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Proceedings of the National Academy of Sciences of the United States of America|November 18, 2009
Increased muscle PGC-1alpha expression protects from sarcopenia and metabolic disease during agingTina Wenz, Susana G Rossi, Richard L Rotundo, et al.The Journal of Biological Chemistry|December 6, 2006
Mutational analysis of cytochrome b at the ubiquinol oxidation site of yeast complex IIITina Wenz, Raul Covian, Petra Hellwig, et al.Mitochondrion|December 25, 2012
RETRACTED: Bezafibrate improves mitochondrial function in the CNS of a mouse model of mitochondrial encephalopathyNatalie Noe, Lloye Dillon, Veronika Lellek, et al.International Journal of Cancer|November 24, 2015
Hodgkin and Reed-Sternberg cells of classical Hodgkin lymphoma are highly dependent on oxidative phosphorylationKatrin Birkenmeier, Stefan Dröse, Ilka Wittig, et al.Human Molecular Genetics|July 27, 2010
Mitochondrial myopathy induces a starvation-like responseHenna Tyynismaa, Christopher J Carroll, Nuno Raimundo, et al.Frontiers in Genetics|August 19, 2015
Corrigendum: Long-term survival in a child with severe encephalopathy, multiple respiratory chain deficiency and GFM1 mutationsSara Brito, Kyle Thompson, Jaume Campistol, et al.Human Molecular Genetics|January 2, 2015
MTO1 mediates tissue specificity of OXPHOS defects via tRNA modification and translation optimization, which can be bypassed by dietary interventionChristin Tischner, Annette Hofer, Veronika Wulff, et al.Frontiers in Genetics|April 9, 2015
Long-term survival in a child with severe encephalopathy, multiple respiratory chain deficiency and GFM1 mutationsSara Brito, Kyle Thompson, Jaume Campistol, et al.Nature Communications|September 19, 2014
Glucose substitution prolongs maintenance of energy homeostasis and lifespan of telomere dysfunctional micePavlos Missios, Yuan Zhou, Luis Miguel Guachalla, et al.Plos One|December 16, 2014
MTO1-deficient mouse model mirrors the human phenotype showing complex I defect and cardiomyopathyLore Becker, Eva Kling, Evelyn Schiller, et al.Pageof 3