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Mitochondrial and redox modifications in early stages of Huntington's disease

Deficits in mitochondrial function and redox deregulation have been attributed to Huntington's disease (HD), a genetic neurodegenerative disorder largely affecting the striatum. However, whether these changes occur in early stages of the disease and can be detected in vivo is still unclear. In...

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Detalles Bibliográficos
Autores principales:	Lopes, Carla, Ferreira, I. Luísa, Maranga, Carina, Beatriz, Margarida, Mota, Sandra I., Sereno, José, Castelhano, João, Abrunhosa, Antero, Oliveira, Francisco, De Rosa, Maura, Hayden, Michael, Laço, Mário N., Januário, Cristina, Castelo Branco, Miguel, Rego, A. Cristina
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2022
Materias:	Research Paper
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9420526/ https://www.ncbi.nlm.nih.gov/pubmed/35988447 http://dx.doi.org/10.1016/j.redox.2022.102424

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