Dissection of genetic factors associated with amyotrophic lateral sclerosis.
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The Unfolded Protein Response and the Role of Protein Disulfide Isomerase in NeurodegenerationClinical and genetic basis of familial amyotrophic lateral sclerosisApplications of Induced Pluripotent Stem Cells in Studying the Neurodegenerative DiseasesEmerging mechanisms of molecular pathology in ALSA novel SOD1-ALS mutation separates central and peripheral effects of mutant SOD1 toxicityGene expression profiling for human iPS-derived motor neurons from sporadic ALS patients reveals a strong association between mitochondrial functions and neurodegeneration.Aldehyde Dehydrogenases 1A2 Expression and Distribution are Potentially Associated with Neuron Death in Spinal Cord of Tg(SOD1*G93A)1Gur Mice.Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS.U1 snRNP is mislocalized in ALS patient fibroblasts bearing NLS mutations in FUS and is required for motor neuron outgrowth in zebrafishA fruitful endeavor: modeling ALS in the fruit flyEvidence for fungal infection in cerebrospinal fluid and brain tissue from patients with amyotrophic lateral sclerosis.Glial Regulation of the Neuronal Connectome through Local and Long-Distant Communication.Brca1 is expressed in human microglia and is dysregulated in human and animal model of ALS.Special Issue on amyotrophic lateral sclerosis.Rodent Models of Amyotrophic Lateral SclerosisSingle-nucleotide Polymorphism rs2275294 in ZNF512B is not Associated with Susceptibility to Amyotrophic Lateral Sclerosis in a Large Chinese CohortUse of biomarkers in ALS drug development and clinical trialsChromosomal microarray analysis in clinical evaluation of neurodevelopmental disorders-reporting a novel deletion of SETDB1 and illustration of counseling challengeDisease origin and progression in amyotrophic lateral sclerosis: an immunology perspective.MicroRNAs as potential circulating biomarkers for amyotrophic lateral sclerosis.The expanding syndrome of amyotrophic lateral sclerosis: a clinical and molecular odysseyMicroglia Responses in Acute and Chronic Neurological Diseases: What Microglia-Specific Transcriptomic Studies Taught (and did Not Teach) Us.Targeting mitochondrial metal dyshomeostasis for the treatment of neurodegeneration.Genetics of FTLD: overview and what else we can expect from genetic studies.ALS: Recent Developments from Genetics Studies.Pathogenesis of amyotrophic lateral sclerosis.Liver X receptors: from cholesterol regulation to neuroprotection-a new barrier against neurodegeneration in amyotrophic lateral sclerosis?TDP-43/FUS in motor neuron disease: Complexity and challenges.Protein Disulphide Isomerases: emerging roles of PDI and ERp57 in the nervous system and as therapeutic targets for ALS.Expression and Distribution of Arylsulfatase B are Closely Associated with Neuron Death in SOD1 G93A Transgenic Mice.De novo FUS P525L mutation in Juvenile amyotrophic lateral sclerosis with dysphonia and diplopia.Fine-Tuning ER Stress Signal Transducers to Treat Amyotrophic Lateral Sclerosis.Novel FUS mutations identified through molecular screening in a large cohort of familial and sporadic amyotrophic lateral sclerosis.ALS-linked protein disulfide isomerase variants cause motor dysfunction.Accrued somatic mutations (nucleic acid changes) trigger ALS: 2005-2015 update.Identification of rare protein disulfide isomerase gene variants in amyotrophic lateral sclerosis patients.Vitamin D is Not a Protective Factor in ALS.Molecular Chaperones in the Pathogenesis of Amyotrophic Lateral Sclerosis: The Role of HSPB1.Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?Amyotrophic lateral sclerosis - frontotemporal spectrum disorder (ALS-FTSD): Revised diagnostic criteria.
P2860
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P2860
Dissection of genetic factors associated with amyotrophic lateral sclerosis.
description
article científic
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article scientifique
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articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
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artigo científico
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artikel ilmiah
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artikull shkencor
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artículo científico
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name
Dissection of genetic factors associated with amyotrophic lateral sclerosis.
@en
type
label
Dissection of genetic factors associated with amyotrophic lateral sclerosis.
@en
prefLabel
Dissection of genetic factors associated with amyotrophic lateral sclerosis.
@en
P1476
Dissection of genetic factors associated with amyotrophic lateral sclerosis.
@en
P2093
Claire S Leblond
Hannah M Kaneb
P304
P356
10.1016/J.EXPNEUROL.2014.04.013
P407
P478
P577
2014-04-26T00:00:00Z