Regulation of NADH/CoQ oxidoreductase: do phosphorylation events affect activity?
Maj, Mary C, Raha, Sandeep, Myint, Tomoko, Robinson, Brian H
Published in The Protein Journal (01.01.2004)
Published in The Protein Journal (01.01.2004)
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Clinical variability in maternally inherited leber hereditary optic neuropathy with the G14459A mutation
Tarnopolsky, Mark A., Baker, Steven K., Myint, Tomoko, Maxner, C.E., Robitaille, J., Robinson, Brian H.
Published in American journal of medical genetics. Part A (01.02.2004)
Published in American journal of medical genetics. Part A (01.02.2004)
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Journal Article
Superoxides from mitochondrial complex III: the role of manganese superoxide dismutase
Raha, Sandeep, McEachern, Gillian E, Myint, A.Tomoko, Robinson, Brian H
Published in Free radical biology & medicine (15.07.2000)
Published in Free radical biology & medicine (15.07.2000)
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Repopulation of Á0 cells with mitochondria from a patient with a mitochondrial DNA point mutation in tRNAGly results in respiratory chain dysfunction
Raha, Sandeep, Merante, Frank, Shoubridge, Eric, A. Tomoko Myint, Tein, Ingrid, Benson, Lee, Johns, Tim, Robinson, Brian H
Published in Human mutation (01.01.1999)
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Published in Human mutation (01.01.1999)
Journal Article
Repopulation of ρ0 cells with mitochondria from a patient with a mitochondrial DNA point mutation in tRNAGly results in respiratory chain dysfunction
Raha, Sandeep, Merante, Frank, Shoubridge, Eric, Myint, A. Tomoko, Tein, Ingrid, Benson, Lee, Johns, Tim, Robinson, Brian H.
Published in Human mutation (1999)
Published in Human mutation (1999)
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Journal Article
Repopulation of ?0 cells with mitochondria from a patient with a mitochondrial DNA point mutation in tRNAGly results in respiratory chain dysfunction
Raha, Sandeep, Merante, Frank, Shoubridge, Eric, Myint, A. Tomoko, Tein, Ingrid, Benson, Lee, Johns, Tim, Robinson, Brian H.
Published in Human mutation (1999)
Published in Human mutation (1999)
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Journal Article
The expanding clinical phenotype of the tRNA(Leu(UUR)) A-->G mutation at np 3243 of mitochondrial DNA: diabetic embryopathy associated with mitochondrial cytopathy
Feigenbaum, A, Chitayat, D, Robinson, B, MacGregor, D, Myint, T, Arbus, G, Nowaczyk, M J
Published in American journal of medical genetics (24.04.1996)
Published in American journal of medical genetics (24.04.1996)
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