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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Бібліографічні деталі
Автори: S.Y. Cong, B.A. Pepers, T.T. Zhou, H. Kerkdijk, R.A. Roos, G.J. van Ommen, J.C. Dorsman
Формат: Стаття
Мова:English
Опубліковано: Elsevier 2012-06-01
Серія:Neurobiology of Disease
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Онлайн доступ:http://www.sciencedirect.com/science/article/pii/S0969996112000794