Cargando…
Impact of the Mitochondrial Genetic Background in Complex III Deficiency
BACKGROUND: In recent years clinical evidence has emphasized the importance of the mtDNA genetic background that hosts a primary pathogenic mutation in the clinical expression of mitochondrial disorders, but little experimental confirmation has been provided. We have analyzed the pathogenic role of...
Autores principales: | Gil Borlado, Mari Carmen, Moreno Lastres, David, Gonzalez Hoyuela, Maritza, Moran, Maria, Blazquez, Alberto, Pello, Rosa, Marin Buera, Lorena, Gabaldon, Toni, Garcia Peñas, Juan Jose, Martín, Miguel A., Arenas, Joaquin, Ugalde, Cristina |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2941448/ https://www.ncbi.nlm.nih.gov/pubmed/20862300 http://dx.doi.org/10.1371/journal.pone.0012801 |
Ejemplares similares
-
Altered Expression Ratio of Actin-Binding Gelsolin Isoforms Is a Novel Hallmark of Mitochondrial OXPHOS Dysfunction
por: García-Bartolomé, Alberto, et al.
Publicado: (2020) -
Novel NDUFA13 Mutations Associated with OXPHOS Deficiency and Leigh Syndrome: A Second Family Report
por: González-Quintana, Adrián, et al.
Publicado: (2020) -
Regulation of Mitochondrial Function by the Actin Cytoskeleton
por: Illescas, María, et al.
Publicado: (2021) -
Aging, NRF2, and TAU: A Perfect Match for Neurodegeneration?
por: Brackhan, Mirjam, et al.
Publicado: (2023) -
Five-year outcomes of laparoscopic sleeve gastrectomy as a primary procedure for morbid obesity: A prospective study
por: Hoyuela, Carlos
Publicado: (2017)