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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

Papers overview

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2014
2007
2007
We isolated several senescence-associated genes (SAGs) from the petals of morning glory (Ipomoea nil) flowers, with the aim of… 
2007
2007
The authors studied inclusion formation in vitro using transiently transfected PC12 cells, with epitope-tagged and untagged full… 
2005
2005
Abstract: Two hereditary ataxia syndromes show distinct profiles of region‐specific atrophy and ocular motor deficits. Selective… 
Highly Cited
2003
Highly Cited
2003
Background: Hereditary motor and sensory neuropathy type 2C (HMSN2C, Charcot–Marie–Tooth 2C [CMT2C]) is an autosomal dominant… 
2002
2002
Spinocerebellar ataxia, type 2 (SCA2), results from an expansion of a stretch of polyglutamine repeats within the coding sequence… 
Highly Cited
2001
Highly Cited
2001
Expanded polyglutamine stretches have been shown to form aggregates and to be toxic to cells. In this study, we hypothesized that…