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Journal Abstract Search

193 related items for PubMed ID: 9878253

  • 1. Identification and characterization of human cDNAs specific to BCS1, PET112, SCO1, COX15, and COX11, five genes involved in the formation and function of the mitochondrial respiratory chain.
    Petruzzella V, Tiranti V, Fernandez P, Ianna P, Carrozzo R, Zeviani M.
    Genomics; 1998 Dec 15; 54(3):494-504. PubMed ID: 9878253
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  • 2. Specific copper transfer from the Cox17 metallochaperone to both Sco1 and Cox11 in the assembly of yeast cytochrome C oxidase.
    Horng YC, Cobine PA, Maxfield AB, Carr HS, Winge DR.
    J Biol Chem; 2004 Aug 20; 279(34):35334-40. PubMed ID: 15199057
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  • 3. Novel COX11 Mutations Associated with Mitochondrial Disorder: Functional Characterization in Patient Fibroblasts and Saccharomyces cerevisiae.
    Caron-Godon CA, Della Vecchia S, Romano A, Doccini S, Dal Canto F, Pasquariello R, Rubegni A, Battini R, Santorelli FM, Glerum DM, Nesti C.
    Int J Mol Sci; 2023 Nov 23; 24(23):. PubMed ID: 38068960
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  • 4. HCC1, the Arabidopsis homologue of the yeast mitochondrial copper chaperone SCO1, is essential for embryonic development.
    Steinebrunner I, Landschreiber M, Krause-Buchholz U, Teichmann J, Rödel G.
    J Exp Bot; 2011 Jan 23; 62(1):319-30. PubMed ID: 21041373
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  • 5. Analysis of Oligomerization Properties of Heme a Synthase Provides Insights into Its Function in Eukaryotes.
    Swenson S, Cannon A, Harris NJ, Taylor NG, Fox JL, Khalimonchuk O.
    J Biol Chem; 2016 May 06; 291(19):10411-25. PubMed ID: 26940873
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  • 6. hCOX18 and hCOX19: two human genes involved in cytochrome c oxidase assembly.
    Sacconi S, Trevisson E, Pistollato F, Baldoin MC, Rezzonico R, Bourget I, Desnuelle C, Tenconi R, Basso G, DiMauro S, Salviati L.
    Biochem Biophys Res Commun; 2005 Nov 25; 337(3):832-9. PubMed ID: 16212937
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  • 11. Characterization of human SCO1 and COX17 genes in mitochondrial cytochrome-c-oxidase deficiency.
    Horvath R, Lochmüller H, Stucka R, Yao J, Shoubridge EA, Kim SH, Gerbitz KD, Jaksch M.
    Biochem Biophys Res Commun; 2000 Sep 24; 276(2):530-3. PubMed ID: 11027508
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  • 16. Chemicals or mutations that target mitochondrial translation can rescue the respiratory deficiency of yeast bcs1 mutants.
    Panozzo C, Laleve A, Tribouillard-Tanvier D, Ostojić J, Sellem CH, Friocourt G, Bourand-Plantefol A, Burg A, Delahodde A, Blondel M, Dujardin G.
    Biochim Biophys Acta Mol Cell Res; 2017 Dec 24; 1864(12):2297-2307. PubMed ID: 28888990
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  • 17. Cox17 is functional when tethered to the mitochondrial inner membrane.
    Maxfield AB, Heaton DN, Winge DR.
    J Biol Chem; 2004 Feb 13; 279(7):5072-80. PubMed ID: 14615477
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  • 18. Human SCO1 and SCO2 have independent, cooperative functions in copper delivery to cytochrome c oxidase.
    Leary SC, Kaufman BA, Pellecchia G, Guercin GH, Mattman A, Jaksch M, Shoubridge EA.
    Hum Mol Genet; 2004 Sep 01; 13(17):1839-48. PubMed ID: 15229189
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  • 19. BCS1, a novel gene required for the expression of functional Rieske iron-sulfur protein in Saccharomyces cerevisiae.
    Nobrega FG, Nobrega MP, Tzagoloff A.
    EMBO J; 1992 Nov 01; 11(11):3821-9. PubMed ID: 1327750
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  • 20. SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome.
    Zhu Z, Yao J, Johns T, Fu K, De Bie I, Macmillan C, Cuthbert AP, Newbold RF, Wang J, Chevrette M, Brown GK, Brown RM, Shoubridge EA.
    Nat Genet; 1998 Dec 01; 20(4):337-43. PubMed ID: 9843204
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