205 related articles for article (PubMed ID: 1678246)
1. Fine structure mapping of the hypoxanthine-guanine phosphoribosyltransferase (HPRT) gene region of the human X chromosome (Xq26).
Nicklas JA; Hunter TC; O'Neill JP; Albertini RJ
Am J Hum Genet; 1991 Aug; 49(2):267-78. PubMed ID: 1678246
[TBL] [Abstract][Full Text] [Related]
2. Multipoint linkage of 9 anonymous probes to HPRT, factor 9, and fragile X.
Brown WT; Ye W; Gross AC; Chan CB; Dobkin CS; Jenkins EC
Am J Med Genet; 1988; 30(1-2):551-66. PubMed ID: 2902796
[TBL] [Abstract][Full Text] [Related]
3. Genetic and physical mapping of Xq24-q26 markers flanking the Lowe oculocerebrorenal syndrome.
Reilly DS; Lewis RA; Nussbaum RL
Genomics; 1990 Sep; 8(1):62-70. PubMed ID: 2081601
[TBL] [Abstract][Full Text] [Related]
4. Analysis of large deletions in the HPRT gene of primary human fibroblasts using the polymerase chain reaction.
Morris T; Masson W; Singleton B; Thacker J
Somat Cell Mol Genet; 1993 Jan; 19(1):9-19. PubMed ID: 8460402
[TBL] [Abstract][Full Text] [Related]
5. Analysis of human HPRT deletion mutations with X-linked probes and pulsed field gel electrophoresis.
Nicklas JA; Lippert MJ; Hunter TC; O'Neill JP; Albertini RJ
Environ Mol Mutagen; 1991; 18(4):270-3. PubMed ID: 1748089
[TBL] [Abstract][Full Text] [Related]
6. Molecular analysis and comparison of radiation-induced large deletions of the HPRT locus in primary human skin fibroblasts.
Yamada Y; Park MS; Okinaka RT; Chen DJ
Radiat Res; 1996 Apr; 145(4):481-90. PubMed ID: 8600509
[TBL] [Abstract][Full Text] [Related]
7. Physical mapping of the human hprt chromosomal region (Xq26).
Lippert MJ; Albertini RJ; Nicklas JA
Mutat Res; 1995 Jan; 326(1):39-49. PubMed ID: 7528884
[TBL] [Abstract][Full Text] [Related]
8. Mapping the end points of large deletions affecting the hprt locus in human peripheral blood cells and cell lines.
Nelson SL; Jones IM; Fuscoe JC; Burkhart-Schultz K; Grosovsky AJ
Radiat Res; 1995 Jan; 141(1):2-10. PubMed ID: 7997511
[TBL] [Abstract][Full Text] [Related]
9. Molecular analyses of in vivo hprt mutations in human T-lymphocytes: IV. Studies in newborns.
McGinniss MJ; Nicklas JA; Albertini RJ
Environ Mol Mutagen; 1989; 14(4):229-37. PubMed ID: 2583130
[TBL] [Abstract][Full Text] [Related]
10. Genetic mapping of two new DNA markers in Xq26-q28 relative to the fragile-X syndrome locus.
Sood R; Mulligan LM; Poon R; White BN; Holden JJ
Am J Hum Genet; 1990 Sep; 47(3):395-402. PubMed ID: 1975476
[TBL] [Abstract][Full Text] [Related]
11. Molecular analyses of in vivo hprt mutations in human T-lymphocytes. III. Longitudinal study of hprt gene structural alterations and T-cell clonal origins.
Nicklas JA; Hunter TC; O'Neill JP; Albertini RJ
Mutat Res; 1989 Dec; 215(2):147-60. PubMed ID: 2557548
[TBL] [Abstract][Full Text] [Related]
12. Acetaldehyde-induced mutation at the hprt locus in human lymphocytes in vitro.
He SM; Lambert B
Environ Mol Mutagen; 1990; 16(2):57-63. PubMed ID: 2209564
[TBL] [Abstract][Full Text] [Related]
13. Southern-blot analyses of human T-lymphocyte mutants induced in vitro by gamma-irradiation.
O'Neill JP; Hunter TC; Sullivan LM; Nicklas JA; Albertini RJ
Mutat Res; 1990 Feb; 240(2):143-9. PubMed ID: 2153929
[TBL] [Abstract][Full Text] [Related]
14. High-resolution mapping of probes near the X-linked lymphoproliferative disease (XLP) locus.
Wu BL; Milunsky A; Nelson D; Schmeckpeper B; Porta G; Schlessinger D; Skare J
Genomics; 1993 Jul; 17(1):163-70. PubMed ID: 8406447
[TBL] [Abstract][Full Text] [Related]
15. High frequency of deletions at the hypoxanthine-guanine phosphoribosyltransferase locus in an ataxia-telangiectasia lymphoblastoid cell line irradiated with gamma-rays.
Tachibana A; Tatsumi K; Furuno-Fukushi I; Sasaki MS
Jpn J Cancer Res; 2001 Nov; 92(11):1190-8. PubMed ID: 11714443
[TBL] [Abstract][Full Text] [Related]
16. Spectrum of point mutations in the coding region of the hypoxanthine-guanine phosphoribosyltransferase (hprt) gene in human T-lymphocytes in vivo.
Podlutsky A; Osterholm AM; Hou SM; Hofmaier A; Lambert B
Carcinogenesis; 1998 Apr; 19(4):557-66. PubMed ID: 9600338
[TBL] [Abstract][Full Text] [Related]
17. Two anonymous X-specific human sequences detecting restriction fragment length polymorphisms in region Xq26----qter.
Boggs BA; Nussbaum RL
Somat Cell Mol Genet; 1984 Nov; 10(6):607-13. PubMed ID: 6095463
[TBL] [Abstract][Full Text] [Related]
18. Karyotypic abnormality of the X chromosome is rare in mutant HPRT-lymphocyte clones.
Muir P; Osborne Y; Morley AA; Turner DR
Mutat Res; 1988 Jan; 197(1):157-60. PubMed ID: 3336373
[TBL] [Abstract][Full Text] [Related]
19. V(D)J recombinase-like activity mediates hprt gene deletion in human fetal T-lymphocytes.
Fuscoe JC; Zimmerman LJ; Lippert MJ; Nicklas JA; O'Neill JP; Albertini RJ
Cancer Res; 1991 Nov; 51(21):6001-5. PubMed ID: 1933863
[TBL] [Abstract][Full Text] [Related]
20. High-resolution cytogenetic analysis of X-ray induced mutations of the HPRT gene of primary human fibroblasts.
Simpson P; Morris T; Savage J; Thacker J
Cytogenet Cell Genet; 1993; 64(1):39-45. PubMed ID: 8508677
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
