Showing results (41-50 of 351) with videos related to
Sort By:
Pageof 36
EMBO Molecular Medicine|July 22, 2015
Mitochondrial diseases caused by toxic compound accumulation: from etiopathology to therapeutic approachesIvano Di Meo, Costanza Lamperti, Valeria TirantiMethods in Molecular Biology (Clifton, N.J.)|November 24, 2020
Blue-Native Electrophoresis to Study the OXPHOS ComplexesErika Fernandez-Vizarra, Massimo ZevianiCell Cycle (Georgetown, Tex.)|December 16, 2017
Mitochondrial complex III Rieske Fe-S protein processing and assemblyErika Fernandez-Vizarra, Massimo ZevianiFrontiers in Genetics|April 28, 2015
Nuclear gene mutations as the cause of mitochondrial complex III deficiencyErika Fernández-Vizarra, Massimo ZevianiFEBS Letters|November 7, 2020
Mitochondrial disorders of the OXPHOS systemErika Fernandez-Vizarra, Massimo ZevianiBrain : a Journal of Neurology|September 11, 2004
Mitochondrial disordersMassimo Zeviani, Stefano Di DonatoAmerican Journal of Human Genetics|June 23, 2015
RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial EncephalomyopathyAurelio Reyes, Laura Melchionda, Alessia Nasca, et al.International Journal of Molecular Sciences|January 11, 2022
The Roles of Coenzyme Q in Disease: Direct and Indirect Involvement in Cellular FunctionsFrancesco Pallotti, Christian Bergamini, Costanza Lamperti, et al.Seminars in Fetal & Neonatal Medicine|May 31, 2011
Infantile mitochondrial encephalopathyGraziella Uziel, Daniele Ghezzi, Massimo ZevianiCurrent Opinion in Genetics & Development|June 6, 2003
Nuclear genes in mitochondrial disordersMassimo Zeviani, Antonella Spinazzola, Valerio CarelliPageof 36