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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

145 related articles for article (PubMed ID: 1381471)

  • 21. Similarity of in vivo somatic mutations at an autosomal adenine phosphoribosyltransferase locus between T- and B-cells in human peripheral blood.
    Hakoda M; Kamatani N; Terai C; Yamanaka H; Taniguchi A; Ueda H; Kashiwazaki S
    Mutat Res; 1996 Oct; 357(1-2):107-13. PubMed ID: 8876686
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The aprt heterozygote/hemizygote system for screening mutagenic agents allows detection of large deletions.
    Bradley WE; Belouchi A; Messing K
    Mutat Res; 1988 May; 199(1):131-8. PubMed ID: 3362154
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A mutant allele common to the type I adenine phosphoribosyltransferase deficiency in Japanese subjects.
    Mimori A; Hidaka Y; Wu VC; Tarlé SA; Kamatani N; Kelley WN; Pallela TD
    Am J Hum Genet; 1991 Jan; 48(1):103-7. PubMed ID: 1985452
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. 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]  

  • 27. 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]  

  • 28. 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]  

  • 29. End extension repair of introduced targeting vectors mediated by homologous recombination in mammalian cells.
    Aratani Y; Okazaki R; Koyama H
    Nucleic Acids Res; 1992 Sep; 20(18):4795-801. PubMed ID: 1408793
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Crossovers within a short DNA sequence indicate a long evolutionary history of the APRT*J mutation.
    Kamatani N; Kuroshima S; Hakoda M; Palella TD; Hidaka Y
    Hum Genet; 1990 Oct; 85(6):600-4. PubMed ID: 2227951
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mutagenicity testing in mammalian cells. I. Derivation of a Chinese hamster ovary cell line heterozygous for the adenine phosphoribosyltransferase and thymidine kinase loci.
    Adair GM; Carver JH; Wandres DL
    Mutat Res; 1980 Sep; 72(2):187-205. PubMed ID: 6449663
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Human adenine phosphoribosyltransferase deficiency. Demonstration of a single mutant allele common to the Japanese.
    Hidaka Y; Tarlé SA; Fujimori S; Kamatani N; Kelley WN; Palella TD
    J Clin Invest; 1988 Mar; 81(3):945-50. PubMed ID: 3343350
    [TBL] [Abstract][Full Text] [Related]  

  • 35. DNA sequence analysis of mutations induced by melphalan in the CHO aprt locus.
    Austin MJ; Han YH; Povirk LF
    Cancer Genet Cytogenet; 1992 Nov; 64(1):69-74. PubMed ID: 1458453
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. The mutational specificity of simulated sunlight at the aprt locus in rodent cells.
    Drobetsky EA; Moustacchi E; Glickman BW; Sage E
    Carcinogenesis; 1994 Aug; 15(8):1577-83. PubMed ID: 8055636
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Loss of heterozygosity and base substitution at the APRT locus in mismatch-repair-proficient and -deficient colorectal carcinoma cell lines.
    Phear G; Bhattacharyya NP; Meuth M
    Mol Cell Biol; 1996 Nov; 16(11):6516-23. PubMed ID: 8887680
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.