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Journal Abstract Search

266 related items for PubMed ID: 7391654

  • 1. Decreased S-adenosylhomocysteine hydrolase in inborn errors of purine metabolism.
    Kaminska JE, Fox IH.
    J Lab Clin Med; 1980 Jul; 96(1):141-7. PubMed ID: 7391654
    [Abstract] [Full Text] [Related]

  • 2. Proposed explanation for S-adenosylhomocysteine hydrolase deficiency in purine nucleoside phosphorylase and hypoxanthine-guanine phosphoribosyltransferase-deficient patients.
    Hershfield MS.
    J Clin Invest; 1981 Mar; 67(3):696-701. PubMed ID: 6782120
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  • 3.
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  • 4. S-adenosylhomocysteine hydrolase activity in defects of enzymes of purine metabolism and inhibition by various purine compounds.
    Chaléon J, Pérignon JL, Hamet M, Cartier PH.
    Adv Exp Med Biol; 1984 Mar; 165 Pt B():71-4. PubMed ID: 6720453
    [No Abstract] [Full Text] [Related]

  • 5. Hypoxanthine-guanine phosphoribosyltransferase: characteristics of the mutant enzyme in erythrocytes from patients with the Lesch-Nyhan syndrome.
    Arnold WJ, Meade JC, Kelley WN.
    J Clin Invest; 1972 Jul; 51(7):1805-12. PubMed ID: 4624352
    [Abstract] [Full Text] [Related]

  • 6. S-Adenosylhomocysteine hydrolase activity in a lymphoblastoid cell line from a patient with adenosine deaminase dificiency disease.
    Tsuchiya S, Nakae S, Konno T, Tada K.
    J Inherit Metab Dis; 1981 Jul; 4(4):197-201. PubMed ID: 6796770
    [Abstract] [Full Text] [Related]

  • 7. Effect of 2'-deoxycoformycin infusion on S-adenosylhomocysteine hydrolase and the amount of S-adenosylhomocysteine and related compounds in tissues of mice.
    Helland S, Ueland PM.
    Cancer Res; 1983 Sep; 43(9):4142-7. PubMed ID: 6603264
    [Abstract] [Full Text] [Related]

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

  • 9. Pharmacological and biochemical aspects of S-adenosylhomocysteine and S-adenosylhomocysteine hydrolase.
    Ueland PM.
    Pharmacol Rev; 1982 Sep; 34(3):223-53. PubMed ID: 6760211
    [No Abstract] [Full Text] [Related]

  • 10. EHNA is a poor inhibitor of deoxyadenosine catabolism in cultured human lymphocytes.
    Goday A, Simmonds HA, Webster DR, Morris GS.
    Rev Esp Fisiol; 1985 Mar; 41(1):49-54. PubMed ID: 3923578
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  • 12. Hypoxanthine-guanine phosphoribosyltransferase deficiency in the Lesch-Nyhan syndrome and gout.
    Kelley WN.
    Fed Proc; 1968 Mar; 27(4):1047-52. PubMed ID: 5658470
    [No Abstract] [Full Text] [Related]

  • 13. Disorders associated with purine and pyrimidine metabolism.
    Edwards NL, Fox IH.
    Spec Top Endocrinol Metab; 1984 Mar; 6():95-140. PubMed ID: 6098039
    [Abstract] [Full Text] [Related]

  • 14. The effect of aliphatic adenine analogues on S-adenosylhomocysteine and S-adenosylhomocysteine hydrolase in intact rat hepatocytes.
    Schanche JS, Schanche T, Ueland PM, Holý A, Votruba I.
    Mol Pharmacol; 1984 Nov; 26(3):553-8. PubMed ID: 6493210
    [Abstract] [Full Text] [Related]

  • 15. The spectrum of hypoxanthine-guanine phosphoribosyltransferase deficiency.
    Emmerson BT, Thompson L.
    Q J Med; 1973 Apr; 42(166):423-40. PubMed ID: 4785440
    [No Abstract] [Full Text] [Related]

  • 16. Purine excretion by cultured skin fibroblasts from patients with abnormal purine metabolism.
    Holland MJ, Klein NC, Cox RP, Dancis J.
    Res Commun Chem Pathol Pharmacol; 1976 Jun; 14(2):331-42. PubMed ID: 940964
    [Abstract] [Full Text] [Related]

  • 17. Combined immunodeficiency disease: an inborn error of purine metabolism.
    Pollara B, Moore JJ, Pickering RJ, Gabrielsen AE, Meuwissen HJ.
    Birth Defects Orig Artic Ser; 1975 Jun; 11(1):120-3. PubMed ID: 1148376
    [Abstract] [Full Text] [Related]

  • 18. Partial deficiency of purine nucleoside phosphorylase: studies of purine and pyrimidine metabolism.
    Edwards NL, Gelfand EW, Biggar D, Fox IH.
    J Lab Clin Med; 1978 May; 91(5):736-49. PubMed ID: 417142
    [No Abstract] [Full Text] [Related]

  • 19. Adenine phosphoribosyltransferase in patients with disorders of purine and pyrimidine metabolism.
    Wilson JM, Daddona PE, Otoadese T, Kelley WN.
    J Lab Clin Med; 1982 Feb; 99(2):163-74. PubMed ID: 7061917
    [Abstract] [Full Text] [Related]

  • 20. Pediatric neurological syndromes and inborn errors of purine metabolism.
    Camici M, Micheli V, Ipata PL, Tozzi MG.
    Neurochem Int; 2010 Feb; 56(3):367-78. PubMed ID: 20005278
    [Abstract] [Full Text] [Related]

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