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Journal Abstract Search

320 related items for PubMed ID: 9765592

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  • 3. Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome.
    Oh KS, Khan SG, Jaspers NG, Raams A, Ueda T, Lehmann A, Friedmann PS, Emmert S, Gratchev A, Lachlan K, Lucassan A, Baker CC, Kraemer KH.
    Hum Mutat; 2006 Nov; 27(11):1092-103. PubMed ID: 16947863
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  • 6. Differential developmental expression of the rep B and rep D xeroderma pigmentosum related DNA helicase genes from Dictyostelium discoideum.
    Lee SK, Yu SL, Garcia MX, Alexander H, Alexander S.
    Nucleic Acids Res; 1997 Jun 15; 25(12):2365-74. PubMed ID: 9171087
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  • 7. 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
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  • 8. Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy.
    Graham JM, Anyane-Yeboa K, Raams A, Appeldoorn E, Kleijer WJ, Garritsen VH, Busch D, Edersheim TG, Jaspers NG.
    Am J Hum Genet; 2001 Aug 01; 69(2):291-300. PubMed ID: 11443545
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  • 10. Common pathways for ultraviolet skin carcinogenesis in the repair and replication defective groups of xeroderma pigmentosum.
    Cleaver JE.
    J Dermatol Sci; 2000 May 01; 23(1):1-11. PubMed ID: 10699759
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  • 12. Lack of CAK complex accumulation at DNA damage sites in XP-B and XP-B/CS fibroblasts reveals differential regulation of CAK anchoring to core TFIIH by XPB and XPD helicases during nucleotide excision repair.
    Zhu Q, Wani G, Sharma N, Wani A.
    DNA Repair (Amst); 2012 Dec 01; 11(12):942-50. PubMed ID: 23083890
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  • 14. 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
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  • 15. Influence of XPB helicase on recruitment and redistribution of nucleotide excision repair proteins at sites of UV-induced DNA damage.
    Oh KS, Imoto K, Boyle J, Khan SG, Kraemer KH.
    DNA Repair (Amst); 2007 Sep 01; 6(9):1359-70. PubMed ID: 17509950
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  • 16. A 3' --> 5' XPB helicase defect in repair/transcription factor TFIIH of xeroderma pigmentosum group B affects both DNA repair and transcription.
    Hwang JR, Moncollin V, Vermeulen W, Seroz T, van Vuuren H, Hoeijmakers JH, Egly JM.
    J Biol Chem; 1996 Jul 05; 271(27):15898-904. PubMed ID: 8663148
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  • 17. Transcriptional profiles of unirradiated or UV-irradiated human cells expressing either the cancer-prone XPB/CS allele or the noncancer-prone XPB/TTD allele.
    da Costa RM, Riou L, Paquola A, Menck CF, Sarasin A.
    Oncogene; 2005 Feb 17; 24(8):1359-74. PubMed ID: 15608684
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  • 19. 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
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  • 20. The 14th Datta Lecture. TFIIH: from transcription to clinic.
    Egly JM.
    FEBS Lett; 2001 Jun 08; 498(2-3):124-8. PubMed ID: 11412842
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