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Amyloid-beta(25-35) Upregulates Endogenous Neuroprotectant Neuroglobin via NF kappa B Activation in vitro
Amyloid Assembly Endows Gad m 1 with Biomineralization Properties
Amyloid assembly and disassembly
Amylibacter lutimaris sp nov., isolated from sea-tidal flat sediment
Amylase and protease activity in shrimps and prawn of Sundarbans, West Bengal, India
Amyloidosis: An Unusual Cause of Intestinal Pseudo-Obstruction
Amyloid blood biomarker detects Alzheimer's disease
Amyloid-like aggregation of designer bolaamphiphilic peptides: Effect of hydrophobic section and hydrophilic heads
Amyloid-beta (1-40) and Mortality in Patients With Non-ST-Segment Elevation Acute Coronary Syndrome A Cohort Study
Amyloodiniosis in cultured Dicentrarchus labrax: parasitological and molecular diagnosis, and an improved treatment protocol
Amyloid-beta Degradation and Neuroprotection of Dauricine Mediated by Unfolded Protein Response in a Caenorhabditis elegans Model of Alzheimer's disease
Amyloid Beta Deposition Could Cause Corneal Epithelial Cell Degeneration Associated with Increasing Apoptosis in APPswePS1 Transgenic Mice
Amyloid-beta(1)(-)(42) dynamically regulates the migration of neural stem/progenitor cells via MAPK-ERK pathway
Amyloid�β and tau are involved in sleep disorder in Alzheimer's disease by orexin�A and adenosine A(1) receptor
Amyloid Growth, Inhibition, and Real-Time Enzymatic Degradation Revealed with Single Conical Nanopore
Amyloid-β/Drug Interactions from Computer Simulations and Cell-Based Assays
Amyloid precursor protein is overexpressed in bladder cancer and contributes to the malignant bladder cancer cell behaviors.
Amyloid toxicity in Alzheimer’s disease
Amyloid burden is associated with cognition in a cross-sectional and short-term longitudinal manner in patients with mild cognitive impairment
Amynthas agrestis invasion increases microbial biomass in Mid-Atlantic deciduous forests
Amyopathic dermatomyositis or dermatomyositis-like skin disease: retrospective review of 16 cases with amyopathic dermatomyositis
Amyotrophic Lateral Sclerosis: An Emerging Era of Collaborative Gene Discovery
Amyotrophic lateral sclerosis progression and stability of brain-computer interface communication
Amyotrophic lateral sclerosis/motor neuron disease deaths in the United States, 1999-2009
Amyotrophic Lateral Sclerosis: Problems and Prospects
Amyotrophic Lateral Sclerosis and Pseudo-infarct Pattern on the Electrocardiogram
Amyotrophic lateral sclerosis and cancer: A register-based study in Sweden
Amyotrophic lateral sclerosis: Analysis of ALS cases in a predominantly admixed population of Ecuador
Amyotrophic Lateral Sclerosis and Spinocerebellar Ataxia Type 2 in a Family With Full CAG Repeat Expansions of ATXN2
Amyoplasia Involving Only the Upper Limbs or Only Involving the Lower Limbs with Review of the Relevant Differential Diagnoses
Amyotrophic lateral sclerosis-a model of corticofugal axonal spread
Amyotrophic lateral sclerosis and Huntington's disease: Neurodegenerative link or coincidence?
Amyotrophic lateral sclerosis-linked FUS/TLS alters stress granule assembly and dynamics
Amyotrophic Lateral Sclerosis in a Patient with a Family History of Huntington Disease: Genetic Counseling Challenges
Amyotrophic lateral sclerosis in pregnancy: clinical outcome during the post-partum period after stem cell transplantation into the frontal motor cortex
Amyotrophic lateral sclerosis: a long preclinical period?
Amyotrophic lateral sclerosis: cell vulnerability or system vulnerability?
Amyotrophic lateral sclerosis in literature, cinema and television
Amyotrophic lateral sclerosis: new ideas from cancer Comment
Amyotrophic lateral sclerosis: an update on recent genetic insights
Amyotrophic lateral sclerosis and parkinsonism in Papua, Indonesia: 2001-2012 survey results
Amyopathic Dermatomyositis Complicated with Eosinophilic Pneumonia
Amyoplasia Revisited
Amyotrophic lateral sclerosis in Sardinia (Italy): epidemiologic features from 1957 to 2000
Amyotrophic Lateral Sclerosis Descriptive Studies: Not Only Rates and Frequencies
Amyopathic dermatomyositis with lung involvement responsive to mycophenolate mofetil
Amyotrophic lateral sclerosis in Catalonia: A population based study
Amyotrophic lateral sclerosis in Sardinia, insular Italy, 1995-2009
Amyotrophic lateral sclerosis: is the astrocyte the cell primarily involved?
Amyotrophic Lateral Sclerosis survival analysis: Swallowing and non-oral feeding
Amyotrophic lateral sclerosis: a new missense mutation in the SOD1 gene
Amyotrophic Lateral Sclerosis: A Focus on Disease Progression
Amyopathic dermatomyositis: evidence of systemic associations
Amyotrophic lateral sclerosis and frontotemporal dementia: distinct and overlapping changes in eating behaviour and metabolism
Amyotrophic lateral sclerosis. Multisystem degeneration
Amyotrophic lateral sclerosis among cross-country skiers in Sweden
Amyotrophic Lateral Sclerosis and the Military A Population-based Study in the Danish Registries
Amyotrophic lateral sclerosis mortality rates in Chile: A population based study (1994-2010)
Amyopathic Dermatomyositis-Related Thrombophilia
Amyotrophic Lateral Sclerosis Genetic Studies: From Genome-wide Association Mapping to Genome Sequencing
Amyotrophic lateral sclerosis presentation of a human T-lymphotropic virus type-1 myelopathy - insight into pathogenesis
Amyotrophic lateral sclerosis and denervation alter sphingolipids and up-regulate glucosylceramide synthase
Amyotrophic Lateral Sclerosis: Review
Amyotrophic Lateral Sclerosis: the Role of Exercise
Amyotrophic lateral sclerosis progression: Iran-ALS clinical registry, a multicentre study
Amyotrophic lateral sclerosis patients show executive impairments on standard neuropsychological measures and an ecologically valid motor-free test of executive functions
Amyotrophic Lateral Sclerosis-associated Proteins TDP-43 and FUS/TLS Function in a Common Biochemical Complex to Co-regulate HDAC6 mRNA
Amyotrophic lateral sclerosis is a non-amyloid disease in which extensive misfolding of SOD1 is unique to the familial form
Amyotrophic lateral sclerosis in a patient with Kartagener syndrome
Amyotrophic Lateral Sclerosis Pathogenesis: A Journey Through the Secretory Pathway
Amyotrophic lateral sclerosis: dash-like accumulation of phosphorylated TDP-43 in somatodendritic and axonal compartments of somatomotor neurons of the lower brainstem and spinal cord
Amyotrophic lateral sclerosis and ocular flutter
Amyotrophic lateral sclerosis: gender differences in the use of mechanical ventilation
Amyotrophic Lateral Sclerosis
Amyotrophic lateral sclerosis and frontotemporal lobar degeneration: A spectrum of TDP-43 proteinopathies
Amyotrophic lateral sclerosis: current practice and future treatments
Amyotrophic lateral sclerosis, physical exercise, trauma and sports: Results of a population-based pilot case-control study
Amyotrophic Lateral Sclerosis-Frontotemporal Lobar Dementia in 3 Families With p.Ala382Thr TARDBP Mutations
Amyotrophic lateral sclerosis Prospective study on respiratory parameters
Amyotrophic lateral sclerosis and sarcoidosis: A difficult differential diagnosis
Amyotrophic lateral sclerosis: moving towards a new classification system
Amyotrophic lateral sclerosis: A higher than expected incidence in people over 80 years of age
Amyotrophic lateral sclerosis in Brazil: Case series and review of the Brazilian literature