Ataxin-7

Known as: Ataxin-7 [Chemical/Ingredient], Atxn 7 Protein, Spinocerebellar Ataxia 7 Protein 
A component of the STAGA transcription coactivator-HAT complex that functions in Cone Rod Homeobox Protein (CRX)-dependent gene activation. It also… (More)
National Institutes of Health

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Highly Cited
2011
Highly Cited
2011
Spinocerebellar ataxia type 7 (SCA7) is a neurodegenerative disorder caused by CAG/polyglutamine repeat expansions in the ataxin… (More)
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Highly Cited
2008
Highly Cited
2008
Targeting of a gene to the nuclear pore complexes (NPCs), known as gene gating, can affect its transcriptional state. However… (More)
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Highly Cited
2006
Highly Cited
2006
Non-neuronal cells may be pivotal in neurodegenerative disease, but the mechanistic basis of this effect remains ill-defined. In… (More)
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Highly Cited
2006
Highly Cited
2006
Spinocerebellar ataxia type 7 (SCA7) is one of several inherited neurodegenerative disorders caused by a polyglutamine (polyQ… (More)
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Highly Cited
2005
Highly Cited
2005
Spinocerebellar ataxia type 7 (SCA7) is characterized by cone-rod dystrophy retinal degeneration and is caused by a polyglutamine… (More)
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Highly Cited
2004
Highly Cited
2004
Spinocerebellar ataxia type 7 (SCA7) is a neurodegenerative disorder caused by a CAG repeat expansion in the SCA7 gene leading to… (More)
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Highly Cited
2003
Highly Cited
2003
We targeted 266 CAG repeats (a number that causes infantile-onset disease) into the mouse Sca7 locus to generate an authentic… (More)
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Highly Cited
2003
Highly Cited
2003
The spinocerebellar ataxias (SCAs) are a class of hereditary neurodegenerative diseases, which are caused by the pathological… (More)
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Highly Cited
2002
Highly Cited
2002
Spinocerebellar ataxia (SCA) type 7 is an inherited neurodegenerative disorder caused by expansion of a polyglutamine tract… (More)
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Highly Cited
2001
Highly Cited
2001
Spinocerebellar ataxia type 7 (SCA7) is an autosomal dominant disorder caused by a CAG repeat expansion. To determine the… (More)
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