Amyotrophic lateral sclerosis: an update on recent genetic insights.
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Recent advances in amyotrophic lateral sclerosisGenotype-phenotype correlations of amyotrophic lateral sclerosisThe Function of Autophagy in Neurodegenerative DiseasesClinical and genetic basis of familial amyotrophic lateral sclerosisC9orf72's Interaction with Rab GTPases-Modulation of Membrane Traffic and AutophagyCalcium dysregulation links ALS defective proteins and motor neuron selective vulnerabilityLegal but lethal: functional protein aggregation at the verge of toxicityRare Manifestation of a c.290 C>T, p.Gly97Glu VCP MutationAssisting persons with advanced amyotrophic lateral sclerosis in their leisure engagement and communication needs with a basic technology-aided program.Sigma-1 receptor chaperones in neurodegenerative and psychiatric disordersThe Sigma-1 Receptor as a Pluripotent Modulator in Living Systems.Evidence for fungal infection in cerebrospinal fluid and brain tissue from patients with amyotrophic lateral sclerosis.Rare variants at 16p11.2 are associated with common variable immunodeficiencyRegenerative cellular therapies for neurologic diseasesStructural analysis of disease-related TDP-43 D169G mutation: linking enhanced stability and caspase cleavage efficiency to protein accumulation.The Association between C9orf72 Repeats and Risk of Alzheimer's Disease and Amyotrophic Lateral Sclerosis: A Meta-Analysis.A critical role of Hrd1 in the regulation of optineurin degradation and aggresome formation.Could Sirtuin Activities Modify ALS Onset and Progression?Copy Number Variations in Amyotrophic Lateral Sclerosis: Piecing the Mosaic Tiles Together through a Systems Biology Approach.Label-Free LC-MS/MS Proteomic Analysis of Cerebrospinal Fluid Identifies Protein/Pathway Alterations and Candidate Biomarkers for Amyotrophic Lateral SclerosisThe heat shock response in neurons and astroglia and its role in neurodegenerative diseases.Cognitive dysfunction in hereditary spastic paraplegias and other motor neuron disorders.Matrin3 binds directly to intronic pyrimidine-rich sequences and controls alternative splicing.A basic technology-aided programme for leisure and communication of persons with advanced amyotrophic lateral sclerosis: performance and social rating.A chemical chaperone-based drug candidate is effective in a mouse model of amyotrophic lateral sclerosis (ALS).G protein-coupled receptor 26 immunoreactivity in intranuclear inclusions associated with polyglutamine and intranuclear inclusion body diseases.Exome sequencing uncovers hidden pathways in familial and sporadic ALS.Preclinical progression of neurodegenerative diseases
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P2860
Amyotrophic lateral sclerosis: an update on recent genetic insights.
description
2013 թվականի հոկտեմբերի 2-ին հրատարակված գիտական հոդված
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article científic
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article scientifique
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articol științific
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articolo scientifico
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artigo científico
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artigo científico
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artigo científico
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artikel ilmiah
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artikull shkencor
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name
Amyotrophic lateral sclerosis: an update on recent genetic insights.
@en
type
label
Amyotrophic lateral sclerosis: an update on recent genetic insights.
@en
prefLabel
Amyotrophic lateral sclerosis: an update on recent genetic insights.
@en
P2093
P2860
P1433
P1476
Amyotrophic lateral sclerosis: an update on recent genetic insights.
@en
P2093
Kensuke Ikenaka
Masahisa Katsuno
Shinsuke Ishigaki
Yohei Iguchi
P2860
P2888
P304
P356
10.1007/S00415-013-7112-Y
P50
P577
2013-10-02T00:00:00Z
P6179
1008654030