UPR(mt) activation improves pathological alterations in cellular models of mitochondrial diseases

BACKGROUND: Mitochondrial diseases represent one of the most common groups of genetic diseases. With a prevalence greater than 1 in 5000 adults, such diseases still lack effective treatment. Current therapies are purely palliative and, in most cases, insufficient. Novel approaches to compensate and,...

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Detalles Bibliográficos
Autores principales: Suárez-Rivero, Juan M., Pastor-Maldonado, Carmen J., Povea-Cabello, Suleva, Álvarez-Córdoba, Mónica, Villalón-García, Irene, Talaverón-Rey, Marta, Suárez-Carrillo, Alejandra, Munuera-Cabeza, Manuel, Reche-López, Diana, Cilleros-Holgado, Paula, Piñero-Perez, Rocío, Sánchez-Alcázar, José A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9115953/
https://www.ncbi.nlm.nih.gov/pubmed/35581596
http://dx.doi.org/10.1186/s13023-022-02331-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9115953/
https://www.ncbi.nlm.nih.gov/pubmed/35581596
http://dx.doi.org/10.1186/s13023-022-02331-8

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