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ATXN2 protein, human

Known as: ataxin-2 protein, human, Spinocerebellar Ataxia Type 2 Protein, ATX2 protein, human 
Ataxin-2 (1313 aa, ~140 kDa) is encoded by the human ATXN2 gene. This protein plays a role in the modulation of epidermal growth factor receptor… 
National Institutes of Health

Related topics

Related topics

9 relations
ATXN2 geneCellular MembraneCytoplasmLigand Binding

Broader (1)

Ataxin-2

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2018
Review
2018
Cytoplasmic RNA granules, ribostasis, and neurodegeneration
The regulation of translation and decay of messenger RNA (mRNA) is a key mechanism for control of gene expression. During… 
2016
2016
El polimorfismo (CAG)n del gen ATXN2, nuevo marcador de susceptibilidad para diabetes mellitus tipo 2
RESUMEN Objetivo Estimar si hay asociacion del repetido (CAG)n del gen ATXN2 en poblacion mexicana con diabetes mellitus (DM… 
2015
2015
Autophagy manages disease-associated stress granules
Abnormal accumulation of cytosolic aggregates or inclusion bodies is a hallmark of several neurodegenerative diseases. Many… 
2014
2014
Neuropathological Staging of Spinocerebellar Ataxia Type 2 by Semiquantitative 1C2‐Positive Neuron Typing. Nuclear Translocation of Cytoplasmic 1C2 Underlies Disease Progression of Spinocerebellar…
Spinocerebellar ataxia type 2 (SCA2) is a hereditary neurodegenerative disorder caused by the expansion of the trinucleotide CAG… 
2008
2008
[Molecular analysis of the CAG repeat among patients with Type-2 spinocerebellar ataxia in the Mexican population].
BACKGROUND Spinocerebellar ataxia type 2 (SCA2) results from the expansion of a CAG triplet located within the coding sequence of… 
2007
2007
INCLUSION FORMATION BY ATAXINS -1, -2, -3, AND -7
The authors studied inclusion formation in vitro using transiently transfected PC12 cells, with epitope-tagged and untagged full… 
2005
2005
Partial resistance of ataxin-2-containing olivary and pontine neurons to axotomy-induced degeneration
2004
2004
Can ataxin-2 be down-regulated by allele-specific de novo DNA methylation in SCA2 patients?
Highly Cited
2003
Highly Cited
2003
The gene for HMSN2C maps to 12q23-24
Background: Hereditary motor and sensory neuropathy type 2C (HMSN2C, Charcot–Marie–Tooth 2C [CMT2C]) is an autosomal dominant… 
2002
2002
Accurate determination of ataxin-2 polyglutamine expansion in patients with intermediate-range repeats.
Spinocerebellar ataxia, type 2 (SCA2), results from an expansion of a stretch of polyglutamine repeats within the coding sequence… 
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