Huntingtin with an expanded polyglutamine repeat affects the Jab1-p27(Kip1) pathway

Expansion of polyglutamine repeats is the cause of at least nine inherited human neurodegenerative disorders, including Huntington's disease (HD). It is widely accepted that deregulation of the transcriptional coactivator CBP by expanded huntingtin (htt) plays an important role in HD molecular...

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Библиографические подробности
Главные авторы: S.Y. Cong, B.A. Pepers, T.T. Zhou, H. Kerkdijk, R.A. Roos, G.J. van Ommen, J.C. Dorsman
Формат: Статья
Язык:English
Опубликовано: Elsevier 2012-06-01
Серии:Neurobiology of Disease
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Online-ссылка:http://www.sciencedirect.com/science/article/pii/S0969996112000794