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8. Comparative EPR and redox studies of three prokaryotic enzymes of the xanthine oxidase family: quinoline 2-oxidoreductase, quinaldine 4-oxidase, and isoquinoline 1-oxidoreductase. Canne C; Stephan I; Finsterbusch J; Lingens F; Kappl R; Fetzner S; Hüttermann J Biochemistry; 1997 Aug; 36(32):9780-90. PubMed ID: 9245410 [TBL] [Abstract][Full Text] [Related]
9. Quantitative transfer of the molybdenum cofactor from xanthine oxidase and from sulphite oxidase to the deficient enzyme of the nit-1 mutant of Neurospora crassa to yield active nitrate reductase. Hawkes TR; Bray RC Biochem J; 1984 Apr; 219(2):481-93. PubMed ID: 6234882 [TBL] [Abstract][Full Text] [Related]
10. Molybdenum in enzymatic and heterogeneous catalysis. Mitchell PC J Inorg Biochem; 1986; 28(2-3):107-23. PubMed ID: 3806088 [TBL] [Abstract][Full Text] [Related]
11. 17O ESEEM evidence for exchange of the axial oxo ligand in the molybdenum center of the high pH form of sulfite oxidase. Astashkin AV; Feng C; Raitsimring AM; Enemark JH J Am Chem Soc; 2005 Jan; 127(2):502-3. PubMed ID: 15643856 [TBL] [Abstract][Full Text] [Related]
13. Simultaneous occurrence of xanthine oxidase and sulfite oxidase deficiency. A molybdenum dependent inborn error of metabolism? van der Heiden C; Beemer FA; Brink W; Wadman SK; Duran M Clin Biochem; 1979 Dec; 12(6):206-8. PubMed ID: 583402 [TBL] [Abstract][Full Text] [Related]
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17. Investigation of metal-dithiolate fold angle effects: implications for molybdenum and tungsten enzymes. Joshi HK; Cooney JJ; Inscore FE; Gruhn NE; Lichtenberger DL; Enemark JH Proc Natl Acad Sci U S A; 2003 Apr; 100(7):3719-24. PubMed ID: 12655066 [TBL] [Abstract][Full Text] [Related]
18. Combined deficiency of xanthine oxidase and sulphite oxidase: a defect of molybdenum metabolism or transport? Duran M; Beemer FA; van de Heiden C; Korteland J; de Bree PK; Brink M; Wadman SK; Lombeck I J Inherit Metab Dis; 1978; 1(4):175-8. PubMed ID: 117254 [TBL] [Abstract][Full Text] [Related]
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20. [Double deficiency of sulfite and xanthine oxidase causing encephalopathy and due to a hereditary anomaly in the metabolism of molybdenum]. Ogier H; Saudubray JM; Charpentier C; Munnich A; Perignon JL; Kesseler A; Frezal J Ann Med Interne (Paris); 1982; 133(8):594-6. PubMed ID: 6897810 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]