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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Détails bibliographiques
Auteurs principaux: S.Y. Cong, B.A. Pepers, T.T. Zhou, H. Kerkdijk, R.A. Roos, G.J. van Ommen, J.C. Dorsman
Format: Article
Langue:English
Publié: Elsevier 2012-06-01
Collection:Neurobiology of Disease
Sujets:
Accès en ligne:http://www.sciencedirect.com/science/article/pii/S0969996112000794