Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Manuel Oropesa Avila"'
Autor:
Juan Garrido Maraver, Cordero, Mario D., Irene Domínguez Monino, Sheila Pereira Arenas, Lechuga Vieco, Ana V., David, Cotan, Mario De La Mata, Manuel Oropesa Avila, Manuel De Miguel, Juan Bautista Lorite, Eloy Rivas Infante, Manuel Alvarez Dolado, Plácido, Navas, Sandra, Jackson, Francisci, Silvia, Sanchez Alcazar, Jose A.
Publikováno v:
British journal of pharmacology. 167(6)
MELAS (mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes) is a mitochondrial disease most usually caused by point mutations in tRNA genes encoded by mitochondrial DNA (mtDNA). Approximately 80% of cases of MELAS syndrome are a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::3be879575d9110839828e5943dec690f
https://pubmed.ncbi.nlm.nih.gov/22747838
https://pubmed.ncbi.nlm.nih.gov/22747838
Autor:
José A. Sánchez Alcázar, Manuel Oropesa Ávila, Yuniesky Andrade Talavera, Juan Garrido Maraver, Isabel de Lavera, Mario de la Mata, David Cotán, Marina Villanueva Paz, Ana Delgado Pavón, Elisabet Alcocer Gómez, Antonio Rodríguez Moreno
Publikováno v:
Redox Biology, Vol 5, Iss , Pp 416- (2015)
Apoptosis is characterized by degradation of cell components but plasma membrane remains intact. Apoptotic microtubule network (AMN) is organized during apoptosis forming a cortical structure beneath plasma membrane that maintains plasma membrane int
Externí odkaz:
https://doaj.org/article/69ddffef266b4a6abdcb6d72b76913a8