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Ataxins

Known as: Proteins, Spinocerebellar Ataxia, Ataxin Proteins, Spinocerebellar Ataxia Proteins 
A family of predominantly nuclear proteins that regulate gene transcription and protein degradation. The expansion of CAG trinucleotide repeats in… 
National Institutes of Health

Papers overview

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Review
2010
Review
2010
Huntington’s disease (HD) and spinocerebellar ataxias (SCAs) are autosomal-dominant neurodegenerative disorders. HD is caused by… 
Review
2010
Review
2010
A number of neurodegenerative diseases, including Alzheimer's disease, tauopathies, Parkinson's disease, and synucleinopathies… 
Highly Cited
2008
Highly Cited
2008
Highly Cited
2003
Highly Cited
2003
The spinocerebellar ataxias (SCAs) are a class of hereditary neurodegenerative diseases, which are caused by the pathological… 
2003
2003
The deposition of abnormal protein fibrils is a prominent pathological feature of many different ‘protein conformational… 
Review
2000
Review
2000
  • G. Morris
  • Neuromuscular Disorders
  • 2000
  • Corpus ID: 45280542
1995
1995
  • R. Rosenberg
  • The New England journal of medicine
  • 1995
  • Corpus ID: 41455215
Neurology textbooks are replete with descriptions of clinical syndromes of ataxia due to various forms of spinocerebellar…