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.
145 related articles for article (PubMed ID: 1381471)
1. Allelic losses in mutations at the aprt locus of human lymphoblastoid cells. Fujimori A; Tachibana A; Tatsumi K Mutat Res; 1992 Sep; 269(1):55-62. PubMed ID: 1381471 [TBL] [Abstract][Full Text] [Related]
2. Evidence for high-frequency allele loss at the aprt locus in TK6 human lymphoblasts. Smith LE; Grosovsky AJ Mutat Res; 1993 Oct; 289(2):245-54. PubMed ID: 7690893 [TBL] [Abstract][Full Text] [Related]
3. Reduction to homozygosity is the predominant spontaneous mutational event in cultured human lymphoblastoid cells. Klinedinst DK; Drinkwater NR Mutat Res; 1991; 250(1-2):365-74. PubMed ID: 1682803 [TBL] [Abstract][Full Text] [Related]
4. The nature of ultraviolet light-induced mutations at the heterozygous aprt locus in Chinese hamster ovary cells. Drobetsky EA; Glickman BW Mutat Res; 1990 Oct; 232(2):281-9. PubMed ID: 1977078 [TBL] [Abstract][Full Text] [Related]
5. Mutagenicity and loss of heterozygosity at the APRT locus in human lymphoblastoid cells exposed to 3'-azido-3'-deoxythymidine. Meng Q; Grosovsky AJ; Shi X; Walker VE Mutagenesis; 2000 Sep; 15(5):405-10. PubMed ID: 10970446 [TBL] [Abstract][Full Text] [Related]
6. Loss of heterozygosity in mammalian cell mutagenesis: molecular analysis of spontaneous mutations at the aprt locus in CHO cells. Ward MA; Yu M; Glickman BW; Grosovsky AJ Carcinogenesis; 1990 Sep; 11(9):1485-90. PubMed ID: 1976045 [TBL] [Abstract][Full Text] [Related]
7. Intervention of somatic mutational events in vivo by a germline defect at the adenine phosphoribosyltransferase locus. Hakoda M; Kamatani N; Kurumada S; Hirai Y; Sakamoto K; Yamanaka H; Terai C; Kashiwazaki S Hum Genet; 1997 Feb; 99(2):164-70. PubMed ID: 9048914 [TBL] [Abstract][Full Text] [Related]
8. Isolation of an APRT heterozygote from TK6 human lymphoblasts: predominance of multi-locus loss of heterozygosity among spontaneous APRT-mutants. Pongsaensook P; Smith LE; Grosovsky AJ Mutat Res; 1997 Jun; 377(1):27-36. PubMed ID: 9219576 [TBL] [Abstract][Full Text] [Related]
9. Structure of mutant alleles at the aprt locus of Chinese hamster ovary cells. Nalbantoglu J; Goncalves O; Meuth M J Mol Biol; 1983 Jul; 167(3):575-94. PubMed ID: 6308265 [TBL] [Abstract][Full Text] [Related]
10. Heritable alterations at the adenine phosphoribosyltransferase (APRT) locus in human lymphoblastoid cell lines. Amundson SA; Fortunato JE; Liber HL Mutat Res; 1992 Dec; 284(2):287-95. PubMed ID: 1281280 [TBL] [Abstract][Full Text] [Related]
11. Mutations causing deficiency of APRT in fibroblasts cultured from human heterozygous for mutant APRT alleles. Steglich C; DeMars R Somatic Cell Genet; 1982 Jan; 8(1):115-41. PubMed ID: 7101101 [TBL] [Abstract][Full Text] [Related]
12. Only three mutations account for almost all defective alleles causing adenine phosphoribosyltransferase deficiency in Japanese patients. Kamatani N; Hakoda M; Otsuka S; Yoshikawa H; Kashiwazaki S J Clin Invest; 1992 Jul; 90(1):130-5. PubMed ID: 1353080 [TBL] [Abstract][Full Text] [Related]
13. Spontaneous and ionizing radiation induced mutations involve large events when selecting for loss of an autosomal locus. Turker M; Walker KA; Jennings CD; Mellon I; Yusufji A; Urano M Mutat Res; 1995 Jul; 329(2):97-105. PubMed ID: 7603506 [TBL] [Abstract][Full Text] [Related]
14. Benzo[a]pyrenediol-epoxide induces loss of heterozygosity in Chinese hamster ovary cells heterozygous at the aprt locus. Mazur-Melnyk M; Stuart GR; Glickman BW Mutat Res; 1996 Oct; 358(1):89-96. PubMed ID: 8921979 [TBL] [Abstract][Full Text] [Related]
15. High rate of multilocus deletion in a human tumor cell line. Harwood J; Tachibana A; Davis R; Bhattacharyya NP; Meuth M Hum Mol Genet; 1993 Feb; 2(2):165-71. PubMed ID: 8499904 [TBL] [Abstract][Full Text] [Related]
16. APRT: a versatile in vivo resident reporter of local mutation and loss of heterozygosity. Stambrook PJ; Shao C; Stockelman M; Boivin G; Engle SJ; Tischfield JA Environ Mol Mutagen; 1996; 28(4):471-82. PubMed ID: 8991080 [TBL] [Abstract][Full Text] [Related]
17. Selection of human cells having two different types of mutations in individual cells (genetic/artificial mutants). Application to the diagnosis of the heterozygous state for a type of adenine phosphoribosyltransferase deficiency. Kamatani N; Kuroshima S; Terai C; Kawai K; Mikanagi K; Nishioka K Hum Genet; 1987 Jun; 76(2):148-52. PubMed ID: 3610146 [TBL] [Abstract][Full Text] [Related]
18. Determination of spontaneous loss of heterozygosity mutations in Aprt heterozygous mice. Van Sloun PP; Wijnhoven SW; Kool HJ; Slater R; Weeda G; van Zeeland AA; Lohman PH; Vrieling H Nucleic Acids Res; 1998 Nov; 26(21):4888-94. PubMed ID: 9776749 [TBL] [Abstract][Full Text] [Related]
19. High-frequency structural gene deletion as the basis for functional hemizygosity of the adenine phosphoribosyltransferase locus in Chinese hamster ovary cells. Adair GM; Stallings RL; Nairn RS; Siciliano MJ Proc Natl Acad Sci U S A; 1983 Oct; 80(19):5961-4. PubMed ID: 6310607 [TBL] [Abstract][Full Text] [Related]
20. DNA sequence determination of gamma-radiation-induced mutations of the hamster aprt locus. Miles C; Meuth M Mutat Res; 1989 Oct; 227(2):97-102. PubMed ID: 2797048 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]