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ATXN8OS gene

Known as: ATAXIN 8 OPPOSITE STRAND, SCA8, ATXN8 opposite strand (non-protein coding) 
National Institutes of Health

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SPINOCEREBELLAR ATAXIA 8

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Biological function of long noncoding RNA snaR in HER2-positive breast cancer cells
Purpose: Long noncoding RNA, snaR (small NF90-associated RNA), has been reported to be upregulated in various cancer cell lines… 
Review
2005
Review
2005
Adult Onset Spinocerebellar Ataxia in a Canadian Movement Disorders Clinic
ABSTRACT: Background: The spinocerebellar ataxias (SCAs) are a genetically and clinically heterogeneous group of… 
2005
2005
Giant SCA8 alleles in nine children whose mother has two moderately large ones
We report here a family in which each of nine children has inherited giant SCA8 CTG expansions from a homozygous mother who has… 
2005
2005
Frequency analysis of autosomal dominant spinocerebellar ataxias in mainland Chinese patients and clinical and molecular characterization of spinocerebellar ataxia type 6.
BACKGROUND Dominantly inherited spinocerebellar ataxia (SCA) is a clinically and genetically heterogeneous group of… 
2004
2004
Polymorphism of trinucleotide repeats in non-translated regions of SCA8 and SCA12 genes: allele distribution in a Polish control group.
Spinocerebellar ataxias are a group of neurodegenerative disorders caused by dynamic mutations of microsatellite repeats. Two… 
Highly Cited
2003
Highly Cited
2003
A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23.
The autosomal dominant cerebellar ataxias (ADCA) are a clinically, pathologically and genetically heterogeneous group of… 
2002
2002
The KLHL1-antisense transcript ( KLHL1AS) is evolutionarily conserved.
Spinocerebellar ataxia type 8 (SCA8) is caused by a CTG expansion in an untranslated, endogenous antisense RNA that overlaps the… 
2002
2002
SCA8 in the Spanish population including one homozygous patient
Controversial data have been reported about SCA8 since its description in 1999. The most accepted hypothesis is that CTG… 
2002
2002
Calculating predictive values for the large repeat alleles at the SCA8 locus in patients with ataxia
Since the original description of SCA8 in 1999,1 several reports have been published on the occurrence of the SCA8 gene CTG… 
2001
2001
Frequency analysis of autosomal dominant cerebellar ataxias in Taiwanese patients and clinical and molecular characterization of spinocerebellar ataxia type 6.
BACKGROUND Spinocerebellar ataxia (SCA) is a heterogeneous group of neurodegenerative disorders. The mutational basis for most of… 
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