Carregant...

Oxidative metabolism and Ca(2+) handling in striatal mitochondria from YAC128 mice, a model of Huntington’s disease

The mechanisms implicated in the pathology of Huntington’s disease (HD) remain not completely understood, although dysfunction of mitochondrial oxidative metabolism and Ca(2+) handling have been suggested as contributing factors. However, in our previous studies with mitochondria isolated from the w...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Neurochem Int
Autors principals: Hamilton, James, Brustovetsky, Tatiana, Brustovetsky, Nickolay
Format: Artigo
Idioma:Inglês
Publicat: 2017
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5495615/
https://ncbi.nlm.nih.gov/pubmed/28062223
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuint.2017.01.001
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!