144 related articles for article (PubMed ID: 1682803)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
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. High-frequency deletion event at aprt locus of CHO cells: detection and characterization of endpoints.
Dewyse P; Bradley WE
Somat Cell Mol Genet; 1989 Jan; 15(1):19-28. PubMed ID: 2916161
[TBL] [Abstract][Full Text] [Related]
8. Analysis of second-step mutations of class II and class III CHO aprt heterozygotes: chromosomal differences in deletion frequencies.
Belouchi A; Bradley WE
Somat Cell Mol Genet; 1991 May; 17(3):277-86. PubMed ID: 1675490
[TBL] [Abstract][Full Text] [Related]
9. Loss of heterozygosity: the most frequent cause of recessive phenotype expression at the heterozygous human adenine phosphoribosyltransferase locus.
Zhu Y; Stambrook PJ; Tischfield JA
Mol Carcinog; 1993; 8(3):138-44. PubMed ID: 8216732
[TBL] [Abstract][Full Text] [Related]
10. Loss of alleles in aprt mutants of CHO cells demonstrated by BclI restriction-fragment-length variation.
Dewyse P; Bradley WE
Somat Cell Mol Genet; 1990 May; 16(3):225-30. PubMed ID: 1972816
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
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. 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]
15. Genetic instability on chromosome 16 in a human B lymphoblastoid cell line.
Smith LE; Grosovsky AJ
Somat Cell Mol Genet; 1993 Nov; 19(6):515-27. PubMed ID: 7907433
[TBL] [Abstract][Full Text] [Related]
16. High-frequency nonrandom mutational event at the adenine phosphoribosyltransferase (aprt) locus of sib-selected CHO variants heterozygous for aprt.
Bradley WE; Letovanec D
Somatic Cell Genet; 1982 Jan; 8(1):51-66. PubMed ID: 7101104
[TBL] [Abstract][Full Text] [Related]
17. Molecular analysis of APRT deficiency in mouse P19 teratocarcinoma stem cell line.
Cooper GE; DiMartino DL; Turker MS
Somat Cell Mol Genet; 1991 Mar; 17(2):105-16. PubMed ID: 2011791
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Characterization of an apparent hotspot for spontaneous mutation in exon 5 of the Chinese hamster APRT gene.
Smith DG; Adair GM
Mutat Res; 1996 Jun; 352(1-2):87-96. PubMed ID: 8676921
[TBL] [Abstract][Full Text] [Related]
20. Cloning of a functional human adenine phosphoribosyltransferase (APRT) gene: identification of a restriction fragment length polymorphism and preliminary analysis of DNAs from APRT-deficient families and cell mutants.
Stambrook PJ; Dush MK; Trill JJ; Tischfield JA
Somat Cell Mol Genet; 1984 Jul; 10(4):359-67. PubMed ID: 6087472
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]