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The Journal of Biological Chemistry|May 31, 1996
Respiration and growth defects in transmitochondrial cell lines carrying the 11778 mutation associated with Leber's hereditary optic neuropathyG Hofhaus, D R Johns, O Hurko, et al.
The Journal of Biological Chemistry|June 20, 2000
The mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode syndrome-associated human mitochondrial tRNALeu(UUR) mutation causes aminoacylation deficiency and concomitant reduced association of mRNA with ribosomesA Chomyn, J A Enriquez, V Micol, et al.
The Journal of Biological Chemistry|November 5, 1988
The site of synthesis of the iron-sulfur subunits of the flavoprotein and iron-protein fractions of human NADH dehydrogenaseA Chomyn, S D Patel, M W Cleeter, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1986
Identification of the polypeptides encoded in the unassigned reading frames 2, 4, 4L, and 5 of human mitochondrial DNAP Mariottini, A Chomyn, M Riley, et al.
American Journal of Human Genetics|June 1, 1994
Platelet-mediated transformation of mtDNA-less human cells: analysis of phenotypic variability among clones from normal individuals--and complementation behavior of the tRNALys mutation causing myoclonic epilepsy and ragged red fibersA Chomyn, S T Lai, R Shakeley, et al.
Molecular and Cellular Biology|April 1, 1991
In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondriaA Chomyn, G Meola, N Bresolin, et al.
Cell|April 1, 1983
Antibodies against synthetic peptides reveal that the unidentified reading frame A6L, overlapping the ATPase 6 gene, is expressed in human mitochondriaP Mariottini, A Chomyn, G Attardi, et al.
Science (New York, N.Y.)|October 31, 1986
URF6, last unidentified reading frame of human mtDNA, codes for an NADH dehydrogenase subunitA Chomyn, M W Cleeter, C I Ragan, et al.
American Journal of Human Genetics|October 1, 1996
The mutation rate of the human mtDNA deletion mtDNA4977R Shenkar, W Navidi, S Tavaré, et al.
The Journal of Biological Chemistry|August 2, 2001
Lack of complex I activity in human cells carrying a mutation in MtDNA-encoded ND4 subunit is corrected by the Saccharomyces cerevisiae NADH-quinone oxidoreductase (NDI1) geneY Bai, P Hájek, A Chomyn, et al.
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