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Targeting the UPR transcription factor XBP1 protects against Huntington's disease through the regulation of FoxO1 and autophagy

Mutations leading to expansion of a poly-glutamine track in Huntingtin (Htt) cause Huntington's disease (HD). Signs of endoplasmic reticulum (ER) stress have been recently reported in animal models of HD, associated with the activation of the unfolded protein response (UPR). Here we have invest...

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Dettagli Bibliografici
Autori principali: Vidal, Rene L., Figueroa, Alicia, Court, Felipe A., Thielen, Peter, Molina, Claudia, Wirth, Craig, Caballero, Benjamin, Kiffin, Roberta, Segura-Aguilar, Juan, Cuervo, Ana Maria, Glimcher, Laurie H., Hetz, Claudio
Natura: Artigo
Lingua:Inglês
Pubblicazione: Oxford University Press 2012
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3335312/
https://ncbi.nlm.nih.gov/pubmed/22337954
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/dds040
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