Skip to search formSkip to main contentSkip to account menu

ATXN10 gene

Known as: E46L, ATXN10, E46-LIKE 
National Institutes of Health

Related topics

Related topics

1 relation
Spinocerebellar Ataxia 10

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
ATXN10 Microsatellite Distribution in a Peruvian Amerindian Population
Spinocerebellar ataxia type 10 (SCA10) is a repeat expansion disease occurring mostly in Latin America, suggesting that the… 
2013
2013
An interaction between the methyltransferase and RNA dependent RNA polymerase domains of the West Nile virus NS5 protein.
The flavivirus nonstructural protein 5 (NS5) is a large protein that is structurally conserved among members of the genus, making… 
2013
2013
An interaction between the methyltransferase and RNA dependent RNA polymerase 1 domains of the West Nile virus NS 5 protein 2 Running title : An interaction between the WNV NS 5 MTase-POL 3
Highly Cited
2010
Highly Cited
2010
Inactivation of hnRNP K by Expanded Intronic AUUCU Repeat Induces Apoptosis Via Translocation of PKCδ to Mitochondria in Spinocerebellar Ataxia 10
We have identified a large expansion of an ATTCT repeat within intron 9 of ATXN10 on chromosome 22q13.31 as the genetic mutation… 
Review
2008
Review
2008
Recent progress in spinocerebellar ataxia type-10 (SCA10)
Spinocerebellar ataxia type 10 (SCA10) is a dominantly inherited ataxia caused by expansion of ATTCT pentanucleotide repeat in… 
Highly Cited
2007
Highly Cited
2007
Unstable Spinocerebellar Ataxia Type 10 (ATTCT)·(AGAAT) Repeats Are Associated with Aberrant Replication at the ATX10 Locus and Replication Origin-Dependent Expansion at an Ectopic Site in Human…
ABSTRACT Spinocerebellar ataxia type 10 (SCA10) is associated with expansion of (ATTCT)n repeats (where n is the number of… 
Highly Cited
2006
Highly Cited
2006
The role of ataxin 10 in the pathogenesis of spinocerebellar ataxia type 10
Background: Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant disorder characterized by cerebellar ataxia and… 
2006
2006
Ataxin 10 induces neuritogenesis via interaction with G‐protein β2 subunit
Spinocerebellar ataxia type 10 (SCA10) is a dominantly inherited disorder caused by an intronic ATTCT pentanucleotide repeat… 
Review
2001
Review
2001
[Spinocerebellar ataxia type 10 (SCA10): a disease caused by a novel pentanucleotide repeat expansion].
Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant progressive disorder characterized by ataxia, seizures and… 
1993
1993
Modification of the head-group selectivity of porcine pancreatic phospholipase A2 by protein engineering.
On the basis of the three-dimensional structures of phospholipid and porcine pancreatic phospholipase A2 (pla2), it was predicted… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)