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Journal Abstract Search

147 related items for PubMed ID: 220971

  • 21. Purine synthesis during amino acid starvation of lymphoblasts with HPRT deficiency or PP-ribose-P synthetase overactivity decreases less than in normal cells.
    Boss GR.
    Adv Exp Med Biol; 1984; 165 Pt B():15-9. PubMed ID: 6326498
    [No Abstract] [Full Text] [Related]

  • 22. [Simple microlitre-method for the determination of hypoxanthine-guanine-phosphoribosyl transferase activity in erythrocytes and skin fibroblasts].
    Grimm U, Lubs H, Machill G, Weber A, Knapp A, Stareprawo G.
    Acta Biol Med Ger; 1974; 33(4):507-10. PubMed ID: 4466293
    [No Abstract] [Full Text] [Related]

  • 23.
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  • 24. Genetic heterogeneity of hypoxanthine-phosphoribosyl transferase in human fibroblasts of 3 families.
    Willers I, Held KR, Singh S, Goedde HW.
    Clin Genet; 1977 Mar; 11(3):193-200. PubMed ID: 837570
    [Abstract] [Full Text] [Related]

  • 25. Use of selective media for distinguishing variant forms of hypoxanthine phosphoribosyl transferase.
    Page TM, Broock RL, Nyhan WL, Nieto LH.
    Clin Chim Acta; 1986 Feb 15; 154(3):195-201. PubMed ID: 3955845
    [Abstract] [Full Text] [Related]

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  • 27. Monoamine oxidase activity decreased in cells lacking hypoxanthine phosphoribosyltransferase activity.
    Breakefield XO, Castiglione CM, Edelstein SB.
    Science; 1976 Jun 04; 192(4243):1018-20. PubMed ID: 1273584
    [Abstract] [Full Text] [Related]

  • 28. Production of a model for Lesch-Nyhan syndrome in hypoxanthine phosphoribosyltransferase-deficient mice.
    Wu CL, Melton DW.
    Nat Genet; 1993 Mar 04; 3(3):235-40. PubMed ID: 8485579
    [Abstract] [Full Text] [Related]

  • 29.
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  • 30. Inherited hyperuricemic disorders.
    Nyhan WL.
    Contrib Nephrol; 2005 Mar 04; 147():22-34. PubMed ID: 15604603
    [Abstract] [Full Text] [Related]

  • 31. Abnormalities in cellular adhesion of neuroblastoma and fibroblast models of Lesch Nyhan syndrome.
    Stacey NC, Ma MH, Duley JA, Connolly GP.
    Neuroscience; 2000 Mar 04; 98(2):397-401. PubMed ID: 10854773
    [Abstract] [Full Text] [Related]

  • 32. Increased PRPP synthetase activity in cultured rat hepatoma cells containing mutations in the hypoxanthine-guanine phosphoribosyltransferase gene.
    Graf LH, McRoberts JA, Harrison TM, Martin DW.
    J Cell Physiol; 1976 Jul 04; 88(3):331-42. PubMed ID: 178676
    [Abstract] [Full Text] [Related]

  • 33. Preimplantation diagnosis of deficiency of hypoxanthine phosphoribosyl transferase in a mouse model for Lesch-Nyhan syndrome.
    Monk M, Handyside A, Hardy K, Whittingham D.
    Lancet; 1987 Aug 22; 2(8556):423-5. PubMed ID: 2887727
    [Abstract] [Full Text] [Related]

  • 34. Purine biosynthesis in mutant mammalian cells.
    Reem GH.
    Ciba Found Symp; 1977 Aug 22; (48):105-26. PubMed ID: 204459
    [Abstract] [Full Text] [Related]

  • 35. [Hereditary anomalies of purine metabolism. Current biochemical aspects].
    Perignon JL, Cartier P.
    Arch Fr Pediatr; 1980 Oct 22; 37(8):487-90. PubMed ID: 6255885
    [No Abstract] [Full Text] [Related]

  • 36. Metabolic cooperation between human fibroblasts with normal and with mutant superactive phosphoribosylpyrophosphate synthetase.
    Zoref E, De Vries A, Sperling O.
    Nature; 1976 Apr 29; 260(5554):787-8. PubMed ID: 177888
    [No Abstract] [Full Text] [Related]

  • 37.
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  • 38. Regional localization of the gene for human phosphoribosylpyrophosphate synthetase on the X chromosome.
    Becker MA, Yen RC, Itkin P, Goss SJ, Seegmiller JE, Bakay B.
    Science; 1979 Mar 09; 203(4384):1016-9. PubMed ID: 218284
    [Abstract] [Full Text] [Related]

  • 39. [Activity of erythrocyte purine phosphoribosyltransferases in Lesch-Nyhan syndrome].
    Aleksandrova LA, Shaposhnikov AM.
    Vopr Med Khim; 1981 Mar 09; 27(2):215-20. PubMed ID: 7281560
    [Abstract] [Full Text] [Related]

  • 40.
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