397 related articles for article (PubMed ID: 6326107)
1. Structure, expression, and mutation of the hypoxanthine phosphoribosyltransferase gene.
Melton DW; Konecki DS; Brennand J; Caskey CT
Proc Natl Acad Sci U S A; 1984 Apr; 81(7):2147-51. PubMed ID: 6326107
[TBL] [Abstract][Full Text] [Related]
2. Hypoxanthine-guanine phosphoribosyltransferase genes of mouse and Chinese hamster: construction and sequence analysis of cDNA recombinants.
Konecki DS; Brennand J; Fuscoe JC; Caskey CT; Chinault AC
Nucleic Acids Res; 1982 Nov; 10(21):6763-75. PubMed ID: 6294614
[TBL] [Abstract][Full Text] [Related]
3. The organization of the human HPRT gene.
Kim SH; Moores JC; David D; Respess JG; Jolly DJ; Friedmann T
Nucleic Acids Res; 1986 Apr; 14(7):3103-18. PubMed ID: 3008106
[TBL] [Abstract][Full Text] [Related]
4. Fine structure of the human hypoxanthine phosphoribosyltransferase gene.
Patel PI; Framson PE; Caskey CT; Chinault AC
Mol Cell Biol; 1986 Feb; 6(2):393-403. PubMed ID: 3023844
[TBL] [Abstract][Full Text] [Related]
5. In vitro translation of hypoxanthine/guanine phosphoribosyltransferase mRNA: characterization of a mouse neuroblastoma cell line that has elevated levels of hypoxanthine/guanine phosphoribosyltransferase protein.
Melton DW; Konecki DS; Ledbetter DH; Hejtmancik JF; Caskey CT
Proc Natl Acad Sci U S A; 1981 Nov; 78(11):6977-80. PubMed ID: 6947270
[TBL] [Abstract][Full Text] [Related]
6. The Chinese hamster HPRT gene: restriction map, sequence analysis, and multiplex PCR deletion screen.
Rossiter BJ; Fuscoe JC; Muzny DM; Fox M; Caskey CT
Genomics; 1991 Feb; 9(2):247-56. PubMed ID: 2004774
[TBL] [Abstract][Full Text] [Related]
7. Organization of the HPRT gene and related sequences in the human genome.
Patel PI; Nussbaum RL; gramson PE; Ledbetter DH; Caskey CT; Chinault AC
Somat Cell Mol Genet; 1984 Sep; 10(5):483-93. PubMed ID: 6089358
[TBL] [Abstract][Full Text] [Related]
8. A transmissible retrovirus expressing human hypoxanthine phosphoribosyltransferase (HPRT): gene transfer into cells obtained from humans deficient in HPRT.
Miller AD; Jolly DJ; Friedmann T; Verma IM
Proc Natl Acad Sci U S A; 1983 Aug; 80(15):4709-13. PubMed ID: 6308645
[TBL] [Abstract][Full Text] [Related]
9. Characterization of hprt splicing mutations induced by the ultimate carcinogenic metabolite of benzo[a]pyrene in Chinese hamster V-79 cells.
Hennig EE; Conney AH; Wei SJ
Cancer Res; 1995 Apr; 55(7):1550-8. PubMed ID: 7882364
[TBL] [Abstract][Full Text] [Related]
10. CpG island promoter region methylation patterns of the inactive-X-chromosome hypoxanthine phosphoribosyltransferase (Hprt) gene.
Park JG; Chapman VM
Mol Cell Biol; 1994 Dec; 14(12):7975-83. PubMed ID: 7969137
[TBL] [Abstract][Full Text] [Related]
11. A three-allele restriction-fragment-length polymorphism at the hypoxanthine phosphoribosyltransferase locus in man.
Nussbaum RL; Crowder WE; Nyhan WL; Caskey CT
Proc Natl Acad Sci U S A; 1983 Jul; 80(13):4035-9. PubMed ID: 6306659
[TBL] [Abstract][Full Text] [Related]
12. Cloned cDNA sequences of the hypoxanthine/guanine phosphoribosyltransferase gene from a mouse neuroblastoma cell line found to have amplified genomic sequences.
Brennand J; Chinault AC; Konecki DS; Melton DW; Caskey CT
Proc Natl Acad Sci U S A; 1982 Mar; 79(6):1950-4. PubMed ID: 6952245
[TBL] [Abstract][Full Text] [Related]
13. Induced reversion of a spontaneous point mutation within the Chinese hamster HPRT gene to the wild-type sequence.
Rossiter BJ; Muzny DM; Hampson I; Caskey CT; Fox M
Mutagenesis; 1990 Nov; 5(6):605-8. PubMed ID: 1702179
[TBL] [Abstract][Full Text] [Related]
14. Resolution of a missense mutant in human genomic DNA by denaturing gradient gel electrophoresis and direct sequencing using in vitro DNA amplification: HPRT Munich.
Cariello NF; Scott JK; Kat AG; Thilly WG; Keohavong P
Am J Hum Genet; 1988 May; 42(5):726-34. PubMed ID: 3358423
[TBL] [Abstract][Full Text] [Related]
15. The gene encoding hypoxanthine-guanine phosphoribosyltransferase as target for mutational analysis: PCR cloning and sequencing of the cDNA from the rat.
Jansen JG; Vrieling H; van Zeeland AA; Mohn GR
Mutat Res; 1992 Apr; 266(2):105-16. PubMed ID: 1373820
[TBL] [Abstract][Full Text] [Related]
16. Isolation and characterization of a full-length expressible cDNA for human hypoxanthine phosphoribosyl transferase.
Jolly DJ; Okayama H; Berg P; Esty AC; Filpula D; Bohlen P; Johnson GG; Shively JE; Hunkapillar T; Friedmann T
Proc Natl Acad Sci U S A; 1983 Jan; 80(2):477-81. PubMed ID: 6300847
[TBL] [Abstract][Full Text] [Related]
17. Predicted changes in pre-mRNA secondary structure vary in their association with exon skipping for mutations in exons 2, 4, and 8 of the Hprt gene and exon 51 of the fibrillin gene.
Tu M; Tong W; Perkins R; Valentine CR
Mutat Res; 2000 Feb; 432(1-2):15-32. PubMed ID: 10729708
[TBL] [Abstract][Full Text] [Related]
18. A method for specific cloning and sequencing of human hprt cDNA for mutation analysis.
Simpson D; Crosby RM; Skopek TR
Biochem Biophys Res Commun; 1988 Feb; 151(1):487-92. PubMed ID: 3348790
[TBL] [Abstract][Full Text] [Related]
19. Activation of a nonexpressed hypoxanthine phosphoribosyltransferase allele in mutant H23 HeLa cells by agents that inhibit DNA methylation.
Ivarie R; Morris JA
Mol Cell Biol; 1986 Jan; 6(1):97-104. PubMed ID: 2431268
[TBL] [Abstract][Full Text] [Related]
20. Novel nonsense mutation in the hypoxanthine guanine phosphoribosyltransferase gene and nonrandom X-inactivation causing Lesch-Nyhan syndrome in a female patient.
Aral B; de Saint Basile G; Al-Garawi S; Kamoun P; Ceballos-Picot I
Hum Mutat; 1996; 7(1):52-8. PubMed ID: 8664901
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
