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

230 related items for PubMed ID: 9472693

  • 1. Complete restoration of normal DNA repair characteristics in group F xeroderma pigmentosum cells by over-expression of transfected XPF cDNA.
    Yagi T, Matsumura Y, Sato M, Nishigori C, Mori T, Sijbers AM, Takebe H.
    Carcinogenesis; 1998 Jan; 19(1):55-60. PubMed ID: 9472693
    [Abstract] [Full Text] [Related]

  • 2. Defining the function of xeroderma pigmentosum group F protein in psoralen interstrand cross-link-mediated DNA repair and mutagenesis.
    Chen Z, Xu XS, Harrison J, Wang G.
    Biochem J; 2004 Apr 01; 379(Pt 1):71-8. PubMed ID: 14728600
    [Abstract] [Full Text] [Related]

  • 3. Sensitivity of group F xeroderma pigmentosum cells to UV and mitomycin C relative to levels of XPF and ERCC1 overexpression.
    Yagi T, Katsuya A, Koyano A, Takebe H.
    Mutagenesis; 1998 Nov 01; 13(6):595-9. PubMed ID: 9862190
    [Abstract] [Full Text] [Related]

  • 4. Analysis of point mutations in an ultraviolet-irradiated shuttle vector plasmid propagated in cells from Japanese xeroderma pigmentosum patients in complementation groups A and F.
    Yagi T, Tatsumi-Miyajima J, Sato M, Kraemer KH, Takebe H.
    Cancer Res; 1991 Jun 15; 51(12):3177-82. PubMed ID: 2039995
    [Abstract] [Full Text] [Related]

  • 5. Expression of a transfected DNA repair gene (XPA) in xeroderma pigmentosum group A cells restores normal DNA repair and mutagenesis of UV-treated plasmids.
    Levy DD, Saijo M, Tanaka K, Kraemer KH.
    Carcinogenesis; 1995 Jul 15; 16(7):1557-63. PubMed ID: 7614689
    [Abstract] [Full Text] [Related]

  • 6. Stable transformation of xeroderma pigmentosum group A cells with an XPA minigene restores normal DNA repair and mutagenesis of UV-treated plasmids.
    Myrand SP, Topping RS, States JC.
    Carcinogenesis; 1996 Sep 15; 17(9):1909-17. PubMed ID: 8824513
    [Abstract] [Full Text] [Related]

  • 7. Characterization of molecular defects in xeroderma pigmentosum group F in relation to its clinically mild symptoms.
    Matsumura Y, Nishigori C, Yagi T, Imamura S, Takebe H.
    Hum Mol Genet; 1998 Jun 15; 7(6):969-74. PubMed ID: 9580660
    [Abstract] [Full Text] [Related]

  • 8. DNA repair and ultraviolet mutagenesis in cells from a new patient with xeroderma pigmentosum group G and cockayne syndrome resemble xeroderma pigmentosum cells.
    Moriwaki S, Stefanini M, Lehmann AR, Hoeijmakers JH, Robbins JH, Rapin I, Botta E, Tanganelli B, Vermeulen W, Broughton BC, Kraemer KH.
    J Invest Dermatol; 1996 Oct 15; 107(4):647-53. PubMed ID: 8823375
    [Abstract] [Full Text] [Related]

  • 9. Evidence for defective repair of cyclobutane pyrimidine dimers with normal repair of other DNA photoproducts in a transcriptionally active gene transfected into Cockayne syndrome cells.
    Barrett SF, Robbins JH, Tarone RE, Kraemer KH.
    Mutat Res; 1991 Nov 15; 255(3):281-91. PubMed ID: 1719400
    [Abstract] [Full Text] [Related]

  • 10. UV-induced mutations in a shuttle vector replicated in repair deficient trichothiodystrophy cells differ with those in genetically-related cancer prone xeroderma pigmentosum.
    Madzak C, Armier J, Stary A, Daya-Grosjean L, Sarasin A.
    Carcinogenesis; 1993 Jul 15; 14(7):1255-60. PubMed ID: 8392442
    [Abstract] [Full Text] [Related]

  • 11. Ultraviolet-induced mutations in Cockayne syndrome cells are primarily caused by cyclobutane dimer photoproducts while repair of other photoproducts is normal.
    Parris CN, Kraemer KH.
    Proc Natl Acad Sci U S A; 1993 Aug 01; 90(15):7260-4. PubMed ID: 8346243
    [Abstract] [Full Text] [Related]

  • 12. Xeroderma pigmentosum group F protein binds to Eg5 and is required for proper mitosis: implications for XP-F and XFE.
    Tan LJ, Saijo M, Kuraoka I, Narita T, Takahata C, Iwai S, Tanaka K.
    Genes Cells; 2012 Mar 01; 17(3):173-85. PubMed ID: 22353549
    [Abstract] [Full Text] [Related]

  • 13. Respective roles of cyclobutane pyrimidine dimers, (6-4)photoproducts, and minor photoproducts in ultraviolet mutagenesis of repair-deficient xeroderma pigmentosum A cells.
    Otoshi E, Yagi T, Mori T, Matsunaga T, Nikaido O, Kim ST, Hitomi K, Ikenaga M, Todo T.
    Cancer Res; 2000 Mar 15; 60(6):1729-35. PubMed ID: 10749146
    [Abstract] [Full Text] [Related]

  • 14. Expression of the cDNA for the beta subunit of human casein kinase II confers partial UV resistance on xeroderma pigmentosum cells.
    Teitz T, Eli D, Penner M, Bakhanashvili M, Naiman T, Timme TL, Wood CM, Moses RE, Canaani D.
    Mutat Res; 1990 Jul 15; 236(1):85-97. PubMed ID: 1694965
    [Abstract] [Full Text] [Related]

  • 15. Characteristics of UV-induced mutation spectra in human XP-D/ERCC2 gene-mutated xeroderma pigmentosum and trichothiodystrophy cells.
    Marionnet C, Benoit A, Benhamou S, Sarasin A, Stary A.
    J Mol Biol; 1995 Oct 06; 252(5):550-62. PubMed ID: 7563073
    [Abstract] [Full Text] [Related]

  • 16. Xeroderma pigmentosum variant cells are less likely than normal cells to incorporate dAMP opposite photoproducts during replication of UV-irradiated plasmids.
    Wang YC, Maher VM, McCormick JJ.
    Proc Natl Acad Sci U S A; 1991 Sep 01; 88(17):7810-4. PubMed ID: 1652764
    [Abstract] [Full Text] [Related]

  • 17. UV-induced base substitution mutations in a shuttle vector plasmid propagated in group C xeroderma pigmentosum cells.
    Yagi T, Sato M, Tatsumi-Miyajima J, Takebe H.
    Mutat Res; 1992 Mar 01; 273(2):213-20. PubMed ID: 1372104
    [Abstract] [Full Text] [Related]

  • 18. Ultraviolet hypermutability of a shuttle vector propagated in xeroderma pigmentosum variant cells.
    Waters HL, Seetharam S, Seidman MM, Kraemer KH.
    J Invest Dermatol; 1993 Nov 01; 101(5):744-8. PubMed ID: 8228338
    [Abstract] [Full Text] [Related]

  • 19. Repair of damaged DNA by extracts from a xeroderma pigmentosum complementation group A revertant and expression of a protein absent in its parental cell line.
    Jones CJ, Cleaver JE, Wood RD.
    Nucleic Acids Res; 1992 Mar 11; 20(5):991-5. PubMed ID: 1549511
    [Abstract] [Full Text] [Related]

  • 20. Mislocalization of XPF-ERCC1 nuclease contributes to reduced DNA repair in XP-F patients.
    Ahmad A, Enzlin JH, Bhagwat NR, Wijgers N, Raams A, Appledoorn E, Theil AF, J Hoeijmakers JH, Vermeulen W, J Jaspers NG, Schärer OD, Niedernhofer LJ.
    PLoS Genet; 2010 Mar 05; 6(3):e1000871. PubMed ID: 20221251
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 12.