Publications

Found 61 results
Filters: Keyword is Electron Transport Complex IV  [Clear All Filters]
1992
Fabrizi GM, Sadlock J, Hirano M, Mita S, Koga Y, Rizzuto R, Zeviani M & Schon EA (1992) Differential expression of genes specifying two isoforms of subunit VIa of human cytochrome c oxidase. Gene 119, 307-12
1989
DiMauro S, Zeviani M, Moraes CT, Nakase H, Rizzuto R, Lombès A, Shanske S & Schon EA (1989) Mitochondrial encephalomyopathies. Prog Clin Biol Res 306, 117-28
1988
Schon EA, Bonilla E, Lombès A, Moraes CT, Nakase H, Rizzuto R, Zeviani M & DiMauro S (1988) Clinical and biochemical studies on cytochrome oxidase deficiencies. Ann N Y Acad Sci 550, 348-59
DiMauro S, Zeviani M, Rizzuto R, Lombès A, Nakase H, Bonilla E, Miranda A & Schon E (1988) Molecular defects in cytochrome oxidase in mitochondrial diseases. J Bioenerg Biomembr 20, 353-64
Zeviani M, Sakoda S, Sherbany AA, Nakase H, Rizzuto R, Samitt CE, DiMauro S & Schon EA (1988) Sequence of cDNAs encoding subunit Vb of human and bovine cytochrome c oxidase. Gene 65, 1-11
Rizzuto R, Nakase H, Zeviani M, DiMauro S & Schon EA (1988) Subunit Va of human and bovine cytochrome c oxidase is highly conserved. Gene 69, 245-56
1987
Zeviani M, Nakagawa M, Herbert J, Lomax MI, Grossman LI, Sherbany AA, Miranda AF, DiMauro S & Schon EA (1987) Isolation of a cDNA clone encoding subunit IV of human cytochrome c oxidase. Gene 55, 205-17
1986
DiMauro S, Zeviani M, Servidei S, Bonilla E, Miranda AF, Prelle A & Schon EA (1986) Cytochrome oxidase deficiency: clinical and biochemical heterogeneity. Ann N Y Acad Sci 488, 19-32
1985
DiMauro S, Zeviani M, Bonilla E, Bresolin N, Nakagawa M, Miranda AF & Moggio M (1985) Cytochrome c oxidase deficiency. Biochem Soc Trans 13, 651-3
Bresolin N, Zeviani M, Bonilla E, Miller RH, Leech RW, Shanske S, Nakagawa M & DiMauro S (1985) Fatal infantile cytochrome c oxidase deficiency: decrease of immunologically detectable enzyme in muscle. Neurology 35, 802-12
Zeviani M, Nonaka I, Bonilla E, Okino E, Moggio M, Jones S & DiMauro S (1985) Fatal infantile mitochondrial myopathy and renal dysfunction caused by cytochrome c oxidase deficiency: immunological studies in a new patient. Ann Neurol 17, 414-7

Pages