BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

191 related articles for article (PubMed ID: 26160915)

  • 1. COA6 is a mitochondrial complex IV assembly factor critical for biogenesis of mtDNA-encoded COX2.
    Stroud DA; Maher MJ; Lindau C; Vögtle FN; Frazier AE; Surgenor E; Mountford H; Singh AP; Bonas M; Oeljeklaus S; Warscheid B; Meisinger C; Thorburn DR; Ryan MT
    Hum Mol Genet; 2015 Oct; 24(19):5404-15. PubMed ID: 26160915
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cooperation between COA6 and SCO2 in COX2 maturation during cytochrome c oxidase assembly links two mitochondrial cardiomyopathies.
    Pacheu-Grau D; Bareth B; Dudek J; Juris L; Vögtle FN; Wissel M; Leary SC; Dennerlein S; Rehling P; Deckers M
    Cell Metab; 2015 Jun; 21(6):823-33. PubMed ID: 25959673
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mitochondrial disease genes COA6, COX6B and SCO2 have overlapping roles in COX2 biogenesis.
    Ghosh A; Pratt AT; Soma S; Theriault SG; Griffin AT; Trivedi PP; Gohil VM
    Hum Mol Genet; 2016 Feb; 25(4):660-71. PubMed ID: 26669719
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Human mitochondrial cytochrome
    Bourens M; Barrientos A
    J Biol Chem; 2017 May; 292(19):7774-7783. PubMed ID: 28330871
    [TBL] [Abstract][Full Text] [Related]  

  • 5. COA6 Facilitates Cytochrome c Oxidase Biogenesis as Thiol-reductase for Copper Metallochaperones in Mitochondria.
    Pacheu-Grau D; Wasilewski M; Oeljeklaus S; Gibhardt CS; Aich A; Chudenkova M; Dennerlein S; Deckers M; Bogeski I; Warscheid B; Chacinska A; Rehling P
    J Mol Biol; 2020 Mar; 432(7):2067-2079. PubMed ID: 32061935
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations in COA6 cause cytochrome c oxidase deficiency and neonatal hypertrophic cardiomyopathy.
    Baertling F; A M van den Brand M; Hertecant JL; Al-Shamsi A; P van den Heuvel L; Distelmaier F; Mayatepek E; Smeitink JA; Nijtmans LG; Rodenburg RJ
    Hum Mutat; 2015 Jan; 36(1):34-8. PubMed ID: 25339201
    [TBL] [Abstract][Full Text] [Related]  

  • 7. COX16 promotes COX2 metallation and assembly during respiratory complex IV biogenesis.
    Aich A; Wang C; Chowdhury A; Ronsör C; Pacheu-Grau D; Richter-Dennerlein R; Dennerlein S; Rehling P
    Elife; 2018 Jan; 7():. PubMed ID: 29381136
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The Role of COA6 in the Mitochondrial Copper Delivery Pathway to Cytochrome
    Swaminathan AB; Gohil VM
    Biomolecules; 2022 Jan; 12(1):. PubMed ID: 35053273
    [TBL] [Abstract][Full Text] [Related]  

  • 9. COA6 Is Structurally Tuned to Function as a Thiol-Disulfide Oxidoreductase in Copper Delivery to Mitochondrial Cytochrome c Oxidase.
    Soma S; Morgada MN; Naik MT; Boulet A; Roesler AA; Dziuba N; Ghosh A; Yu Q; Lindahl PA; Ames JB; Leary SC; Vila AJ; Gohil VM
    Cell Rep; 2019 Dec; 29(12):4114-4126.e5. PubMed ID: 31851937
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Loss of function of Sco1 and its interaction with cytochrome c oxidase.
    Stiburek L; Vesela K; Hansikova H; Hulkova H; Zeman J
    Am J Physiol Cell Physiol; 2009 May; 296(5):C1218-26. PubMed ID: 19295170
    [TBL] [Abstract][Full Text] [Related]  

  • 11. What Role Does COA6 Play in Cytochrome
    Maghool S; Ryan MT; Maher MJ
    Int J Mol Sci; 2020 Sep; 21(19):. PubMed ID: 32977416
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Structural and functional characterization of the mitochondrial complex IV assembly factor Coa6.
    Maghool S; Cooray NDG; Stroud DA; Aragão D; Ryan MT; Maher MJ
    Life Sci Alliance; 2019 Oct; 2(5):. PubMed ID: 31515291
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Copper supplementation restores cytochrome c oxidase assembly defect in a mitochondrial disease model of COA6 deficiency.
    Ghosh A; Trivedi PP; Timbalia SA; Griffin AT; Rahn JJ; Chan SS; Gohil VM
    Hum Mol Genet; 2014 Jul; 23(13):3596-606. PubMed ID: 24549041
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Human COX20 cooperates with SCO1 and SCO2 to mature COX2 and promote the assembly of cytochrome c oxidase.
    Bourens M; Boulet A; Leary SC; Barrientos A
    Hum Mol Genet; 2014 Jun; 23(11):2901-13. PubMed ID: 24403053
    [TBL] [Abstract][Full Text] [Related]  

  • 15. COX16 is required for assembly of cytochrome c oxidase in human cells and is involved in copper delivery to COX2.
    Cerqua C; Morbidoni V; Desbats MA; Doimo M; Frasson C; Sacconi S; Baldoin MC; Sartori G; Basso G; Salviati L; Trevisson E
    Biochim Biophys Acta Bioenerg; 2018 Apr; 1859(4):244-252. PubMed ID: 29355485
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The mitochondrial TMEM177 associates with COX20 during COX2 biogenesis.
    Lorenzi I; Oeljeklaus S; Aich A; Ronsör C; Callegari S; Dudek J; Warscheid B; Dennerlein S; Rehling P
    Biochim Biophys Acta Mol Cell Res; 2018 Feb; 1865(2):323-333. PubMed ID: 29154948
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The human cytochrome c oxidase assembly factors SCO1 and SCO2 have regulatory roles in the maintenance of cellular copper homeostasis.
    Leary SC; Cobine PA; Kaufman BA; Guercin GH; Mattman A; Palaty J; Lockitch G; Winge DR; Rustin P; Horvath R; Shoubridge EA
    Cell Metab; 2007 Jan; 5(1):9-20. PubMed ID: 17189203
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The scoop on Sco.
    Brière JJ; Tzagoloff A
    Mol Cell; 2007 Jan; 25(2):176-8. PubMed ID: 17244525
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A mutation in the FAM36A gene, the human ortholog of COX20, impairs cytochrome c oxidase assembly and is associated with ataxia and muscle hypotonia.
    Szklarczyk R; Wanschers BF; Nijtmans LG; Rodenburg RJ; Zschocke J; Dikow N; van den Brand MA; Hendriks-Franssen MG; Gilissen C; Veltman JA; Nooteboom M; Koopman WJ; Willems PH; Smeitink JA; Huynen MA; van den Heuvel LP
    Hum Mol Genet; 2013 Feb; 22(4):656-67. PubMed ID: 23125284
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Human SCO2 is required for the synthesis of CO II and as a thiol-disulphide oxidoreductase for SCO1.
    Leary SC; Sasarman F; Nishimura T; Shoubridge EA
    Hum Mol Genet; 2009 Jun; 18(12):2230-40. PubMed ID: 19336478
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.