BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

97 related articles for article (PubMed ID: 7660991)

  • 1. Germline and somatic mutation at the APRT locus of mice and man.
    Tischfield JA; Engle SJ; Gupta PK; Bye S; Boyadjiev S; Shao C; O'Neill P; Albertini RJ; Stambrook PJ; Sahota AS
    Adv Exp Med Biol; 1994; 370():661-4. PubMed ID: 7660991
    [No Abstract]   [Full Text] [Related]  

  • 2. Analysis of in vivo somatic mutations at the APRT locus.
    Gupta PK; Sahota A; Boyadjiev SA; Bye S; O'Neill JP; Hunter TC; Albertini RJ; Tischfield JA
    Adv Exp Med Biol; 1994; 370():653-6. PubMed ID: 7660989
    [No Abstract]   [Full Text] [Related]  

  • 3. Germline and somatic mutations leading to adenine phosphoribosyltransferase (APRT) deficiency.
    Hakoda M; Kamatani N; Ohtsuka S; Kashiwazaki S
    Adv Exp Med Biol; 1991; 309B():87-90. PubMed ID: 1781412
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Homozygous deficiency at autosomal locus aprt in human somatic cells in vivo induced by two different mechanisms.
    Hakoda M; Nishioka K; Kamatani N
    Cancer Res; 1990 Mar; 50(6):1738-41. PubMed ID: 2306728
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. A new location for the human adenine phosphoribosyltransferase gene (APRT) distal to the haptoglobin (HP) and fra(16)(q23)(FRA16D) loci.
    Fratini A; Simmers RN; Callen DF; Hyland VJ; Tischfield JA; Stambrook PJ; Sutherland GR
    Cytogenet Cell Genet; 1986; 43(1-2):10-3. PubMed ID: 3780312
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mitotic recombination produces the majority of recessive fibroblast variants in heterozygous mice.
    Shao C; Deng L; Henegariu O; Liang L; Raikwar N; Sahota A; Stambrook PJ; Tischfield JA
    Proc Natl Acad Sci U S A; 1999 Aug; 96(16):9230-5. PubMed ID: 10430925
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of polymorphic markers flanking the human APRT gene.
    Boyadjiev SA; Sahota A; Tischfield JA
    Adv Exp Med Biol; 1994; 370():657-60. PubMed ID: 7660990
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. High frequency in vivo loss of heterozygosity is primarily a consequence of mitotic recombination.
    Gupta PK; Sahota A; Boyadjiev SA; Bye S; Shao C; O'Neill JP; Hunter TC; Albertini RJ; Stambrook PJ; Tischfield JA
    Cancer Res; 1997 Mar; 57(6):1188-93. PubMed ID: 9067291
    [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. 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]  

  • 17. 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]  

  • 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. 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]  

  • 20. [Localization of the gene coding for adenine phosphoribosyltransferase on the genetic map of chromosome 8 in the mouse].
    Nesterova TB; Borodin PM; Zakiian SM
    Genetika; 1988 May; 24(5):829-35. PubMed ID: 3417135
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.