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Journal Abstract Search

468 related items for PubMed ID: 10786832

  • 1. Transcription-coupled repair of 8-oxoguanine: requirement for XPG, TFIIH, and CSB and implications for Cockayne syndrome.
    Le Page F, Kwoh EE, Avrutskaya A, Gentil A, Leadon SA, Sarasin A, Cooper PK.
    Cell; 2000 Apr 14; 101(2):159-71. PubMed ID: 10786832
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  • 2. 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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  • 9. XPG stabilizes TFIIH, allowing transactivation of nuclear receptors: implications for Cockayne syndrome in XP-G/CS patients.
    Ito S, Kuraoka I, Chymkowitch P, Compe E, Takedachi A, Ishigami C, Coin F, Egly JM, Tanaka K.
    Mol Cell; 2007 Apr 27; 26(2):231-43. PubMed ID: 17466625
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  • 14. RNA polymerase II elongation complexes containing the Cockayne syndrome group B protein interact with a molecular complex containing the transcription factor IIH components xeroderma pigmentosum B and p62.
    Tantin D.
    J Biol Chem; 1998 Oct 23; 273(43):27794-9. PubMed ID: 9774388
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  • 15. Novel XPG (ERCC5) mutations affect DNA repair and cell survival after ultraviolet but not oxidative stress.
    Soltys DT, Rocha CR, Lerner LK, de Souza TA, Munford V, Cabral F, Nardo T, Stefanini M, Sarasin A, Cabral-Neto JB, Menck CF.
    Hum Mutat; 2013 Mar 23; 34(3):481-9. PubMed ID: 23255472
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  • 17. Hot topics in DNA repair: the molecular basis for different disease states caused by mutations in TFIIH and XPG.
    Schärer OD.
    DNA Repair (Amst); 2008 Feb 01; 7(2):339-44. PubMed ID: 18077223
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  • 18. Characterization of three XPG-defective patients identifies three missense mutations that impair repair and transcription.
    Schäfer A, Schubert S, Gratchev A, Seebode C, Apel A, Laspe P, Hofmann L, Ohlenbusch A, Mori T, Kobayashi N, Schürer A, Schön MP, Emmert S.
    J Invest Dermatol; 2013 Jul 01; 133(7):1841-9. PubMed ID: 23370536
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  • 19. Reduced RNA polymerase II transcription in extracts of cockayne syndrome and xeroderma pigmentosum/Cockayne syndrome cells.
    Dianov GL, Houle JF, Iyer N, Bohr VA, Friedberg EC.
    Nucleic Acids Res; 1997 Sep 15; 25(18):3636-42. PubMed ID: 9278484
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  • 20. A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function.
    Nouspikel T, Lalle P, Leadon SA, Cooper PK, Clarkson SG.
    Proc Natl Acad Sci U S A; 1997 Apr 01; 94(7):3116-21. PubMed ID: 9096355
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