ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19
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Genotype-phenotype correlations of amyotrophic lateral sclerosisClinical and genetic basis of familial amyotrophic lateral sclerosisALS as a distal axonopathy: molecular mechanisms affecting neuromuscular junction stability in the presymptomatic stages of the diseaseTargeted exon capture and sequencing in sporadic amyotrophic lateral sclerosis.Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS.Significant expansion of the REST/NRSF cistrome in human versus mouse embryonic stem cells: potential implications for neural developmentGenotype-phenotype relationship in hereditary amyotrophic lateral sclerosis.Dysregulated expression of death, stress and mitochondrion related genes in the sciatic nerve of presymptomatic SOD1(G93A) mouse model of Amyotrophic Lateral Sclerosis.Neuregulin 1 confers neuroprotection in SOD1-linked amyotrophic lateral sclerosis mice via restoration of C-boutons of spinal motor neurons.A(a)LS: Ammonia-induced amyotrophic lateral sclerosis.Rare variants analysis of cutaneous malignant melanoma genes in Parkinson's disease.Neuregulin 1-ErbB module in C-bouton synapses on somatic motor neurons: molecular compartmentation and response to peripheral nerve injury.Epidemiology and molecular mechanism of frontotemporal lobar degeneration/amyotrophic lateral sclerosis with repeat expansion mutation in C9orf72.CACNA1H missense mutations associated with amyotrophic lateral sclerosis alter Cav3.2 T-type calcium channel activity and reticular thalamic neuron firing.Activating ERBB4 mutations in non-small cell lung cancer.TDP-43 loss of function inhibits endosomal trafficking and alters trophic signaling in neurons.Neuromuscular Junction Dismantling in Amyotrophic Lateral Sclerosis.The evolving genetic risk for sporadic ALS.Sigma-1 Receptor in Motoneuron Disease.Neuregulin 1 Reduces Motoneuron Cell Death and Promotes Neurite Growth in an in Vitro Model of Motoneuron Degeneration.Detection of an interaction between prion protein and neuregulin I-β1 by fluorescence resonance energy transfer analysis.TDP-43 gains function due to perturbed autoregulation in a Tardbp knock-in mouse model of ALS-FTD.Familial Amyotrophic Lateral Sclerosis.Dysfunction of Optineurin in Amyotrophic Lateral Sclerosis and Glaucoma.Amyotrophic lateral sclerosis
P2860
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P2860
ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19
description
2013 nî lūn-bûn
@nan
2013 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
ERBB4 mutations that disrupt t ...... phic lateral sclerosis type 19
@ast
ERBB4 mutations that disrupt t ...... phic lateral sclerosis type 19
@en
ERBB4 mutations that disrupt t ...... phic lateral sclerosis type 19
@nl
type
label
ERBB4 mutations that disrupt t ...... phic lateral sclerosis type 19
@ast
ERBB4 mutations that disrupt t ...... phic lateral sclerosis type 19
@en
ERBB4 mutations that disrupt t ...... phic lateral sclerosis type 19
@nl
prefLabel
ERBB4 mutations that disrupt t ...... phic lateral sclerosis type 19
@ast
ERBB4 mutations that disrupt t ...... phic lateral sclerosis type 19
@en
ERBB4 mutations that disrupt t ...... phic lateral sclerosis type 19
@nl
P2093
P2860
P50
P3181
P1476
ERBB4 mutations that disrupt t ...... phic lateral sclerosis type 19
@en
P2093
Asao Fujiyama
Atsushi Toyoda
Budrul Ahsan
Fumiharu Kimura
Garth A Nicholson
Hidetoshi Date
Hiroyoko Moritoyo
Hiroyuki Ishiura
Ian P Blair
P2860
P3181
P356
10.1016/J.AJHG.2013.09.008
P407
P50
P577
2013-11-07T00:00:00Z