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Journal Abstract Search

140 related items for PubMed ID: 1682803

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  • 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
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  • 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
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  • 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
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  • 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 May; 8(3):138-44. PubMed ID: 8216732
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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 28; 358(1):89-96. PubMed ID: 8921979
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  • 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 10; 352(1-2):87-96. PubMed ID: 8676921
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  • 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; 10(4):359-67. PubMed ID: 6087472
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