Effects of Pin1 Loss in Hdh(Q111) Knock-in Mice

Huntington’s disease (HD) is a fatal, dominantly inherited, neurodegenerative disorder due to a pathological expansion of the CAG repeat in the coding region of the HTT gene. In the quest for understanding the molecular basis of neurodegeneration, we have previously demonstrated that the prolyl isom...

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發表在:Front Cell Neurosci
Main Authors: Agostoni, Elena, Michelazzi, Silvia, Maurutto, Marta, Carnemolla, Alisia, Ciani, Yari, Vatta, Paolo, Roncaglia, Paola, Zucchelli, Silvia, Leanza, Giampiero, Mantovani, Fiamma, Gustincich, Stefano, Santoro, Claudio, Piazza, Silvano, Del Sal, Giannino, Persichetti, Francesca
格式: Artigo
語言:Inglês
出版: Frontiers Media S.A. 2016
主題:
Neuroscience
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC4852193/
https://ncbi.nlm.nih.gov/pubmed/27199664
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fncel.2016.00110
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