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Journal Abstract Search

175 related items for PubMed ID: 15596615

  • 21. A microdeletion in cytochrome c oxidase (COX) subunit III associated with COX deficiency and recurrent myoglobinuria.
    Keightley JA, Hoffbuhr KC, Burton MD, Salas VM, Johnston WS, Penn AM, Buist NR, Kennaway NG.
    Nat Genet; 1996 Apr; 12(4):410-6. PubMed ID: 8630495
    [Abstract] [Full Text] [Related]

  • 22. 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
    [Abstract] [Full Text] [Related]

  • 23. High-resolution melting analysis of 15 genes in 60 patients with cytochrome-c oxidase deficiency.
    Vondrackova A, Vesela K, Hansikova H, Docekalova DZ, Rozsypalova E, Zeman J, Tesarova M.
    J Hum Genet; 2012 Jul 25; 57(7):442-8. PubMed ID: 22592081
    [Abstract] [Full Text] [Related]

  • 24. Mutations in mitochondrial-encoded cytochrome c oxidase subunits I, II, and III genes detected in Alzheimer's disease using single-strand conformation polymorphism.
    Hamblet NS, Ragland B, Ali M, Conyers B, Castora FJ.
    Electrophoresis; 2006 Feb 25; 27(2):398-408. PubMed ID: 16358358
    [Abstract] [Full Text] [Related]

  • 25. 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
    [Abstract] [Full Text] [Related]

  • 26. Leigh syndrome with cytochrome-c oxidase deficiency and a single T insertion nt 5537 in the mitochondrial tRNATrp gene.
    Tulinius M, Moslemi AR, Darin N, Westerberg B, Wiklund LM, Holme E, Oldfors A.
    Neuropediatrics; 2003 Apr 01; 34(2):87-91. PubMed ID: 12776230
    [Abstract] [Full Text] [Related]

  • 27. Human cytochrome oxidase deficiency.
    Robinson BH.
    Pediatr Res; 2000 Nov 01; 48(5):581-5. PubMed ID: 11044474
    [Abstract] [Full Text] [Related]

  • 28. Sequence and chromosomal localization of two PET genes required for cytochrome c oxidase assembly in Saccharomyces cerevisiae.
    McEwen JE, Hong KH, Park S, Preciado GT.
    Curr Genet; 1993 Jan 01; 23(1):9-14. PubMed ID: 8381337
    [Abstract] [Full Text] [Related]

  • 29. A novel mutation in the mitochondrial tRNA Asn gene associated with a lethal disease.
    Coulbault L, Herlicoviez D, Chapon F, Read MH, Penniello MJ, Reynier P, Fayet G, Lombès A, Jauzac P, Allouche S.
    Biochem Biophys Res Commun; 2005 Apr 15; 329(3):1152-4. PubMed ID: 15752774
    [Abstract] [Full Text] [Related]

  • 30. Cytochrome c oxidase deficiency in a child with isolated myopathy.
    Karadag A, Avci Z, Catal F, Odemis E.
    Fetal Pediatr Pathol; 2005 Apr 15; 24(3):149-53. PubMed ID: 16338876
    [Abstract] [Full Text] [Related]

  • 31. characterization of the cytochrome c oxidase assembly factor Cox19 of Saccharomyces cerevisiae.
    Rigby K, Zhang L, Cobine PA, George GN, Winge DR.
    J Biol Chem; 2007 Apr 06; 282(14):10233-42. PubMed ID: 17237235
    [Abstract] [Full Text] [Related]

  • 32. Sequence analysis of the structural nuclear encoded subunits and assembly genes of cytochrome c oxidase in a cohort of 10 isolated complex IV-deficient patients revealed five mutations.
    Coenen MJ, Smeitink JA, Pots JM, van Kaauwen E, Trijbels FJ, Hol FA, van den Heuvel LP.
    J Child Neurol; 2006 Jun 06; 21(6):508-11. PubMed ID: 16948936
    [Abstract] [Full Text] [Related]

  • 33. The P(174)L mutation in the human hSCO1 gene affects the assembly of cytochrome c oxidase.
    Paret C, Lode A, Krause-Buchholz U, Rödel G.
    Biochem Biophys Res Commun; 2000 Dec 20; 279(2):341-7. PubMed ID: 11118289
    [Abstract] [Full Text] [Related]

  • 34. Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathy.
    Meulemans A, De Paepe B, De Bleecker J, Smet J, Lissens W, Van Coster R, De Meirleir L, Seneca S.
    Arch Neurol; 2007 Sep 20; 64(9):1339-43. PubMed ID: 17846276
    [Abstract] [Full Text] [Related]

  • 35.
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  • 36. Association of mutations in SCO2, a cytochrome c oxidase assembly gene, with early fetal lethality.
    Tay SK, Shanske S, Kaplan P, DiMauro S.
    Arch Neurol; 2004 Jun 20; 61(6):950-2. PubMed ID: 15210538
    [Abstract] [Full Text] [Related]

  • 37. The Bax lnhibitor-1 needs a functional electron transport chain for cell death suppression.
    Oshima R, Yoshinaga K, Ihara-Ohori Y, Fukuda R, Ohta A, Uchimiya H, Kawai-Yamada M.
    FEBS Lett; 2007 Oct 02; 581(24):4627-32. PubMed ID: 17825821
    [Abstract] [Full Text] [Related]

  • 38. Is nuclear respiratory factor 2 a master transcriptional coordinator for all ten nuclear-encoded cytochrome c oxidase subunits in neurons?
    Ongwijitwat S, Wong-Riley MT.
    Gene; 2005 Oct 24; 360(1):65-77. PubMed ID: 16126350
    [Abstract] [Full Text] [Related]

  • 39. High prevalence of SURF1 c.845_846delCT mutation in Polish Leigh patients.
    Piekutowska-Abramczuk D, Popowska E, Pronicki M, Karczmarewicz E, Tylek-Lemanska D, Sykut-Cegielska J, Szymanska-Dembinska T, Bielecka L, Krajewska-Walasek M, Pronicka E.
    Eur J Paediatr Neurol; 2009 Mar 24; 13(2):146-53. PubMed ID: 18583168
    [Abstract] [Full Text] [Related]

  • 40. The mitochondrial copper chaperone COX19 influences copper and iron homeostasis in arabidopsis.
    Garcia L, Mansilla N, Ocampos N, Pagani MA, Welchen E, Gonzalez DH.
    Plant Mol Biol; 2019 Apr 24; 99(6):621-638. PubMed ID: 30778722
    [Abstract] [Full Text] [Related]

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