Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals
about
Nuclear localization of the spinocerebellar ataxia type 7 protein, ataxin-7Huntingtin is ubiquitinated and interacts with a specific ubiquitin-conjugating enzymeHIP1, a human homologue of S. cerevisiae Sla2p, interacts with membrane-associated huntingtin in the brainPumilio1 haploinsufficiency leads to SCA1-like neurodegeneration by increasing wild-type Ataxin1 levelsAtaxin-1 with an expanded glutamine tract alters nuclear matrix-associated structuresInduction of endogenous genes following infection of human endothelial cells with an E1(-) E4(+) adenovirus gene transfer vectorPathogenic mechanisms of a polyglutamine-mediated neurodegenerative disease, spinocerebellar ataxia type 1Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1Gene, Stem Cell, and Alternative Therapies for SCA 1Cell biology of spinocerebellar ataxiaEvolutionary conservation and expression of human RNA-binding proteins and their role in human genetic diseasePolyglutamine expansion accelerates the dynamics of ataxin-1 and does not result in aggregate formation.Structural basis of protein complex formation and reconfiguration by polyglutamine disease protein Ataxin-1 and CapicuaExpansion, mosaicism and interruption: mechanisms of the CAG repeat mutation in spinocerebellar ataxia type 1Aberrant interactions of transcriptional repressor proteins with the Huntington's disease gene product, huntingtinThe cerebellar leucine-rich acidic nuclear protein interacts with ataxin-1SCA1-like disease in mice expressing wild-type ataxin-1 with a serine to aspartic acid replacement at residue 776.Reduction of glyceraldehyde-3-phosphate dehydrogenase activity in Alzheimer's disease and in Huntington's disease fibroblasts.RAS-MAPK-MSK1 pathway modulates ataxin 1 protein levels and toxicity in SCA1Autoregulation of Fox protein expression to produce dominant negative splicing factorsPolyglutamine pathogenesis.Progress in pathogenesis studies of spinocerebellar ataxia type 1.Spinocerebellar ataxia type 1--modeling the pathogenesis of a polyglutamine neurodegenerative disorder in transgenic mice.The molecular biology of the autosomal-dominant cerebellar ataxias.Impact of nuclear organization and dynamics on epigenetic regulation in the central nervous system: implications for neurological disease states.Expression of ataxin-2 in brains from normal individuals and patients with Alzheimer's disease and spinocerebellar ataxia 2.Broad distribution of ataxin 1 silencing in rhesus cerebella for spinocerebellar ataxia type 1 therapy.Stabilization and Degradation Mechanisms of Cytoplasmic Ataxin-1.The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects.Regulation of microRNA expression by HMGA1 proteins.Partial loss of Tip60 slows mid-stage neurodegeneration in a spinocerebellar ataxia type 1 (SCA1) mouse model.Cellular fusion for gene delivery to SCA1 affected Purkinje neurons.14-3-3 Binding to ataxin-1(ATXN1) regulates its dephosphorylation at Ser-776 and transport to the nucleus.Fusion of Human Fetal Mesenchymal Stem Cells with "Degenerating" Cerebellar Neurons in Spinocerebellar Ataxia Type 1 Model Mice.The importance of serine 776 in Ataxin-1 partner selection: a FRET analysis.Changes in Purkinje cell firing and gene expression precede behavioral pathology in a mouse model of SCA2Epigenetics in nucleotide repeat expansion disorders.Genetic and molecular aspects of spinocerebellar ataxias.Characterization of the zebrafish atxn1/axh gene family
P2860
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P2860
Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals
description
1995 nî lūn-bûn
@nan
1995 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Expression analysis of the ata ...... llar ataxia type 1 individuals
@ast
Expression analysis of the ata ...... llar ataxia type 1 individuals
@en
Expression analysis of the ata ...... llar ataxia type 1 individuals
@en-gb
Expression analysis of the ata ...... llar ataxia type 1 individuals
@nl
type
label
Expression analysis of the ata ...... llar ataxia type 1 individuals
@ast
Expression analysis of the ata ...... llar ataxia type 1 individuals
@en
Expression analysis of the ata ...... llar ataxia type 1 individuals
@en-gb
Expression analysis of the ata ...... llar ataxia type 1 individuals
@nl
prefLabel
Expression analysis of the ata ...... llar ataxia type 1 individuals
@ast
Expression analysis of the ata ...... llar ataxia type 1 individuals
@en
Expression analysis of the ata ...... llar ataxia type 1 individuals
@en-gb
Expression analysis of the ata ...... llar ataxia type 1 individuals
@nl
P2093
P3181
P356
P1433
P1476
Expression analysis of the ata ...... llar ataxia type 1 individuals
@en
P2093
P2888
P3181
P356
10.1038/NG0595-94
P407
P577
1995-05-01T00:00:00Z
P6179
1029169187