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Journal Abstract Search

130 related items for PubMed ID: 1972816

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Spontaneous CHO APRT heterozygotes reflect high-frequency, allele-specific deletion of the chromosome Z4 APRT gene.
    Adair GM, Nairn RS, Brotherman KA, Siciliano MJ.
    Somat Cell Mol Genet; 1989 Nov; 15(6):535-44. PubMed ID: 2595453
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Preferential loss or inactivation of chromosome Z4 APRT allele in CHO cells.
    Adair GM, Siciliano MJ, Brotherman KA, Nairn RS.
    Somat Cell Mol Genet; 1989 Jul; 15(4):271-7. PubMed ID: 2762931
    [Abstract] [Full Text] [Related]

  • 6. High-frequency mutation at the adenine phosphoribosyltransferase locus in Chinese hamster ovary cells due to deletion of the gene.
    Simon AE, Taylor MW.
    Proc Natl Acad Sci U S A; 1983 Feb; 80(3):810-4. PubMed ID: 6572371
    [Abstract] [Full Text] [Related]

  • 7. Mechanism of mutation at the aprt locus in Chinese hamster ovary cells: analysis of heterozygotes and hemizygotes.
    Simon AE, Taylor MW, Bradley WE.
    Mol Cell Biol; 1983 Oct; 3(10):1703-10. PubMed ID: 6646118
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

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  • 11. Allelic variation linked to adenine phosphoribosyltransferase locus in mouse teratocarcinoma cell line and feral-derived mouse strains.
    Turker MS, Stambrook PJ, Tischfield JA, Smith AC, Martin GM.
    Somat Cell Mol Genet; 1989 Mar; 15(2):159-66. PubMed ID: 2928841
    [Abstract] [Full Text] [Related]

  • 12. Targeted homologous recombination at the endogenous adenine phosphoribosyltransferase locus in Chinese hamster cells.
    Adair GM, Nairn RS, Wilson JH, Seidman MM, Brotherman KA, MacKinnon C, Scheerer JB.
    Proc Natl Acad Sci U S A; 1989 Jun; 86(12):4574-8. PubMed ID: 2734308
    [Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. Cloning the complete human adenine phosphoribosyl transferase gene.
    Murray AM, Drobetsky E, Arrand JE.
    Gene; 1984 Nov; 31(1-3):233-40. PubMed ID: 6241170
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  • 16. Model involving gene inactivation in the generation of autosomal recessive mutants in mammalian cells in culture.
    Simon AE, Taylor MW, Bradley WE, Thompson LH.
    Mol Cell Biol; 1982 Sep; 2(9):1126-33. PubMed ID: 6891022
    [Abstract] [Full Text] [Related]

  • 17. Sph I restriction fragment length polymorphism on human chromosome 16 detected with an APRT gene probe.
    Arrand JE, Murray AM, Spurr N.
    Nucleic Acids Res; 1987 Nov 25; 15(22):9615. PubMed ID: 2891115
    [No Abstract] [Full Text] [Related]

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  • 19. Reduction to homozygosity is the predominant spontaneous mutational event in cultured human lymphoblastoid cells.
    Klinedinst DK, Drinkwater NR.
    Mutat Res; 1991 Nov 25; 250(1-2):365-74. PubMed ID: 1682803
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