These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
178 related articles for article (PubMed ID: 5274481)
1. Evidence for transfer of enzyme product as the basis of metabolic cooperation between tissue culture fibroblasts of Lesch-Nyhan disease and normal cells. Cox RP; Krauss MR; Balis ME; Dancis J Proc Natl Acad Sci U S A; 1970 Nov; 67(3):1573-9. PubMed ID: 5274481 [TBL] [Abstract][Full Text] [Related]
5. Activation of variants of hypoxanthine-guanine phosphoribosyl transferase by the normal enzyme. Bakay B; Nyhan WL Proc Natl Acad Sci U S A; 1972 Sep; 69(9):2523-6. PubMed ID: 4341698 [TBL] [Abstract][Full Text] [Related]
7. 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 [TBL] [Abstract][Full Text] [Related]
8. Purine requirement of cells cultured from humans affected with Lesch-Nyhan syndrome (hypoxanthine-guanine phosphoribosyltransferase deficiency). Felix JS; DeMars R Proc Natl Acad Sci U S A; 1969 Feb; 62(2):536-43. PubMed ID: 5256231 [TBL] [Abstract][Full Text] [Related]
9. Purification of IMP:pyrophosphate phosphoribosyltransferases, catalytically incompetent enzymes in Lesch-Nyhan disease. Rubin CS; Dancis J; Yip LC; Nowinski RC; Balis ME Proc Natl Acad Sci U S A; 1971 Jul; 68(7):1461-4. PubMed ID: 4327003 [TBL] [Abstract][Full Text] [Related]
10. Detection of the heterozygote in Lesch-Nyhan disease by hair-root analysis. Silvers DN; Cox RP; Balis ME; Dancis J N Engl J Med; 1972 Feb; 286(8):390-5. PubMed ID: 4333083 [No Abstract] [Full Text] [Related]
11. Detection of females heterozygous for the Lesch-Nyhan mutation by 8-azaguanine-resistant growth of cultured fibroblasts. Felix JS; DeMars R J Lab Clin Med; 1971 Apr; 77(4):596-604. PubMed ID: 4252001 [No Abstract] [Full Text] [Related]
12. Substrate stabilization: genetically-controlled reciprocal relationship between two enzymes. Boyle JA; Green ML; Seegmiller JE Ann Rheum Dis; 1971 May; 30(3):326-7. PubMed ID: 4326237 [No Abstract] [Full Text] [Related]
13. Diagnosis of Lesch-Nyhan syndrome by direct study of skin specimens. Frost P; Weinstein GD; Nyhan WL JAMA; 1970 Apr; 212(2):316-8. PubMed ID: 5467237 [No Abstract] [Full Text] [Related]
17. [Lesch-Nyhan syndrome. Heterozygote detection by biochemical selection of the mutant cells and autoradiography]. Hagemeijer AM; Dodinval P; Andrien JM Humangenetik; 1972; 15(2):126-35. PubMed ID: 5049065 [No Abstract] [Full Text] [Related]
18. Overproduction of uric acid in hypoxanthine-guanine phosphoribosyltransferase deficiency. Contribution by impaired purine salvage. Edwards NL; Recker D; Fox IH J Clin Invest; 1979 May; 63(5):922-30. PubMed ID: 447834 [TBL] [Abstract][Full Text] [Related]
19. Further studies of the enzyme composition of mutant cells in X-linked uric aciduria. Sweetman L; Nyhan WL Arch Intern Med; 1972 Aug; 130(2):214-20. PubMed ID: 5065734 [No Abstract] [Full Text] [Related]
20. Hypoxanthine-guanine phosphoribosyltransferase deficiency: chemical agents selective for mutant or normal cultured fibroblasts in mixed and heterozygote cultures. Fujimoto WY; Subak-Sharpe JH; Seegmiller JE Proc Natl Acad Sci U S A; 1971 Jul; 68(7):1516-9. PubMed ID: 5283941 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]