TDP-43 expression in mouse models of amyotrophic lateral sclerosis and spinal muscular atrophy.
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A comprehensive assessment of the SOD1G93A low-copy transgenic mouse, which models human amyotrophic lateral sclerosis.Neuropathology of Amyotrophic Lateral Sclerosis and Its Variants.Altered nucleocytoplasmic proteome and transcriptome distributions in an in vitro model of amyotrophic lateral sclerosisMitochondrial dysfunction and decrease in body weight of a transgenic knock-in mouse model for TDP-43.Presynaptic localization of Smn and hnRNP R in axon terminals of embryonic and postnatal mouse motoneuronsDiacetylbis(N(4)-methylthiosemicarbazonato) copper(II) (CuII(atsm)) protects against peroxynitrite-induced nitrosative damage and prolongs survival in amyotrophic lateral sclerosis mouse model.Molecular neuropathology of TDP-43 proteinopathies.The Overexpression of TDP-43 Protein in the Neuron and Oligodendrocyte Cells Causes the Progressive Motor Neuron Degeneration in the SOD1 G93A Transgenic Mouse Model of Amyotrophic Lateral SclerosisFunctional recovery in new mouse models of ALS/FTLD after clearance of pathological cytoplasmic TDP-43.Overexpression of survival motor neuron improves neuromuscular function and motor neuron survival in mutant SOD1 mice.TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration.Emerging drugs for amyotrophic lateral sclerosis.Magnetic resonance imaging of pathological processes in rodent models of amyotrophic lateral sclerosis.Gem depletion: amyotrophic lateral sclerosis and spinal muscular atrophy crossover.Frontotemporal lobar degeneration: Pathogenesis, pathology and pathways to phenotype.Cajal bodies in neuronsThe JNK/c-Jun signaling axis contributes to the TDP-43-induced cell death.Intrathecal infusion of BMAA induces selective motor neuron damage and astrogliosis in the ventral horn of the spinal cord.Early and selective reduction of NOP56 (Asidan) and RNA processing proteins in the motor neuron of ALS model mice.Differential expression of TAR DNA-binding protein (TDP-43) in the central nervous system of horses afflicted with equine motor neuron disease (EMND): a preliminary study of a potential pathologic marker.
P2860
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P2860
TDP-43 expression in mouse models of amyotrophic lateral sclerosis and spinal muscular atrophy.
description
2008 nî lūn-bûn
@nan
2008 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
name
TDP-43 expression in mouse mod ...... s and spinal muscular atrophy.
@ast
TDP-43 expression in mouse mod ...... s and spinal muscular atrophy.
@en
type
label
TDP-43 expression in mouse mod ...... s and spinal muscular atrophy.
@ast
TDP-43 expression in mouse mod ...... s and spinal muscular atrophy.
@en
prefLabel
TDP-43 expression in mouse mod ...... s and spinal muscular atrophy.
@ast
TDP-43 expression in mouse mod ...... s and spinal muscular atrophy.
@en
P2093
P2860
P356
P1433
P1476
TDP-43 expression in mouse mod ...... s and spinal muscular atrophy.
@en
P2093
Dirk Bäumer
Jakub Scaber
Nicholas J Parkinson
Olaf Ansorge
P2860
P2888
P356
10.1186/1471-2202-9-104
P577
2008-10-28T00:00:00Z
P5875
P6179
1005447167