Maintenance of basal levels of autophagy in Huntington's disease mouse models displaying metabolic dysfunction.
Huntington's disease (HD) is a fatal neurodegenerative disorder caused by an expanded polyglutamine repeat in the huntingtin protein. Neuropathology in the basal ganglia and in the cerebral cortex has been linked to the motor and cognitive symptoms whereas recent work has suggested that the hyp...
Enregistré dans:
Auteurs principaux: | Barbara Baldo, Rana Soylu, Asa Petersén |
---|---|
Format: | article |
Langue: | EN |
Publié: |
Public Library of Science (PLoS)
2013
|
Sujets: | |
Accès en ligne: | https://doaj.org/article/5f193679e8fa4998bc8932e1e76bb743 |
Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
Documents similaires
-
Sexually dimorphic serotonergic dysfunction in a mouse model of Huntington's disease and depression.
par: Thibault Renoir, et autres
Publié: (2011) -
Objective acoustic quantification of phonatory dysfunction in Huntington's disease.
par: Jan Rusz, et autres
Publié: (2013) -
D-β-hydroxybutyrate is protective in mouse models of Huntington's disease.
par: Soyeon Lim, et autres
Publié: (2011) -
Global Rhes knockout in the Q175 Huntington's disease mouse model.
par: Taneli Heikkinen, et autres
Publié: (2021) -
Deubiquitinase Usp12 functions noncatalytically to induce autophagy and confer neuroprotection in models of Huntington’s disease
par: Rebecca Aron, et autres
Publié: (2018)