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Journal Abstract Search

170 related items for PubMed ID: 16469290

  • 1. 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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  • 3. Expression and characterization of a functional canine variant of cytochrome b5 reductase.
    Roma GW, Crowley LJ, Barber MJ.
    Arch Biochem Biophys; 2006 Aug 01; 452(1):69-82. PubMed ID: 16814740
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  • 6. 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 Aug 01; 40(3):323-7. PubMed ID: 17964195
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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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  • 9. A novel L218P mutation in NADH-cytochrome b5 reductase associated with type I recessive congenital methemoglobinemia.
    Arikoglu T, Yarali N, Kara A, Bay A, Bozkaya IO, Tunc B, Percy MJ.
    Pediatr Hematol Oncol; 2009 Nov 18; 26(5):381-5. PubMed ID: 19579085
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  • 11. 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 18; 108(4):286-92. PubMed ID: 19716516
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  • 12. 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 Oct 18; 41(1):50-5. PubMed ID: 18343696
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  • 13. 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 18; 91(11):1542-5. PubMed ID: 17082011
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  • 14. Recessive congenital methaemoglobinaemia: cytochrome b(5) reductase deficiency.
    Percy MJ, Lappin TR.
    Br J Haematol; 2008 May 18; 141(3):298-308. PubMed ID: 18318771
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  • 15. NADH-cytochrome b5 reductase in a Turkish family with recessive congenital methaemoglobinaemia type I.
    Percy MJ, Aslan D.
    J Clin Pathol; 2008 Oct 18; 61(10):1122-3. PubMed ID: 18820099
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  • 16. Novel mutation (R192C) in CYB5R3 gene causing NADH-cytochrome b5 reductase deficiency in eight Indian patients associated with autosomal recessive congenital methemoglobinemia type-I.
    Kedar PS, Gupta V, Warang P, Chiddarwar A, Madkaikar M.
    Hematology; 2018 Sep 18; 23(8):567-573. PubMed ID: 29482478
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  • 17. Identification and characterization of a novel splice variant of mouse and rat cytochrome b5/cytochrome b5 reductase.
    Curry BJ, Roman SD, Wallace CA, Scott R, Miriami E, Aitken RJ.
    Genomics; 2004 Mar 18; 83(3):425-38. PubMed ID: 14962668
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  • 18. Congenital methemoglobinemia due to NADH-methemoglobin reductase deficiency in three Indian families.
    Kedar PS, Colah RB, Ghosh K, Mohanty D.
    Haematologia (Budap); 2002 Mar 18; 32(4):543-9. PubMed ID: 12803131
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  • 19. Familial Congenital Methemoglobinemia in Pomeranian Dogs Caused by a Missense Variant in the NADH-Cytochrome B5 Reductase Gene.
    Shino H, Otsuka-Yamasaki Y, Sato T, Ooi K, Inanami O, Sato R, Yamasaki M.
    J Vet Intern Med; 2018 Jan 18; 32(1):165-171. PubMed ID: 29356095
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  • 20. [Molecular analysis of the structure of the mutant NADH-cytochrome b5 reductase gene causing methemoglobinemia].
    Kobayashi Y.
    Fukuoka Igaku Zasshi; 1990 Jan 18; 81(1):41-7. PubMed ID: 2323714
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