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Gene|May 15, 1988
Sequence of cDNAs encoding subunit Vb of human and bovine cytochrome c oxidaseM Zeviani, S Sakoda, A A Sherbany, et al.Neurology|April 1, 1991
Biochemical and molecular analysis of cytochrome c oxidase deficiency in Leigh's syndromeA Lombes, H Nakase, H J Tritschler, et al.Proceedings of the National Academy of Sciences of the United States of America|August 9, 2008
The kinase domain of mitochondrial PINK1 faces the cytoplasmChun Zhou, Yong Huang, Yufang Shao, et al.Cell Metabolism|July 5, 2011
In vivo correction of COX deficiency by activation of the AMPK/PGC-1α axisCarlo Viscomi, Emanuela Bottani, Gabriele Civiletto, et al.Muscle & Nerve. Supplement|January 1, 1995
Phenotype-genotype correlations in skeletal muscle of patients with mtDNA deletionsC T Moraes, M Sciacco, E Ricci, et al.The Journal of Biological Chemistry|September 15, 1989
Structure of the gene encoding the muscle-specific subunit of human phosphoglycerate mutaseS Tsujino, S Sakoda, R Mizuno, et al.Cell Death & Disease|March 2, 2018
A key role for MAM in mediating mitochondrial dysfunction in Alzheimer diseaseEstela Area-Gomez, Ad de Groof, Eduardo Bonilla, et al.Neuromuscular Disorders : NMD|January 1, 1993
Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNAC T Moraes, F Ciacci, G Silvestri, et al.Annals of Neurology|August 1, 1997
Association of myopathy with large-scale mitochondrial DNA duplications and deletions: which is pathogenic?G Manfredi, T Vu, E Bonilla, et al.The Journal of Biological Chemistry|March 27, 1999
Oligomycin induces a decrease in the cellular content of a pathogenic mutation in the human mitochondrial ATPase 6 geneG Manfredi, N Gupta, M E Vazquez-Memije, et al.Pageof 22