Pterostilbene in Combination With Mitochondrial Cofactors Improve Mitochondrial Function in Cellular Models of Mitochondrial Diseases

Mitochondrial diseases are genetic disorders caused by mutations in genes in the nuclear DNA (nDNA) and mitochondrial DNA (mtDNA) that encode mitochondrial structural or functional proteins. Although considered “rare” due to their low incidence, such diseases affect thousands of patients’ lives worl...

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Principais autores:	Juan M. Suárez-Rivero, Carmen J. Pastor-Maldonado, Ana Romero-González, David Gómez-Fernandez, Suleva Povea-Cabello, Mónica Álvarez-Córdoba, Irene Villalón-García, Marta Talaverón-Rey, Alejandra Suárez-Carrillo, Manuel Munuera-Cabeza, José A. Sánchez-Alcázar
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Frontiers Media S.A. 2022-03-01
coleção:	Frontiers in Pharmacology
Assuntos:	pterostilbene sirt3 UPRmt mitochondrial diseases mitochondrial cofactors
Acesso em linha:	https://www.frontiersin.org/articles/10.3389/fphar.2022.862085/full
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