BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

222 related articles for article (PubMed ID: 19625251)

  • 1. Surf1, associated with Leigh syndrome in humans, is a heme-binding protein in bacterial oxidase biogenesis.
    Bundschuh FA; Hannappel A; Anderka O; Ludwig B
    J Biol Chem; 2009 Sep; 284(38):25735-41. PubMed ID: 19625251
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Characterization of heme-binding properties of Paracoccus denitrificans Surf1 proteins.
    Hannappel A; Bundschuh FA; Ludwig B
    FEBS J; 2011 May; 278(10):1769-78. PubMed ID: 21418525
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Two variants of the assembly factor Surf1 target specific terminal oxidases in Paracoccus denitrificans.
    Bundschuh FA; Hoffmeier K; Ludwig B
    Biochim Biophys Acta; 2008 Oct; 1777(10):1336-43. PubMed ID: 18582433
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Role of Surf1 in heme recruitment for bacterial COX biogenesis.
    Hannappel A; Bundschuh FA; Ludwig B
    Biochim Biophys Acta; 2012 Jun; 1817(6):928-37. PubMed ID: 21945856
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Adaptation of respiratory chain biogenesis to cytochrome c oxidase deficiency caused by SURF1 gene mutations.
    Kovářová N; Cížková Vrbacká A; Pecina P; Stránecký V; Pronicka E; Kmoch S; Houštěk J
    Biochim Biophys Acta; 2012 Jul; 1822(7):1114-24. PubMed ID: 22465034
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Tissue- and species-specific differences in cytochrome c oxidase assembly induced by SURF1 defects.
    Kovářová N; Pecina P; Nůsková H; Vrbacký M; Zeviani M; Mráček T; Viscomi C; Houštěk J
    Biochim Biophys Acta; 2016 Apr; 1862(4):705-715. PubMed ID: 26804654
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel p.P298L SURF1 mutation in thiamine deficient Leigh syndrome patients compromises cytochrome c oxidase activity.
    Mani S; Chandak GR; Singh KK; Singh R; Rao SN
    Mitochondrion; 2020 Jul; 53():91-98. PubMed ID: 32380162
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cytochrome c oxidase subassemblies in fibroblast cultures from patients carrying mutations in COX10, SCO1, or SURF1.
    Williams SL; Valnot I; Rustin P; Taanman JW
    J Biol Chem; 2004 Feb; 279(9):7462-9. PubMed ID: 14607829
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Deciphering protein-protein interactions during the biogenesis of cytochrome c oxidase from Paracoccus denitrificans.
    Gurumoorthy P; Ludwig B
    FEBS J; 2015 Feb; 282(3):537-49. PubMed ID: 25420759
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 291(19):10411-25. PubMed ID: 26940873
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sequence conservation from human to prokaryotes of Surf1, a protein involved in cytochrome c oxidase assembly, deficient in Leigh syndrome.
    Poyau A; Buchet K; Godinot C
    FEBS Lett; 1999 Dec; 462(3):416-20. PubMed ID: 10622737
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Missense mutations in SURF1 associated with deficient cytochrome c oxidase assembly in Leigh syndrome patients.
    Poyau A; Buchet K; Bouzidi MF; Zabot MT; Echenne B; Yao J; Shoubridge EA; Godinot C
    Hum Genet; 2000 Feb; 106(2):194-205. PubMed ID: 10746561
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cytochrome C oxydase deficiency: SURF1 gene investigation in patients with Leigh syndrome.
    Maalej M; Kammoun T; Alila-Fersi O; Kharrat M; Ammar M; Felhi R; Mkaouar-Rebai E; Keskes L; Hachicha M; Fakhfakh F
    Biochem Biophys Res Commun; 2018 Mar; 497(4):1043-1048. PubMed ID: 29481804
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [A new missense mutation of 574C>T in the SURF1 gene--biochemical and molecular genetic study in seven children with Leigh syndrome].
    Capková M; Hansíková H; Godinot C; Houst'ková H; Houstĕk J; Zeman J
    Cas Lek Cesk; 2002 Oct; 141(20):636-41. PubMed ID: 12515039
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Leigh syndrome in Drosophila melanogaster: morphological and biochemical characterization of Surf1 post-transcriptional silencing.
    Da-Rè C; von Stockum S; Biscontin A; Millino C; Cisotto P; Zordan MA; Zeviani M; Bernardi P; De Pittà C; Costa R
    J Biol Chem; 2014 Oct; 289(42):29235-46. PubMed ID: 25164807
    [TBL] [Abstract][Full Text] [Related]  

  • 16. SURF1 knockout cloned pigs: Early onset of a severe lethal phenotype.
    Quadalti C; Brunetti D; Lagutina I; Duchi R; Perota A; Lazzari G; Cerutti R; Di Meo I; Johnson M; Bottani E; Crociara P; Corona C; Grifoni S; Tiranti V; Fernandez-Vizarra E; Robinson AJ; Viscomi C; Casalone C; Zeviani M; Galli C
    Biochim Biophys Acta Mol Basis Dis; 2018 Jun; 1864(6 Pt A):2131-2142. PubMed ID: 29601977
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Redox dependent changes at the heme propionates in cytochrome c oxidase from Paracoccus denitrificans: direct evidence from FTIR difference spectroscopy in combination with heme propionate 13C labeling.
    Behr J; Hellwig P; Mäntele W; Michel H
    Biochemistry; 1998 May; 37(20):7400-6. PubMed ID: 9585554
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Functional alteration of cytochrome c oxidase by SURF1 mutations in Leigh syndrome.
    Pecina P; Capková M; Chowdhury SK; Drahota Z; Dubot A; Vojtísková A; Hansíková H; Houst'ková H; Zeman J; Godinot C; Houstek J
    Biochim Biophys Acta; 2003 Sep; 1639(1):53-63. PubMed ID: 12943968
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Expression and functional analysis of SURF1 in Leigh syndrome patients with cytochrome c oxidase deficiency.
    Yao J; Shoubridge EA
    Hum Mol Genet; 1999 Dec; 8(13):2541-9. PubMed ID: 10556303
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 20(4):337-43. PubMed ID: 9843204
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.