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Journal Abstract Search

123 related items for PubMed ID: 3955845

  • 1. 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
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  • 5. Selection against blood cells deficient in hypoxanthine phosphoribosyltransferase (HPRT) in Lesch-Nyhan heterozygotes occurs at the level of multipotent stem cells.
    Hakoda M, Hirai Y, Akiyama M, Yamanaka H, Terai C, Kamatani N, Kashiwazaki S.
    Hum Genet; 1995 Dec 15; 96(6):674-80. PubMed ID: 8522326
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  • 9. Genetic heterogeneity of hypoxanthine-phosphoribosyl transferase in human fibroblasts of 3 families.
    Willers I, Held KR, Singh S, Goedde HW.
    Clin Genet; 1977 Mar 15; 11(3):193-200. PubMed ID: 837570
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  • 10. Molecular and tissue-specific heterogeneity in HPRT deficiency.
    Uitendaal MP, de Bruyn CH, Oei TL, Hösli P.
    Biochem Genet; 1978 Dec 15; 16(11-12):1187-202. PubMed ID: 571718
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  • 11. Human hypoxanthine-guanine phosphoribosyltransferase: a single nucleotide substitution in cDNA clones isolated from a patient with Lesch-Nyhan syndrome (HPRTMidland).
    Davidson BL, Palella TD, Kelley WN.
    Gene; 1988 Aug 15; 68(1):85-91. PubMed ID: 3265398
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  • 12. High HPRT activity in fibroblasts from patients with Lesch-Nyhan syndrome due to bacterial "L-form" contamination.
    Willers I, Singh S, Held KR, Goedde HW.
    Adv Exp Med Biol; 1980 Aug 15; 122A():327-31. PubMed ID: 7424651
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  • 13. Genetic analysis of the HPRT mutation of Lesch-Nyhan syndrome in a Chinese family.
    Lee WJ, Lee HM, Chi CS, Yang MT, Lin HY, Lin WH.
    Zhonghua Yi Xue Za Zhi (Taipei); 1995 Dec 15; 56(6):359-66. PubMed ID: 8851475
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  • 14. Hypoxanthine-guanine phosphoribosyl transferase regulates early developmental programming of dopamine neurons: implications for Lesch-Nyhan disease pathogenesis.
    Ceballos-Picot I, Mockel L, Potier MC, Dauphinot L, Shirley TL, Torero-Ibad R, Fuchs J, Jinnah HA.
    Hum Mol Genet; 2009 Jul 01; 18(13):2317-27. PubMed ID: 19342420
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  • 16. Prenatal diagnosis of Lesch-Nyhan syndrome and some characteristics of hypoxanthine-guanine phosphoribosyltransferase and adenine phosphoribosyltransferase in human tissues and cultivated cells.
    Shin-Buehring YS, Osang M, Wirtz A, Haas B, Rahm P, Schaub J.
    Pediatr Res; 1980 Jun 01; 14(6):825-9. PubMed ID: 7402756
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  • 17. Adenine phosphoribosyl transferase deficiency in association with sub-normal hypoxanthine phophoribosyl transferase in families of Lesch--Nyhan patients.
    Itiaba K, Melançon SB, Dallaire L, Crawhall JC.
    Biochem Med; 1978 Apr 01; 19(2):252-9. PubMed ID: 656085
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  • 18. Hypoxanthine-guanine phosphoribosyltransferase activity in individual erythrocytes: autoradiographic studies in heterozygotes.
    Emmerson BT, Gordon RB, Johnson LA.
    Ciba Found Symp; 1977 Apr 01; (48):97-104. PubMed ID: 245995
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  • 20. [Investigation of a variant form of hypoxanthine-phosphoribosyl transferase in a family (author's transl)].
    Willers I, Held KR, Singh S, Goedde HW.
    Wien Klin Wochenschr; 1981 May 15; 93(10):329-31. PubMed ID: 7257414
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