HAP1 can sequester a subset of TBP in cytoplasmic inclusions via specific interaction with the conserved TBP(CORE)

BACKGROUND: Huntington's disease, spinal and bulbar muscular atrophy, and spinocerebellar ataxia 17 (SCA17) are caused by expansions in the polyglutamine (polyQ) repeats in Huntingtin protein (Htt), androgen receptor protein (AR), and TATA-binding protein (TBP), respectively. Htt-associated pro...

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Detalles Bibliográficos
Autores principales: Prigge, Justin R, Schmidt, Edward E
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2082042/
https://www.ncbi.nlm.nih.gov/pubmed/17868456
http://dx.doi.org/10.1186/1471-2199-8-76

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2082042/
https://www.ncbi.nlm.nih.gov/pubmed/17868456
http://dx.doi.org/10.1186/1471-2199-8-76

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