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Journal Abstract Search

220 related items for PubMed ID: 15111120

  • 1. Cytochrome b5 oxidoreductase: expression and characterization of the original familial ideopathic methemoglobinemia mutations E255- and G291D.
    Davis CA, Barber MJ.
    Arch Biochem Biophys; 2004 May 15; 425(2):123-32. PubMed ID: 15111120
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  • 2. Cytochrome b5 reductase: the roles of the recessive congenital methemoglobinemia mutants P144L, L148P, and R159*.
    Davis CA, Crowley LJ, Barber MJ.
    Arch Biochem Biophys; 2004 Nov 15; 431(2):233-44. PubMed ID: 15488472
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  • 6. Identification and characterization of the novel FAD-binding lobe G75S mutation in cytochrome b(5) reductase: an aid to determine recessive congenital methemoglobinemia status in an infant.
    Percy MJ, Crowley LJ, Roper D, Vulliamy TJ, Layton DM, Barber MJ.
    Blood Cells Mol Dis; 2006 Nov 15; 36(1):81-90. PubMed ID: 16310381
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  • 7. Mutagenesis of Glycine 179 modulates both catalytic efficiency and reduced pyridine nucleotide specificity in cytochrome b5 reductase.
    Roma GW, Crowley LJ, Davis CA, Barber MJ.
    Biochemistry; 2005 Oct 18; 44(41):13467-76. PubMed ID: 16216070
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  • 8. The structure of the S127P mutant of cytochrome b5 reductase that causes methemoglobinemia shows the AMP moiety of the flavin occupying the substrate binding site.
    Bewley MC, Davis CA, Marohnic CC, Taormina D, Barber MJ.
    Biochemistry; 2003 Nov 18; 42(45):13145-51. PubMed ID: 14609324
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  • 10. Expression of a novel P275L variant of NADH:cytochrome b5 reductase gives functional insight into the conserved motif important for pyridine nucleotide binding.
    Percy MJ, Crowley LJ, Boudreaux J, Barber MJ.
    Arch Biochem Biophys; 2006 Mar 01; 447(1):59-67. PubMed ID: 16469290
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  • 12. A novel G143D mutation in the NADH-cytochrome b5 reductase gene in an Indian patient with type I recessive hereditary methemoglobinemia.
    Kedar PS, Warang P, Nadkarni AH, Colah RB, Ghosh K.
    Blood Cells Mol Dis; 2008 Mar 01; 40(3):323-7. PubMed ID: 17964195
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  • 13. Recessive hereditary methemoglobinemia: two novel mutations in the NADH-cytochrome b5 reductase gene.
    Fermo E, Bianchi P, Vercellati C, Marcello AP, Garatti M, Marangoni O, Barcellini W, Zanella A.
    Blood Cells Mol Dis; 2008 Mar 01; 41(1):50-5. PubMed ID: 18343696
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  • 14. Engineering and characterization of a NADPH-utilizing cytochrome b5 reductase.
    Marohnic CC, Bewley MC, Barber MJ.
    Biochemistry; 2003 Sep 30; 42(38):11170-82. PubMed ID: 14503867
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  • 15. Heterologous expression of an endogenous rat cytochrome b(5)/cytochrome b(5) reductase fusion protein: identification of histidines 62 and 85 as the heme axial ligands.
    Davis CA, Dhawan IK, Johnson MK, Barber MJ.
    Arch Biochem Biophys; 2002 Apr 01; 400(1):63-75. PubMed ID: 11913972
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  • 16. Recessive congenital methaemoglobinaemia: cytochrome b(5) reductase deficiency.
    Percy MJ, Lappin TR.
    Br J Haematol; 2008 May 01; 141(3):298-308. PubMed ID: 18318771
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  • 17. A novel mutation of the cytochrome-b5 reductase gene in an Indian patient: the molecular basis of type I methemoglobinemia.
    Nussenzveig RH, Lingam HB, Gaikwad A, Zhu Q, Jing N, Prchal JT.
    Haematologica; 2006 Nov 01; 91(11):1542-5. PubMed ID: 17082011
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  • 18. Structural and mechanistic roles of three consecutive Pro residues of porcine NADH-cytochrome b(5) reductase for the binding of beta-NADH.
    Nishimura Y, Shibuya M, Muraki A, Takeuchi F, Park SY, Tsubaki M.
    J Biosci Bioeng; 2009 Oct 01; 108(4):286-92. PubMed ID: 19716516
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  • 19. Role of carboxyl residues surrounding heme of human cytochrome b5 in the electrostatic interaction with NADH-cytochrome b5 reductase.
    Kawano M, Shirabe K, Nagai T, Takeshita M.
    Biochem Biophys Res Commun; 1998 Apr 28; 245(3):666-9. PubMed ID: 9588172
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  • 20. Structure, interaction and electron transfer between cytochrome b5, its E44A and/or E56A mutants and cytochrome c.
    Sun YL, Wang YH, Yan MM, Sun BY, Xie Y, Huang ZX, Jiang SK, Wu HM.
    J Mol Biol; 1999 Jan 08; 285(1):347-59. PubMed ID: 9878411
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