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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Dettagli Bibliografici
Autori principali: S.Y. Cong, B.A. Pepers, T.T. Zhou, H. Kerkdijk, R.A. Roos, G.J. van Ommen, J.C. Dorsman
Natura: Articolo
Lingua:English
Pubblicazione: Elsevier 2012-06-01
Serie:Neurobiology of Disease
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Accesso online:http://www.sciencedirect.com/science/article/pii/S0969996112000794