ATXN1 gene

Known as: D6S504E, ATX1, ATXN1 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1999-2018
024619992018

Papers overview

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2012
2012
Interstitial deletions of the short arm of chromosome 6 are rare and have been associated with developmental delay, hypotonia… (More)
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2011
2011
Although expansion of CAG repeats in ATAXIN1 (ATXN1) causes Spinocerebellar ataxia type 1, the functions of ATXN1 and ATAXIN1… (More)
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2011
2011
Ataxin-1 (ATXN1), a causative factor for spinocerebellar ataxia type 1 (SCA1), and the related Brother of ATXN1 (BOAT1) are human… (More)
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2011
2011
Spinocerebellar ataxia type 1 (SCA1) is a lethal neurodegenerative disorder caused by expansion of a polyglutamine tract in ATXN1… (More)
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2010
2010
Alzheimer disease (AD) is a devastating neurodegenerative disease with complex and strong genetic inheritance. Four genes have… (More)
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2010
2010
Spinocerebellar ataxia type 1 (SCA1) is a dominantly inherited neurodegenerative disease caused by expansion of a CAG repeat that… (More)
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Highly Cited
2008
Highly Cited
2008
Spinocerebellar ataxia type 1 is caused by expansion of a translated CAG repeat in ataxin1 (ATXN1). The level of the… (More)
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2007
2007
BACKGROUND Multiple system atrophy (MSA) has been considered a sporadic disease, without patterns of inheritance. OBJECTIVE To… (More)
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2006
2006
The Arabidopsis homolog of trithorax, ATX1, regulates numerous functions in Arabidopsis beyond the homeotic genes. Here, we… (More)
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Highly Cited
2006
Highly Cited
2006
Spinocerebellar ataxia type 1 (SCA1) is one of several neurodegenerative diseases caused by expansion of a polyglutamine tract in… (More)
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