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Journal Abstract Search

102 related items for PubMed ID: 3939388

  • 1. Familial hyperlysinemias--multiple enzyme deficiencies associated with the bifunctional aminoadipic semialdehyde synthase.
    Cox RP, Markovitz PJ, Chuang DT.
    Trans Am Clin Climatol Assoc; 1986; 97():69-81. PubMed ID: 3939388
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  • 5. Familial hyperlysinemia: enzyme studies, diagnostic methods, comments on terminology.
    Dancis J, Hutzler J, Cox RP.
    Am J Hum Genet; 1979 May; 31(3):290-9. PubMed ID: 463877
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  • 6. The bifunctional aminoadipic semialdehyde synthase in lysine degradation. Separation of reductase and dehydrogenase domains by limited proteolysis and column chromatography.
    Markovitz PJ, Chuang DT.
    J Biol Chem; 1987 Jul 05; 262(19):9353-8. PubMed ID: 3110158
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  • 7. Familial hyperlysinaemia due to L-lysine alpha-ketoglutarate reductase deficiency: results of attempted treatment.
    vd Heiden C, Brink M, de Bree PK, v Sprang FJ, Wadman SK, de Pater JM, van Biervliet JP.
    J Inherit Metab Dis; 1978 Jul 05; 1(3):89-94. PubMed ID: 116084
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  • 8. Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemia.
    Sacksteder KA, Biery BJ, Morrell JC, Goodman BK, Geisbrecht BV, Cox RP, Gould SJ, Geraghty MT.
    Am J Hum Genet; 2000 Jun 05; 66(6):1736-43. PubMed ID: 10775527
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  • 9. Hyperlysinemia with saccharopinuria due to combined lysine-ketoglutarate reductase and saccharopine dehydrogenase deficiencies presenting as cystinuria.
    Cederbaum SD, Shaw KN, Dancis J, Hutzler J, Blaskovics JC.
    J Pediatr; 1979 Aug 05; 95(2):234-8. PubMed ID: 571908
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  • 10. The catabolic function of the alpha-aminoadipic acid pathway in plants is associated with unidirectional activity of lysine-oxoglutarate reductase, but not saccharopine dehydrogenase.
    Zhu X, Tang G, Galili G.
    Biochem J; 2000 Oct 01; 351(Pt 1):215-20. PubMed ID: 10998364
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  • 13. Glutaric aciduria type II: evidence for a defect related to the electron transfer flavoprotein or its dehydrogenase.
    Christensen E, Kølvraa S, Gregersen N.
    Pediatr Res; 1984 Jul 01; 18(7):663-7. PubMed ID: 6433313
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  • 14. Lysine degradation through the saccharopine pathway in mammals: involvement of both bifunctional and monofunctional lysine-degrading enzymes in mouse.
    Papes F, Kemper EL, Cord-Neto G, Langone F, Arruda P.
    Biochem J; 1999 Dec 01; 344 Pt 2(Pt 2):555-63. PubMed ID: 10567240
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  • 15. Isolated and combined deficiencies of the alpha-keto acid dehydrogenase complexes.
    Robinson BH, Chun K, Mackay N, Otulakowski G, Petrova-Benedict R, Willard H.
    Ann N Y Acad Sci; 1989 Dec 01; 573():337-46. PubMed ID: 2634350
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  • 19. A new type of hyperlysinaemia due to a transport defect of lysine into mitochondria.
    Oyanagi K, Aoyama T, Tsuchiyama A, Nakao T, Uetsuji N, Wagatsuma K, Tsugawa S.
    J Inherit Metab Dis; 1986 Dec 01; 9(3):313-6. PubMed ID: 3099081
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  • 20. Stereospecificity of hydrogen transfer in the saccharopine dehydrogenase reaction.
    Fujioka M, Takata Y.
    Biochim Biophys Acta; 1979 Sep 12; 570(1):210-2. PubMed ID: 226150
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