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Published in 2020 at "Oxidative Medicine and Cellular Longevity"
DOI: 10.1155/2020/3129497
Abstract: Spinocerebellar ataxia type 17 (SCA17) is caused by a CAG/CAA expansion mutation encoding an expanded polyglutamine (polyQ) tract in TATA-box binding protein (TBP), a general transcription initiation factor. Suppression of cAMP-responsive element binding protein- (CREB-)…
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Keywords:
one 031;
hydroxy chromen;
ampk;
chromen one ... See more keywords
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Published in 2017 at "Journal of Neuroinflammation"
DOI: 10.1186/s12974-017-0925-3
Abstract: BackgroundPolyglutamine diseases constitute a class of neurodegenerative disorders associated with expansion of the cytosine-adenine-guanine (CAG) triplet, in protein coding genes. Expansion of a polyglutamine tract in the N-terminal of TBP is the causal mutation in…
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Keywords:
protein;
dysregulation;
polyglutamine;
binding protein ... See more keywords