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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

147 related items for PubMed ID: 2011791

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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 01; 26(21):4888-94. PubMed ID: 9776749
    [Abstract] [Full Text] [Related]

  • 8. 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 Nov 01; 28(4):471-82. PubMed ID: 8991080
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Assignment of the gene for adenine phosphoribosyltransferase on the genetic map of mouse chromosome 8.
    Nesterova TB, Borodin PM, Zakian SM, Serov OL.
    Biochem Genet; 1987 Aug 01; 25(7-8):563-8. PubMed ID: 3447590
    [Abstract] [Full Text] [Related]

  • 13. 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 03; 96(16):9230-5. PubMed ID: 10430925
    [Abstract] [Full Text] [Related]

  • 14. 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 03; 3(10):1703-10. PubMed ID: 6646118
    [Abstract] [Full Text] [Related]

  • 15. 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 03; 80(3):810-4. PubMed ID: 6572371
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No 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 03; 16(3):225-30. PubMed ID: 1972816
    [Abstract] [Full Text] [Related]

  • 18. Selection of human cells having two different types of mutations in individual cells (genetic/artificial mutants). Application to the diagnosis of the heterozygous state for a type of adenine phosphoribosyltransferase deficiency.
    Kamatani N, Kuroshima S, Terai C, Kawai K, Mikanagi K, Nishioka K.
    Hum Genet; 1987 Jun 03; 76(2):148-52. PubMed ID: 3610146
    [Abstract] [Full Text] [Related]

  • 19. [Adenine phosphoribosyltransferase(APRT) deficiency].
    Kamatani N.
    Nihon Rinsho; 1996 Dec 03; 54(12):3321-7. PubMed ID: 8976113
    [Abstract] [Full Text] [Related]

  • 20. Identification of a compound heterozygote for adenine phosphoribosyltransferase deficiency (APRT*J/APART*Q0) leading to 2,8-dihydroxyadenine urolithiasis.
    Kamatani N, Kuroshima S, Yamanaka H, Nakashe S, Take H, Hakoda M.
    Hum Genet; 1990 Oct 03; 85(5):500-4. PubMed ID: 2227934
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.