Genetic overlap between apparently sporadic motor neuron diseases. - Test2 - elhamkhani - TriplyDB

Genetic overlap between apparently sporadic motor neuron diseases.

Genetic overlap between apparently sporadic motor neuron diseases.

http://www.wikidata.org/entity/Q34479235

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Genotype-phenotype correlations of amyotrophic lateral sclerosis Neuropathology of Amyotrophic Lateral Sclerosis and Its Variants.A genetic screen identifies Tor as an interactor of VAPB in a Drosophila model of amyotrophic lateral sclerosis.Regulation of postsynaptic function by the dementia-related ESCRT-III subunit CHMP2B Rab8, POSH, and TAK1 regulate synaptic growth in a Drosophila model of frontotemporal dementia Controversies and priorities in amyotrophic lateral sclerosis.Variants within the SP110 nuclear body protein modify risk of canine degenerative myelopathy.Clinical neurogenetics: amyotrophic lateral sclerosis.Clinical and genetic heterogeneity of amyotrophic lateral sclerosis.Genetic counselling in ALS: facts, uncertainties and clinical suggestions.Physiological and pathological roles of exosomes in the nervous system.Coordination of synaptic vesicle trafficking and turnover by the Rab35 signaling network.A transgenic mouse expressing CHMP2Bintron5 mutant in neurons develops histological and behavioural features of amyotrophic lateral sclerosis and frontotemporal dementia.Prediction of functional loss of human angiogenin mutants associated with ALS by molecular dynamics simulations.The Genetics of Monogenic Frontotemporal Dementia.Synaptic dysfunction and altered excitability in C9ORF72 ALS/FTD.Comparison of the clinical and cognitive features of genetically positive ALS patients from the largest tertiary center in Serbia.Optineurin: A Coordinator of Membrane-Associated Cargo Trafficking and Autophagy.Role of Optineurin in the Mitochondrial Dysfunction: Potential Implications in Neurodegenerative Diseases and Cancer.C9orf72, a protein associated with amyotrophic lateral sclerosis (ALS) is a guanine nucleotide exchange factor The El Escorial criteria: Strengths and weaknesses Time to generalization and prediction of survival in patients with amyotrophic lateral sclerosis: a retrospective observational study Clinical variability and additional mutations in amyotrophic lateral sclerosis patients with p.N352S mutations inTARDBP

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Genetic overlap between apparently sporadic motor neuron diseases.

http://www.wikidata.org/entity/Q34479235

description

2012 nî lūn-bûn

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2012 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2012年の論文

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2012年論文

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2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

name

Genetic overlap between apparently sporadic motor neuron diseases.

@ast

Genetic overlap between apparently sporadic motor neuron diseases.

@en

Genetic overlap between apparently sporadic motor neuron diseases.

@nl

type

label

Genetic overlap between apparently sporadic motor neuron diseases.

@ast

Genetic overlap between apparently sporadic motor neuron diseases.

@en

Genetic overlap between apparently sporadic motor neuron diseases.

@nl

prefLabel

Genetic overlap between apparently sporadic motor neuron diseases.

@ast

Genetic overlap between apparently sporadic motor neuron diseases.

@en

Genetic overlap between apparently sporadic motor neuron diseases.

@nl

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JOURNAL.PONE.0048983

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Genetic overlap between apparently sporadic motor neuron diseases.

@en

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Anneke J van der Kooi

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Dennis Dooijes

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Eric A M Hennekam

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Helenius J Schelhaas

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Lotte Vlam

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Marianne de Visser

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Michael A van Es

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W-Ludo van der Pol

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P2860

SOD1 and amyotrophic lateral sclerosis: mutations and oligomerization

The heritability of amyotrophic lateral sclerosis in a clinically ascertained United States research registry

ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)

CHMP7, a novel ESCRT-III-related protein, associates with CHMP4b and functions in the endosomal sorting pathway

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia

Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis

Exome sequencing reveals VCP mutations as a cause of familial ALS

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

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Marka van Blitterswijk

Leonard H van den Berg

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2012-11-14T00:00:00Z

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233424488

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