Brain Region and Cell Compartment Dependent Regulation of Electron Transport System Components in Huntington’s Disease Model Mice

Huntington’s disease (HD) is a rare hereditary neurodegenerative disorder characterized by multiple metabolic dysfunctions including defects in mitochondrial homeostasis and functions. Although we have recently reported age-related changes in the respiratory capacities in different brain areas in HD...

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Detalhes bibliográficos

Principais autores:	Johannes Burtscher, Giuseppe Pepe, Federico Marracino, Luca Capocci, Susy Giova, Grégoire P. Millet, Alba Di Pardo, Vittorio Maglione
Formato:	Artigo
Idioma:	Inglês
Publicado em:	MDPI AG 2021-09-01
coleção:	Brain Sciences
Assuntos:	Huntington’s disease mitochondria oxidative phosphorylation neurodegeneration striatum cortex
Acesso em linha:	https://www.mdpi.com/2076-3425/11/10/1267
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