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

632 related items for PubMed ID: 11710928

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

  • 2. 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]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 5. Persistence of repair proteins at unrepaired DNA damage distinguishes diseases with ERCC2 (XPD) mutations: cancer-prone xeroderma pigmentosum vs. non-cancer-prone trichothiodystrophy.
    Boyle J, Ueda T, Oh KS, Imoto K, Tamura D, Jagdeo J, Khan SG, Nadem C, Digiovanna JJ, Kraemer KH.
    Hum Mutat; 2008 Oct 15; 29(10):1194-208. PubMed ID: 18470933
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. 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 Oct 15; 9(4):322-31. PubMed ID: 9101292
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. 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]

  • 12. Analysis of mutations in the XPD gene in Italian patients with trichothiodystrophy: site of mutation correlates with repair deficiency, but gene dosage appears to determine clinical severity.
    Botta E, Nardo T, Broughton BC, Marinoni S, Lehmann AR, Stefanini M.
    Am J Hum Genet; 1998 Oct 01; 63(4):1036-48. PubMed ID: 9758621
    [Abstract] [Full Text] [Related]

  • 13. Different removal of ultraviolet photoproducts in genetically related xeroderma pigmentosum and trichothiodystrophy diseases.
    Eveno E, Bourre F, Quilliet X, Chevallier-Lagente O, Roza L, Eker AP, Kleijer WJ, Nikaido O, Stefanini M, Hoeijmakers JH.
    Cancer Res; 1995 Oct 01; 55(19):4325-32. PubMed ID: 7671243
    [Abstract] [Full Text] [Related]

  • 14. Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene.
    Taylor EM, Broughton BC, Botta E, Stefanini M, Sarasin A, Jaspers NG, Fawcett H, Harcourt SA, Arlett CF, Lehmann AR.
    Proc Natl Acad Sci U S A; 1997 Aug 05; 94(16):8658-63. PubMed ID: 9238033
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. 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 05; 12(4):389-96. PubMed ID: 15650764
    [Abstract] [Full Text] [Related]

  • 18. Trichothiodystrophy fibroblasts are deficient in the repair of ultraviolet-induced cyclobutane pyrimidine dimers and (6-4)photoproducts.
    Nishiwaki Y, Kobayashi N, Imoto K, Iwamoto TA, Yamamoto A, Katsumi S, Shirai T, Sugiura S, Nakamura Y, Sarasin A, Miyagawa S, Mori T.
    J Invest Dermatol; 2004 Feb 05; 122(2):526-32. PubMed ID: 15009740
    [Abstract] [Full Text] [Related]

  • 19. Photocarcinogenesis and inhibition of intercellular adhesion molecule 1 expression in cells of DNA-repair-defective individuals.
    Ahrens C, Grewe M, Berneburg M, Grether-Beck S, Quilliet X, Mezzina M, Sarasin A, Lehmann AR, Arlett CF, Krutmann J.
    Proc Natl Acad Sci U S A; 1997 Jun 24; 94(13):6837-41. PubMed ID: 9192652
    [Abstract] [Full Text] [Related]

  • 20. 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]

    Page: [Next] [New Search]
    of 32.