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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Detalles Bibliográficos
Autores principales: Suárez-Rivero, Juan M., Pastor-Maldonado, Carmen J., Romero-González, Ana, Gómez-Fernandez, David, Povea-Cabello, Suleva, Álvarez-Córdoba, Mónica, Villalón-García, Irene, Talaverón-Rey, Marta, Suárez-Carrillo, Alejandra, Munuera-Cabeza, Manuel, Sánchez-Alcázar, José A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pharmacology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8971666/
https://www.ncbi.nlm.nih.gov/pubmed/35370630
http://dx.doi.org/10.3389/fphar.2022.862085

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8971666/
https://www.ncbi.nlm.nih.gov/pubmed/35370630
http://dx.doi.org/10.3389/fphar.2022.862085

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