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Muscle & Nerve|March 1, 1994
Skeletal muscle mitochondrial myopathy as a cause of exercise intolerance in a horseS J Valberg, G P Carlson, G H Cardinet, et al.Proceedings of the National Academy of Sciences of the United States of America|September 1, 1983
Identification of the polypeptides encoded in the ATPase 6 gene and in the unassigned reading frames 1 and 3 of human mtDNAA Chomyn, P Mariottini, N Gonzalez-Cadavid, et al.Nature|April 18, 1985
Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenaseA Chomyn, P Mariottini, M W Cleeter, et al.Biochimica Et Biophysica Acta|March 8, 1995
Multiple deficiencies of mitochondrial DNA- and nuclear-encoded subunits of respiratory NADH dehydrogenase detected with peptide- and subunit-specific antibodies in mitochondrial myopathiesH A Bentlage, A J Janssen, A Chomyn, et al.Proceedings of the National Academy of Sciences of the United States of America|May 15, 1992
MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcriptsA Chomyn, A Martinuzzi, M Yoneda, et al.Journal of Neurology|November 1, 1990
A case of mitochondrial myopathy, lactic acidosis and complex I deficiencyL Bet, N Bresolin, M Moggio, et al.Pageof 3