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Ser46 phosphorylation and prolyl-isomerase Pin1-mediated isomerization of p53 are key events in p53-dependent apoptosis induced by mutant huntingtin

Huntington disease (HD) is a neurodegenerative disorder caused by a CAG repeat expansion in the gene coding for huntingtin protein. Several mechanisms have been proposed by which mutant huntingtin (mHtt) may trigger striatal neurodegeneration, including mitochondrial dysfunction, oxidative stress, a...

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Bibliografiske detaljer
Main Authors: Grison, Alice, Mantovani, Fiamma, Comel, Anna, Agostoni, Elena, Gustincich, Stefano, Persichetti, Francesca, Del Sal, Giannino
Format: Artigo
Sprog:Inglês
Udgivet: National Academy of Sciences 2011
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3207660/
https://ncbi.nlm.nih.gov/pubmed/22011578
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1106198108
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