietic and bone marrow stromal cells regulate human stem cell migration and development in NOD/SCID chimeric mice
Mutual Coupling in Phased Arrays: A Review
Mutual information spectrum for selection of event-related spatial components. Application to eloquent motor cortex mapping
Mutual effects of disorder and order in fusion proteins between intrinsically disordered domains and fluorescent proteins
Mutual solubility measurements and correlations of imidazolium-based ionic liquid mixtures with alcohols
Mutual separation of americium(III) and europium(III) using glycolamic acid and thioglycolamic acid
Mutual control of intracellular localisation of the patterning proteins AtMYC1, GL1 and TRY/CPC in Arabidopsis
Mutual role of PGRN/TNF-alpha on osteopenia developing in obesity%26apos;s inflammation state
Mutual influence between conventional and unconventional lithium bonds
Mutually Injection-Locked Tunable Laser Based on GS-RSOAs for L-Band Generation
Mutual relationships between transcription and pre-mRNA processing in the synthesis of mRNA
Mutual exclusivity analysis identifies oncogenic network modules
Mutual regulation between the spindle checkpoint and APC/C
Mutual influence between anion-pi and pnicogen bond interactions: The enhancement of P center dot center dot center dot N and P center dot center dot center dot O interactions by an anion-pi bond
Mutuality in Discrete and Compositional Information: Perspectives for Synthetic Genetic Codes
Mutuality as a control for information asymmetry: A historical analysis of the claims experience of mutual and stock fire insurance companies in Sweden, 1889 to 1939
Mutual induction of magnetic 3d and 4f order in multiferroic hexagonal ErMnO3
Mutual Repression Enhances the Steepness and Precision of Gene Expression Boundaries
Mutual action of copper (II) and a nonionic surfactant (oxyethylated alcohols) on their simultaneous removal by a neutral hyper-cross-linked polystyrene adsorbent
Mutual coupling suppression in closely spaced antennas
Mutual Information, Relative Entropy, and Estimation in the Poisson Channel
Mutual validation of GNSS height measurements and high-precision geometric-astronomical leveling
Mutual Best Friendship Involvement, Best Friends' Rejection Sensitivity, and Psychological Maladaptation
Mutual information in classical spin models
Mutual boosting of the saturation scales in colliding nuclei
Mutual Benefits: Developing Relational Service Approaches Within Centrelink
Mutuality in leader-subordinate empowerment expectation: Its impact on role ambiguity and intrinsic motivation
Mutual Coupling Reduction Between Planar Antennas by Using a Simple Microstrip U-Section
Mutualistic Interactions Drive Ecological Niche Convergence in a Diverse Butterfly Community
Mutual influence of crosshatch angle and superficial roughness of honed surfaces on friction in ring-pack tribo-system
Mutual Information-Based Supervised Attribute Clustering for Microarray Sample Classification
Mutual Fund Tournaments: The Sorting Bias and New Evidence
Mutual solubility of CH4, CO2, H2S, and their mixtures in brine under subsurface disposal conditions
Mutual information after a local quench in conformal field theory
Mutual Interference of Two Debris Flow Deposits Delivered in a Downstream River Reach
Mutual Dependence of Foxo3a and PGC-1 alpha in the Induction of Oxidative Stress Genes
Mutual influences between partners%26apos; hormones shape conflict dialog and relationship duration at the initiation of romantic love
Mutually unbiased bases and generalized Bell states
Mutual mate choice in the potbellied seahorse (Hippocampus abdominalis)
Mutual Interference between Intramolecular Proton Transfer Sites through the Adjoining pi-Conjugated System in Schiff Bases of Double-Headed, Fused Salicylaldehydes
Mutual information-based feature selection for intrusion detection systems
Mutually exclusive STAT1 modifications identified by Ubc9/substrate dimerization-dependent SUMOylation
Mutual repression between Pax3 and Pax6 is involved in the positioning of ophthalmic trigeminal placode in avian embryo
Mutualism Breakdown by Amplification of Wolbachia Genes
Mutual reinforcement of inflammation and carcinogenesis by the Helicobacter pylori CagA oncoprotein
Mutual mother-offspring vocal recognition in an ungulate hider species (Capra hircus)
Mutualism and evolutionary multiplayer games: revisiting the Red King
Mutual regulation between deubiquitinase CYLD and retroviral oncoprotein Tax
Mutual-information-based image to patient re-registration using intraoperative ultrasound in image-guided neurosurgery
Mutual fund volatility timing and management fees
Mutually reinforcing patterning mechanisms
Mutually reinforcing patterning mechanisms: authors' reply
Mutual selection equilibrium theory for rainbow-shaped mutually pumped phase conjugation
Mutually exclusive expression of human red and green visual pigment-reporter transgenes occurs at high frequency in murine cone photoreceptors
Mutual regulation of hypoxic and retinoic acid related signalling in tubular proximal cells
Mutual coupling reduction in patch antenna arrays by using a planar EBG structure and a multilayer dielectric substrate
Mutual Coupling Reduction Using EBG in Steering Antennas
Mutual separation and determination of Th(IV) and U(VI) using arsenazo III as a dye collector reagent by flotation-spectrophotometric method
Mutual regulation between metabotropic glutamate type 1 alpha receptor and caveolin proteins: from traffick to constitutive activity
Mutual Information-Based Inputs Selection for Electric Load Time Series Forecasting
Mutual adjustment search with incentive for supply chain planning coordination
Mutual wear evaluation of resin composites when opposing enamel and dentin
Mutual external inductance in stripline structures
Mutual Diffusion Occurring at the Interface between La0.6Sr0.4Co0.8Fe0.2O3 Cathode and Gd-doped Ceria Electrolyte during IT-SOFC Cell Preparation
Mutual halo effects in cultural production: the case of modernist architecture