Genetic overlap between apparently sporadic motor neuron diseases.
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Genotype-phenotype correlations of amyotrophic lateral sclerosisNeuropathology 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 CHMP2BRab8, POSH, and TAK1 regulate synaptic growth in a Drosophila model of frontotemporal dementiaControversies 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 factorThe El Escorial criteria: Strengths and weaknessesTime to generalization and prediction of survival in patients with amyotrophic lateral sclerosis: a retrospective observational studyClinical variability and additional mutations in amyotrophic lateral sclerosis patients with p.N352S mutations inTARDBP
P2860
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P2860
Genetic overlap between apparently sporadic motor neuron diseases.
description
2012 nî lūn-bûn
@nan
2012 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
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
P2093
P2860
P50
P1433
P1476
Genetic overlap between apparently sporadic motor neuron diseases.
@en
P2093
Anneke J van der Kooi
Dennis Dooijes
Eric A M Hennekam
Helenius J Schelhaas
Lotte Vlam
Marianne de Visser
Michael A van Es
W-Ludo van der Pol
P2860
P304
P356
10.1371/JOURNAL.PONE.0048983
P407
P577
2012-11-14T00:00:00Z