Regional rescue of spinocerebellar ataxia type 1 phenotypes by 14-3-3epsilon haploinsufficiency in mice underscores complex pathogenicity in neurodegeneration
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Cell biology of spinocerebellar ataxiaMouse models of polyglutamine diseases: review and data table. Part IMouse models of polyglutamine diseases in therapeutic approaches: review and data table. Part II.Beyond the glutamine expansion: influence of posttranslational modifications of ataxin-1 in the pathogenesis of spinocerebellar ataxia type 1Polyglutamine neurodegeneration: expanded glutamines enhance native functionsRAS-MAPK-MSK1 pathway modulates ataxin 1 protein levels and toxicity in SCA1Broad therapeutic benefit after RNAi expression vector delivery to deep cerebellar nuclei: implications for spinocerebellar ataxia type 1 therapyStabilization and Degradation Mechanisms of Cytoplasmic Ataxin-1.Differential effects of delayed aging on phenotype and striatal pathology in a murine model of Huntington disease.Evolution and function of CAG/polyglutamine repeats in protein-protein interaction networks.Polyglutamine disease toxicity is regulated by Nemo-like kinase in spinocerebellar ataxia type 1.Genetically engineered mouse models of the trinucleotide-repeat spinocerebellar ataxias.Huntington's disease and the striatal medium spiny neuron: cell-autonomous and non-cell-autonomous mechanisms of diseaseNeuroprotective function of 14-3-3 proteins in neurodegenerationFrom pathways to targets: understanding the mechanisms behind polyglutamine disease.Cerebellar Transcriptome Profiles of ATXN1 Transgenic Mice Reveal SCA1 Disease Progression and Protection Pathways.14-3-3 Proteins in the regulation of rotenone-induced neurotoxicity might be via its isoform 14-3-3epsilon's involvement in autophagy.Extensive cryptic splicing upon loss of RBM17 and TDP43 in neurodegeneration models.Motor neuron degeneration correlates with respiratory dysfunction in SCA1.PAK1 regulates ATXN1 levels providing an opportunity to modify its toxicity in Spinocerebellar ataxia type 1.
P2860
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P2860
Regional rescue of spinocerebellar ataxia type 1 phenotypes by 14-3-3epsilon haploinsufficiency in mice underscores complex pathogenicity in neurodegeneration
description
2011 nî lūn-bûn
@nan
2011 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2011年の論文
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2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Regional rescue of spinocerebe ...... ogenicity in neurodegeneration
@ast
Regional rescue of spinocerebe ...... ogenicity in neurodegeneration
@en
Regional rescue of spinocerebe ...... ogenicity in neurodegeneration
@nl
type
label
Regional rescue of spinocerebe ...... ogenicity in neurodegeneration
@ast
Regional rescue of spinocerebe ...... ogenicity in neurodegeneration
@en
Regional rescue of spinocerebe ...... ogenicity in neurodegeneration
@nl
prefLabel
Regional rescue of spinocerebe ...... ogenicity in neurodegeneration
@ast
Regional rescue of spinocerebe ...... ogenicity in neurodegeneration
@en
Regional rescue of spinocerebe ...... ogenicity in neurodegeneration
@nl
P2860
P50
P356
P1476
Regional rescue of spinocerebe ...... ogenicity in neurodegeneration
@en
P2093
Paymaan Jafar-Nejad
Ronald Richman
P2860
P304
P356
10.1073/PNAS.1018748108
P407
P577
2011-01-18T00:00:00Z