Preventing mutant huntingtin proteolysis and intermittent fasting promote autophagy in models of Huntington disease

Huntington disease (HD) is caused by the expression of mutant huntingtin (mHTT) bearing a polyglutamine expansion. In HD, mHTT accumulation is accompanied by a dysfunction in basal autophagy, which manifests as specific defects in cargo loading during selective autophagy. Here we show that the expre...

Full beskrivning

Sparad:
Bibliografiska uppgifter
I publikationen:Acta Neuropathol Commun
Huvudupphovsmän: Ehrnhoefer, Dagmar E., Martin, Dale D. O., Schmidt, Mandi E., Qiu, Xiaofan, Ladha, Safia, Caron, Nicholas S., Skotte, Niels H., Nguyen, Yen T. N., Vaid, Kuljeet, Southwell, Amber L., Engemann, Sabine, Franciosi, Sonia, Hayden, Michael R.
Materialtyp: Artigo
Språk:Inglês
Publicerad: BioMed Central 2018
Ämnen:
Research
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC5839066/
https://ncbi.nlm.nih.gov/pubmed/29510748
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40478-018-0518-0
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!

Liknande verk