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Gene|January 1, 1987
Isolation of a cDNA clone encoding subunit IV of human cytochrome c oxidaseM Zeviani, M Nakagawa, J Herbert, et al.Human Molecular Genetics|March 21, 2015
Cardiac deficiency of single cytochrome oxidase assembly factor scox induces p53-dependent apoptosis in a Drosophila cardiomyopathy modelLeticia Martínez-Morentin, Lidia Martínez, Sarah Piloto, et al.Human Molecular Genetics|November 15, 2011
Mitochondrial autophagy in cells with mtDNA mutations results from synergistic loss of transmembrane potential and mTORC1 inhibitionRobert W Gilkerson, Rosa L A De Vries, Paul Lebot, et al.Proceedings of the National Academy of Sciences of the United States of America|September 5, 2013
Physiological, anatomical, and behavioral changes after acoustic trauma in Drosophila melanogasterKevin W Christie, Elena Sivan-Loukianova, Wesley C Smith, et al.The Journal of Clinical Investigation|December 1, 1993
Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?C T Moraes, F Ciacci, E Bonilla, et al.EMBO Reports|December 21, 2021
Innate, translation-dependent silencing of an invasive transposon in ArabidopsisStefan Oberlin, Rajendran Rajeswaran, Marieke Trasser, et al.Revue Neurologique|January 1, 1991
Mitochondrial encephalomyopathies: biochemical approachS Dimauro, C T Moraes, S Shanske, et al.Analytical Biochemistry|May 15, 2012
Mitochondrial single nucleotide polymorphism genotyping by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry using cleavable biotinylated dideoxynucleotidesChunmei Qiu, Shiv Kumar, Jia Guo, et al.Biochemical and Biophysical Research Communications|June 11, 2002
Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutationCarla Giordano, Francesco Pallotti, Winsome F Walker, et al.Pediatric Research|November 1, 1990
Cytochrome c oxidase deficiencyS DiMauro, A Lombes, H Nakase, et al.Pageof 22