Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

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… Expand
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2017
Highly Cited
2017
Amyotrophic lateral sclerosis (ALS) is a rapidly progressing neurodegenerative disease that is characterized by motor neuron loss… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
Highly Cited
2014
Highly Cited
2014
Amyotrophic lateral sclerosis (ALS) is a fatal, late-onset neurodegenerative disease primarily affecting motor neurons. A… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
Review
2011
Review
2011
Local regulation of protein synthesis in neurons has emerged as a leading research focus because of its importance in synaptic… Expand
  • figure 1
Is this relevant?
Highly Cited
2007
Highly Cited
2007
Tight control of translation is fundamental for eukaryotic cells, and deregulation of proteins implicated contributes to numerous… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
Highly Cited
2007
Highly Cited
2007
Cytogenetic imbalances are increasingly being realized as causes of autism. Here, we report a de novo translocation between the… Expand
Is this relevant?
Highly Cited
2001
Highly Cited
2001
We have determined the solution structure of the C-terminal quarter of human poly(A)-binding protein (hPABP). The protein… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
Highly Cited
2000
Highly Cited
2000
Instability of CAG DNA trinucleotide repeats is the mutational mechanism for several neurodegenerative diseases resulting in the… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
Highly Cited
2000
Highly Cited
2000
Spinocerebellar ataxia type 2 (SCA2) is caused by expansion of a polyglutamine tract in ataxin-2, a protein of unknown function… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
Highly Cited
1999
Highly Cited
1999
Spinocerebellar ataxia type 2 (SCA2) is caused by expansion of a CAG trinucleotide repeat located in the coding region of the… Expand
Is this relevant?
Highly Cited
1997
Highly Cited
1997
The dominant cerebellar ataxias (ADCAs) represent a clinically and genetically heterogeneous group of disorders linked by… Expand
Is this relevant?