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444 related items for PubMed ID: 9426063

  • 1. Disruption of the mouse xeroderma pigmentosum group D DNA repair/basal transcription gene results in preimplantation lethality.
    de Boer J, Donker I, de Wit J, Hoeijmakers JH, Weeda G.
    Cancer Res; 1998 Jan 01; 58(1):89-94. PubMed ID: 9426063
    [Abstract] [Full Text] [Related]

  • 2. Mouse model for the DNA repair/basal transcription disorder trichothiodystrophy reveals cancer predisposition.
    de Boer J, van Steeg H, Berg RJ, Garssen J, de Wit J, van Oostrum CT, Beems RB, van der Horst GT, van Kreijl CF, de Gruijl FR, Bootsma D, Hoeijmakers JH, Weeda G.
    Cancer Res; 1999 Jul 15; 59(14):3489-94. PubMed ID: 10416615
    [Abstract] [Full Text] [Related]

  • 3. Mutations in the XPD gene in xeroderma pigmentosum group D cell strains: confirmation of genotype-phenotype correlation.
    Kobayashi T, Uchiyama M, Fukuro S, Tanaka K.
    Am J Med Genet; 2002 Jul 01; 110(3):248-52. PubMed ID: 12116233
    [Abstract] [Full Text] [Related]

  • 4. Mutations in the XPD gene leading to xeroderma pigmentosum symptoms.
    Kobayashi T, Kuraoka I, Saijo M, Nakatsu Y, Tanaka A, Someda Y, Fukuro S, Tanaka K.
    Hum Mutat; 1997 Jul 01; 9(4):322-31. PubMed ID: 9101292
    [Abstract] [Full Text] [Related]

  • 5. Defects in the DNA repair and transcription gene ERCC2 in the cancer-prone disorder xeroderma pigmentosum group D.
    Takayama K, Salazar EP, Lehmann A, Stefanini M, Thompson LH, Weber CA.
    Cancer Res; 1995 Dec 01; 55(23):5656-63. PubMed ID: 7585650
    [Abstract] [Full Text] [Related]

  • 6. Human xeroderma pigmentosum group D gene encodes a DNA helicase.
    Sung P, Bailly V, Weber C, Thompson LH, Prakash L, Prakash S.
    Nature; 1993 Oct 28; 365(6449):852-5. PubMed ID: 8413672
    [Abstract] [Full Text] [Related]

  • 7. Restoring DNA repair capacity of cells from three distinct diseases by XPD gene-recombinant adenovirus.
    Armelini MG, Muotri AR, Marchetto MC, de Lima-Bessa KM, Sarasin A, Menck CF.
    Cancer Gene Ther; 2005 Apr 28; 12(4):389-96. PubMed ID: 15650764
    [Abstract] [Full Text] [Related]

  • 8. Comparative study of nucleotide excision repair defects between XPD-mutated fibroblasts derived from trichothiodystrophy and xeroderma pigmentosum patients.
    Nishiwaki T, Kobayashi N, Iwamoto T, Yamamoto A, Sugiura S, Liu YC, Sarasin A, Okahashi Y, Hirano M, Ueno S, Mori T.
    DNA Repair (Amst); 2008 Dec 01; 7(12):1990-8. PubMed ID: 18817897
    [Abstract] [Full Text] [Related]

  • 9. A temperature-sensitive disorder in basal transcription and DNA repair in humans.
    Vermeulen W, Rademakers S, Jaspers NG, Appeldoorn E, Raams A, Klein B, Kleijer WJ, Hansen LK, Hoeijmakers JH.
    Nat Genet; 2001 Mar 01; 27(3):299-303. PubMed ID: 11242112
    [Abstract] [Full Text] [Related]

  • 10. Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy.
    Broughton BC, Steingrimsdottir H, Weber CA, Lehmann AR.
    Nat Genet; 1994 Jun 01; 7(2):189-94. PubMed ID: 7920640
    [Abstract] [Full Text] [Related]

  • 11. Xeroderma pigmentosum and molecular cloning of DNA repair genes.
    Boulikas T.
    Anticancer Res; 1996 Jun 01; 16(2):693-708. PubMed ID: 8687116
    [Abstract] [Full Text] [Related]

  • 12. Mutations in XPB and XPD helicases found in xeroderma pigmentosum patients impair the transcription function of TFIIH.
    Coin F, Bergmann E, Tremeau-Bravard A, Egly JM.
    EMBO J; 1999 Mar 01; 18(5):1357-66. PubMed ID: 10064601
    [Abstract] [Full Text] [Related]

  • 13. The cancer-free phenotype in trichothiodystrophy is unrelated to its repair defect.
    Berneburg M, Clingen PH, Harcourt SA, Lowe JE, Taylor EM, Green MH, Krutmann J, Arlett CF, Lehmann AR.
    Cancer Res; 2000 Jan 15; 60(2):431-8. PubMed ID: 10667598
    [Abstract] [Full Text] [Related]

  • 14. Trichothiodystrophy: update on the sulfur-deficient brittle hair syndromes.
    Itin PH, Sarasin A, Pittelkow MR.
    J Am Acad Dermatol; 2001 Jun 15; 44(6):891-920; quiz 921-4. PubMed ID: 11369901
    [Abstract] [Full Text] [Related]

  • 15. Recovery of normal DNA repair and mutagenesis in trichothiodystrophy cells after transduction of the XPD human gene.
    Marionnet C, Quilliet X, Benoit A, Armier J, Sarasin A, Stary A.
    Cancer Res; 1996 Dec 01; 56(23):5450-6. PubMed ID: 8968100
    [Abstract] [Full Text] [Related]

  • 16. Drug-induced apoptosis is delayed and reduced in XPD lymphoblastoid cell lines: possible role of TFIIH in p53-mediated apoptotic cell death.
    Robles AI, Wang XW, Harris CC.
    Oncogene; 1999 Aug 19; 18(33):4681-8. PubMed ID: 10467415
    [Abstract] [Full Text] [Related]

  • 17. DNA repair characteristics and mutations in the ERCC2 DNA repair and transcription gene in a trichothiodystrophy patient.
    Takayama K, Danks DM, Salazar EP, Cleaver JE, Weber CA.
    Hum Mutat; 1997 Aug 19; 9(6):519-25. PubMed ID: 9195225
    [Abstract] [Full Text] [Related]

  • 18. Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene.
    Broughton BC, Berneburg M, Fawcett H, Taylor EM, Arlett CF, Nardo T, Stefanini M, Menefee E, Price VH, Queille S, Sarasin A, Bohnert E, Krutmann J, Davidson R, Kraemer KH, Lehmann AR.
    Hum Mol Genet; 2001 Oct 15; 10(22):2539-47. PubMed ID: 11709541
    [Abstract] [Full Text] [Related]

  • 19. Association of the DNA repair gene XPD Asp312Asn polymorphism with p53 gene mutations in tobacco-related non-small cell lung cancer.
    Gao WM, Romkes M, Day RD, Siegfried JM, Luketich JD, Mady HH, Melhem MF, Keohavong P.
    Carcinogenesis; 2003 Oct 15; 24(10):1671-6. PubMed ID: 12844488
    [Abstract] [Full Text] [Related]

  • 20. Mechanism of open complex and dual incision formation by human nucleotide excision repair factors.
    Evans E, Moggs JG, Hwang JR, Egly JM, Wood RD.
    EMBO J; 1997 Nov 03; 16(21):6559-73. PubMed ID: 9351836
    [Abstract] [Full Text] [Related]

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