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160 related items for PubMed ID: 10801779

  • 1. Deletion mutation in Drosophila ma-l homologous, putative molybdopterin cofactor sulfurase gene is associated with bovine xanthinuria type II.
    Watanabe T, Ihara N, Itoh T, Fujita T, Sugimoto Y.
    J Biol Chem; 2000 Jul 21; 275(29):21789-92. PubMed ID: 10801779
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  • 2. Mutation of human molybdenum cofactor sulfurase gene is responsible for classical xanthinuria type II.
    Ichida K, Matsumura T, Sakuma R, Hosoya T, Nishino T.
    Biochem Biophys Res Commun; 2001 Apr 20; 282(5):1194-200. PubMed ID: 11302742
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  • 3. Identification and characterization of the first mutation (Arg776Cys) in the C-terminal domain of the Human Molybdenum Cofactor Sulfurase (HMCS) associated with type II classical xanthinuria.
    Peretz H, Naamati MS, Levartovsky D, Lagziel A, Shani E, Horn I, Shalev H, Landau D.
    Mol Genet Metab; 2007 May 20; 91(1):23-9. PubMed ID: 17368066
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  • 5. [Hereditary xanthinuria and molybdenum cofactor deficiency].
    Ichida K.
    Nihon Rinsho; 2003 Jan 20; 61 Suppl 1():377-82. PubMed ID: 12629751
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  • 7. XDH gene mutation is the underlying cause of classical xanthinuria: a second report.
    Levartovsky D, Lagziel A, Sperling O, Liberman U, Yaron M, Hosoya T, Ichida K, Peretz H.
    Kidney Int; 2000 Jun 20; 57(6):2215-20. PubMed ID: 10844591
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  • 8. Using Next-Generation Sequencing to Identify a Mutation in Human MCSU that is Responsible for Type II Xanthinuria.
    Zhou Y, Zhang X, Ding R, Li Z, Hong Q, Wang Y, Zheng W, Geng X, Fan M, Cai G, Chen X, Wu D.
    Cell Physiol Biochem; 2015 Jun 20; 35(6):2412-21. PubMed ID: 25967871
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  • 11. Mutational analysis of the xanthine dehydrogenase gene in a Turkish family with autosomal recessive classical xanthinuria.
    Gok F, Ichida K, Topaloglu R.
    Nephrol Dial Transplant; 2003 Nov 20; 18(11):2278-83. PubMed ID: 14551354
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  • 14. Mutations associated with functional disorder of xanthine oxidoreductase and hereditary xanthinuria in humans.
    Ichida K, Amaya Y, Okamoto K, Nishino T.
    Int J Mol Sci; 2012 Nov 21; 13(11):15475-95. PubMed ID: 23203137
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  • 15. Multi-exon deletion in the XDH gene as a cause of classical xanthinuria.
    Eggermann T, Spengler S, Denecke B, Zerres K, Mache CJ.
    Clin Nephrol; 2013 Jan 21; 79(1):78-80. PubMed ID: 23249873
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  • 16. Molybdenum hydroxylases in Drosophila. II. Molybdenum cofactor in xanthine dehydrogenase, aldehyde oxidase and pyridoxal oxidase.
    Warner CK, Finnerty V.
    Mol Gen Genet; 1981 Jan 21; 184(1):92-6. PubMed ID: 6950197
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  • 17. Thiopurine-induced toxicity is associated with dysfunction variant of the human molybdenum cofactor sulfurase gene (xanthinuria type II).
    Stiburkova B, Pavelcova K, Petru L, Krijt J.
    Toxicol Appl Pharmacol; 2018 Aug 15; 353():102-108. PubMed ID: 29935280
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  • 18. Properties of xanthine dehydrogenase variants from rosy mutant strains of Drosophila melanogaster and their relevance to the enzyme's structure and mechanism.
    Doyle WA, Burke JF, Chovnick A, Dutton FL, Whittle JR, Bray RC.
    Eur J Biochem; 1996 Aug 01; 239(3):782-95. PubMed ID: 8774727
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  • 19. The absence of molybdenum cofactor sulfuration is the primary cause of the flacca phenotype in tomato plants.
    Sagi M, Scazzocchio C, Fluhr R.
    Plant J; 2002 Aug 01; 31(3):305-17. PubMed ID: 12164810
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  • 20. Molybdenum hydroxylases in Drosophila. III. Further characterization of the low xanthine dehydrogenase gene.
    Schott DR, Baldwin MC, Finnerty V.
    Biochem Genet; 1986 Aug 01; 24(7-8):509-27. PubMed ID: 3092803
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