Home
|
Learning Center
|
中文版
Publications
站内成果搜索:
搜索
ATP13A2 G2236A variant is rare in patients with early-onset Parkinson's disease and familial Parkinson's disease from mainland China
ATP13A2 Variants in Early-Onset Parkinson's Disease Patients and Controls
ATP11B mediates platinum resistance in ovarian cancer
ATP13A2 mutations impair mitochondrial function in fibroblasts from patients with Kufor-Rakeb syndrome
ATP13A2与帕金森病相关性的研究进展
ATP13A2 deficiency induces a decrease in cathepsin D activity, fingerprint-like inclusion body formation, and selective degeneration of dopaminergic neurons
ATP11C Facilitates Phospholipid Translocation across the Plasma Membrane of All Leukocytes
ATP1A3 Mutation in Adult Rapid-Onset Ataxia
ATP1A1-Mediated Src Signaling Inhibits Coronavirus Entry into Host Cells
ATP13A2 Mutations (PARK9) Cause Neurodegeneration with Brain Iron Accumulation
ATP11A is a novel predictive marker for metachronous metastasis of colorectal cancer
ATP11C Targets Basolateral Bile Salt Transporter Proteins in Mouse Central Hepatocytes
ATP1B3: a virus-induced host factor against EV71 replication by up-regulating the production of type-I interferons
ATP13A3 and caveolin-1 as potential biomarkers for difluoromethylornithine-based therapies in pancreatic cancers
ATP11C is a major flippase in human erythrocytes and its defect causes congenital hemolytic anemia
ATP1A2 Mutations in Migraine: Seeing through the Facets of an Ion Pump onto the Neurobiology of Disease
ATP13A2 Variability in Taiwanese Parkinson's Disease
ATP13A2 regulates mitochondrial bioenergetics through macroautophagy
ATP13A2/PARK9 Regulates Secretion of Exosomes and alpha-Synuclein
ATP13A2 (PARK9) polymorphisms influence the neurotoxic effects of manganese
ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia
ATP13A2/PARK9 regulates endo-/lysosomal cargo sorting and proteostasis through a novel PI(3,5)P2-mediated scaffolding function
ATP1A3 mutant patient with alternating hemiplegia of childhood and brain spectroscopic abnormalities
ATP11C mutation is responsible for the defect in phosphatidylserine uptake in UPS-1 cells
ATP1A3 mutations can cause progressive auditory neuropathy: a new gene of auditory synaptopathy
ATP13A2 (PARK9) protein levels are reduced in brain tissue of cases with Lewy bodies
ATP1A3 mutations What is the phenotype?
ATP1A3 spectrum disorders: A video-documented history of 7 genetically confirmed early onset cases
ATP1A3基因突变致儿童期起病快发病性肌张力障碍-帕金森综合征一家系并文献复习
ATP13A2基因Arg294Gln多态性与新疆地区维吾尔族及汉族帕金森病的相关性
ATP2A2通过钙离子浓度变化参与肿瘤发生机制的研究进展
ATP2B1基因多态性与老年高血压动脉硬化的相关性
ATP2B1 and blood pressure: from associations to pathophysiology
ATP2A3 gene as an important player for resveratrol anticancer activity in breast cancer cells
ATP2C2 and DYX1C1 are putative modulators of dyslexia-related MMR
ATP2B1 Gene Silencing Increases NO Production Under Basal Conditions Through the Ca2+/calmodulin/eNOS Signaling Pathway in Endothelial Cells
ATP2B1 gene Silencing Increases Insulin Sensitivity through Facilitating Akt Activation via the Ca2+/calmodulin Signaling Pathway and Ca2+-associated eNOS Activation in Endothelial Cells
ATP3 and MTP3: Easily Prepared Stable Perruthenate Salts for Oxidation Applications in Synthesis
ATP4B在不同程度胃黏膜病变中的表达及其与幽门螺杆菌感染的关系
ATP4A autoimmunity and Helicobacter pylori infection in children with type 1 diabetes
ATP4a is required for development and function of the Xenopus mucociliary epidermis - a potential model to study proton pump inhibitor-associated pneumonia
ATP4, THE STRUCTURAL GENE FOR YEAST F0F1 ATPASE SUBUNIT-4
ATP4a Is Required for Wnt-Dependent Foxj1 Expression and Leftward Flow in Xenopus Left-Right Development
ATP4A autoimmunity in pediatric patients with type 1 diabetes and its relationship to blood count, iron metabolism, and vitamin B12
ATP5H/KCTD2 locus is associated with Alzheimer%26apos;s disease risk
ATP5B regulates mitochondrial fission and fusion in mammalian cells
ATP5b and beta 2-microglobulin are predictive markers for the prognosis of patients with gallbladder cancer
ATP5J and ATP5H Proactive Expression Correlates with Cardiomyocyte Mitochondrial Dysfunction Induced by Fluoride
ATP5B and ETFB metabolic markers in children with congenital hydronephrosis
ATP5A1 and ATP5B are highly expressed in glioblastoma tumor cells and endothelial cells of microvascular proliferation
ATP5J促进猪繁殖与呼吸综合征病毒复制研究
ATP6V1B1 mutations in distal renal tubular acidosis and sensorineural hearing loss: clinical and genetic spectrum of five families
ATP6V0C Knockdown in Neuroblastoma Cells Alters Autophagy-Lysosome Pathway Function and Metabolism of Proteins that Accumulate in Neurodegenerative Disease
ATP6v0d2 deficiency increases bone mass, but does not influence ovariectomy-induced bone loss
ATP6AP1 deficiency causes an immunodeficiency with hepatopathy, cognitive impairment and abnormal protein glycosylation
ATP6V0A1 Polymorphism and MicroRNA-637 A Pathogenetic Role for MicroRNAs in Essential Hypertension at Last?
ATP6AP2/(Pro)renin Receptor Contributes to Glucose Metabolism via Stabilizing the Pyruvate Dehydrogenase E1 beta Subunit
ATP6V0A2基因突变致皮肤松弛症一例及文献复习
ATP6AP2 over-expression causes morphological alterations in the hippocampus and in hippocampus-related behaviour
ATP6V0A2 -related cutis laxa in 10 novel patients: Focus on clinical variability and expansion of the phenotype
ATP7B antisense oligodeoxynucleotides increase the cisplatin sensitivity of human ovarian cancer cell line SKOV3ipl
ATP7B Variants as Modulators of Copper Dyshomeostasis in Alzheimer%26apos;s Disease
ATP7B基因重组腺病毒载体对肝豆状核变性患者肝细胞的影响
ATP7B siRNA阳离子纳米脂质体逆转卵巢癌细胞株顺铂耐药的体内外实验研究
ATP7A Transgenic and nontransgenic mice are resistant to high copper exposure
ATP7B expression in human breast epithelial cells is mediated by lactational hormones
ATP7B Gene Mutations in Croatian Patients with Wilson Disease
ATP7B detoxifies silver in ciliated airway epithelial cells
ATP7B expression is associated with in vitro sensitivity to cisplatin in non-small cell lung cancer
ATP7B expression confers multidrug resistance through drug sequestration
ATP7B和PCNA在大鼠、小鼠空肠及肾的表达
ATP7A-related copper transport diseases-emerging concepts and future trends
ATP7A Gene Addition to the Choroid Plexus Results in Long-term Rescue of the Lethal Copper Transport Defect in a Menkes Disease Mouse Model
ATP7B Mutation Detection and Pathogenicity Analysis: One Atypical Case of Wilson's Disease with Adrenocortical Insufficiency
ATP7B rs9535826 is associated with gastrointestinal toxicity of platinum-based chemotherapy in nonsmall cell lung cancer patients
ATP8基因在小鼠单个GV期卵母细胞中的表达和生物信息学分析
ATP8B1 and ABCB11 Analysis in 62 Children with Normal Gamma-Glutamyl Transferase Progressive Familial Intrahepatic Cholestasis (PFIC): Phenotypic Differences Between PFIC1 and PFIC2 and Natural History
ATP8B1 Gene Expression Is Driven by a Housekeeping-Like Promoter Independent of Bile Acids and Farnesoid X Receptor
ATP8B1 is essential for maintaining normal hearing
ATP8B1-mediated spatial organization of Cdc42 signaling maintains singularity during enterocyte polarization
ATP9B, a P4-ATPase (a Putative Aminophospholipid Translocase), Localizes to the trans-Golgi Network in a CDC50 Protein-independent Manner
ATP: a mediator for HCl-induced TRPV1 activation in esophageal mucosa
ATP:RNA腺苷酰转移酶的纯化及其应用