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Poly-glutamine expanded huntingtin dramatically alters the genome wide binding of HSF1

In Huntington’s disease (HD), polyglutamine expansions in the huntingtin (Htt) protein cause subtle changes in cellular functions that, over-time, lead to neurodegeneration and death. Studies have indicated that activation of the heat shock response can reduce many of the effects of mutant Htt in di...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Riva, Laura, Koeva, Martina, Yildirim, Ferah, Pirhaji, Leila, Dinesh, Deepika, Mazor, Tali, Duennwald, Martin L., Fraenkel, Ernest
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2012
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3537492/
https://ncbi.nlm.nih.gov/pubmed/23293686
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