6440 related articles for article (PubMed ID: 1688803)
1. Levels of hypoxanthine phosphoribosyltransferase RNA in human cells.
Steen AM; Luthman H; Hellgren D; Lambert B
Exp Cell Res; 1990 Feb; 186(2):236-44. PubMed ID: 1688803
[TBL] [Abstract][Full Text] [Related]
2. Expression of the hypoxanthine phosphoribosyl transferase gene in resting and growth-stimulated human lymphocytes.
Steen AM; Sahlén S; Lambert B
Biochim Biophys Acta; 1991 Jan; 1088(1):77-85. PubMed ID: 1703446
[TBL] [Abstract][Full Text] [Related]
3. Lesch-Nyhan syndrome: mRNA expression of HPRT in patients with enzyme proven deficiency of HPRT and normal HPRT coding region of the DNA.
Nguyen KV; Naviaux RK; Paik KK; Nyhan WL
Mol Genet Metab; 2012 Aug; 106(4):498-501. PubMed ID: 22766437
[TBL] [Abstract][Full Text] [Related]
4. 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; 96(6):674-80. PubMed ID: 8522326
[TBL] [Abstract][Full Text] [Related]
5. Studies in fibroblasts of patients with the Lesch-Nyhan syndrome and HPRT variants. Correlation of HPRT activity with hypoxanthine utilization and growth in selection media.
Willers I; Singh S; Goedde HW
Enzyme; 1984; 32(4):241-7. PubMed ID: 6526001
[TBL] [Abstract][Full Text] [Related]
6. Autoradiographic detection of HPRT variants of human lymphocytes resistant to RNA synthesis inhibition.
Jones IM; Zetterberg G; Strout CL; Carrano AV
Mutat Res; 1985 Mar; 149(1):133-40. PubMed ID: 2579332
[TBL] [Abstract][Full Text] [Related]
7. Characterization of mutations in phenotypic variants of hypoxanthine phosphoribosyltransferase deficiency.
Sege-Peterson K; Chambers J; Page T; Jones OW; Nyhan WL
Hum Mol Genet; 1992 Sep; 1(6):427-32. PubMed ID: 1301916
[TBL] [Abstract][Full Text] [Related]
8. Hprt activities and RNA phenotypes in 6-thioguanine resistant human T-lymphocytes.
Steen AM; Sahlén S; Hou SM; Lambert B
Mutat Res; 1993 Apr; 286(2):209-15. PubMed ID: 7681532
[TBL] [Abstract][Full Text] [Related]
9. Altered membrane NTPase activity in Lesch-Nyhan disease fibroblasts: comparison with HPRT knockout mice and HPRT-deficient cell lines.
Pinto CS; Jinnah HA; Shirley TL; Nyhan WL; Seifert R
J Neurochem; 2005 Jun; 93(6):1579-86. PubMed ID: 15935074
[TBL] [Abstract][Full Text] [Related]
10. A molecular survey of hypoxanthine-guanine phosphoribosyltransferase deficiency in man.
Wilson JM; Stout JT; Palella TD; Davidson BL; Kelley WN; Caskey CT
J Clin Invest; 1986 Jan; 77(1):188-95. PubMed ID: 3944251
[TBL] [Abstract][Full Text] [Related]
11. Molecular analyses of a Lesch-Nyhan syndrome mutation (hprtMontreal) by use of T-lymphocyte cultures.
Skopek TR; Recio L; Simpson D; Dallaire L; Melancon SB; Ogier H; O'Neill JP; Falta MT; Nicklas JA; Albertini RJ
Hum Genet; 1990 Jun; 85(1):111-6. PubMed ID: 2358296
[TBL] [Abstract][Full Text] [Related]
12. Expression of SV40 large T antigen stimulates reversion of a chromosomal gene duplication in human cells.
Cheng RZ; Shammas MA; Li J; Shmookler Reis RJ
Exp Cell Res; 1997 Aug; 234(2):300-12. PubMed ID: 9260898
[TBL] [Abstract][Full Text] [Related]
13. Expression of human and Chinese hamster hypoxanthine-guanine phosphoribosyltransferase cDNA recombinants in cultured Lesch-Nyhan and Chinese hamster fibroblasts.
Brennand J; Konecki DS; Caskey CT
J Biol Chem; 1983 Aug; 258(16):9593-6. PubMed ID: 6688416
[TBL] [Abstract][Full Text] [Related]
14. 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; 56(6):359-66. PubMed ID: 8851475
[TBL] [Abstract][Full Text] [Related]
15. 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; 68(1):85-91. PubMed ID: 3265398
[TBL] [Abstract][Full Text] [Related]
16. Molecular analysis of hypoxanthine guanine phosphoribosyltransferase (HPRT) deficiencies: novel mutations and the spectrum of Japanese mutations.
Yamada Y; Nomura N; Yamada K; Wakamatsu N; Kaneko K; Fujimori S
Nucleosides Nucleotides Nucleic Acids; 2008 Jun; 27(6):570-4. PubMed ID: 18600506
[TBL] [Abstract][Full Text] [Related]
17. Alterations of the hprt gene in human in vivo-derived 6-thioguanine-resistant T lymphocytes.
Albertini RJ; O'Neill JP; Nicklas JA; Heintz NH; Kelleher PC
Nature; 1985 Jul 25-31; 316(6026):369-71. PubMed ID: 2991767
[TBL] [Abstract][Full Text] [Related]
18. Hypoxanthine-guanine phosphoribosyltransferase in human lymphoblastoid cells: confirmation of four structural variants and demonstration of a new variant (HPRT Ann Arbor).
Wilson JM; Baugher BW; Kelley WN
Adv Exp Med Biol; 1984; 165 Pt B():33-8. PubMed ID: 6720433
[No Abstract] [Full Text] [Related]
19. The molecular characterisation of HPRT CHERMSIDE and HPRT COORPAROO: two Lesch-Nyhan patients with reduced amounts of mRNA.
Gordon RB; Dawson PA; Sculley DG; Emmerson BT; Caskey CT; Gibbs RA
Gene; 1991 Dec; 108(2):299-304. PubMed ID: 1840549
[TBL] [Abstract][Full Text] [Related]
20. The spectrum of inherited mutations causing HPRT deficiency: 75 new cases and a review of 196 previously reported cases.
Jinnah HA; De Gregorio L; Harris JC; Nyhan WL; O'Neill JP
Mutat Res; 2000 Oct; 463(3):309-26. PubMed ID: 11018746
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
