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Opposing effects of polyglutamine expansion on native protein complexes contribute to SCA1

Spinocerebellar ataxia type 1 (SCA1) is a dominantly inherited neurodegenerative disease caused by expansion of a glutamine-encoding repeat in SCA1. In all known polyglutamine diseases, the glutamine expansion confers toxic functions onto the protein. The mechanism by which this occurs remains enigm...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Lim, Janghoo, Crespo-Barreto, Juan, Jafar-Nejad, Paymaan, Bowman, Aaron B., Richman, Ronald, Hill, David E., Orr, Harry T., Zoghbi, Huda Y.
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: 2008
Θέματα:
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2377396/
https://ncbi.nlm.nih.gov/pubmed/18337722
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nature06731
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