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Journal Abstract Search

238 related items for PubMed ID: 9096355

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  • 3. Complementation of transformed fibroblasts from patients with combined xeroderma pigmentosum-Cockayne syndrome.
    Ellison AR, Nouspikel T, Jaspers NG, Clarkson SG, Gruenert DC.
    Exp Cell Res; 1998 Aug 25; 243(1):22-8. PubMed ID: 9716445
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  • 4. 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 25; 34(3):481-9. PubMed ID: 23255472
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  • 6. Human XPG nuclease structure, assembly, and activities with insights for neurodegeneration and cancer from pathogenic mutations.
    Tsutakawa SE, Sarker AH, Ng C, Arvai AS, Shin DS, Shih B, Jiang S, Thwin AC, Tsai MS, Willcox A, Her MZ, Trego KS, Raetz AG, Rosenberg D, Bacolla A, Hammel M, Griffith JD, Cooper PK, Tainer JA.
    Proc Natl Acad Sci U S A; 2020 Jun 23; 117(25):14127-14138. PubMed ID: 32522879
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  • 7. Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G.
    Cooper PK, Nouspikel T, Clarkson SG, Leadon SA.
    Science; 1997 Feb 14; 275(5302):990-3. PubMed ID: 9020084
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  • 8. 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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  • 9. 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 27; 69(2):291-300. PubMed ID: 11443545
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  • 10. Definition of a short region of XPG necessary for TFIIH interaction and stable recruitment to sites of UV damage.
    Thorel F, Constantinou A, Dunand-Sauthier I, Nouspikel T, Lalle P, Raams A, Jaspers NG, Vermeulen W, Shivji MK, Wood RD, Clarkson SG.
    Mol Cell Biol; 2004 Dec 27; 24(24):10670-80. PubMed ID: 15572672
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  • 11. Suppression of UV-induced apoptosis by the human DNA repair protein XPG.
    Clément V, Dunand-Sauthier I, Clarkson SG.
    Cell Death Differ; 2006 Mar 27; 13(3):478-88. PubMed ID: 16167068
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  • 12. Relationship of neurologic degeneration to genotype in three xeroderma pigmentosum group G patients.
    Emmert S, Slor H, Busch DB, Batko S, Albert RB, Coleman D, Khan SG, Abu-Libdeh B, DiGiovanna JJ, Cunningham BB, Lee MM, Crollick J, Inui H, Ueda T, Hedayati M, Grossman L, Shahlavi T, Cleaver JE, Kraemer KH.
    J Invest Dermatol; 2002 Jun 27; 118(6):972-82. PubMed ID: 12060391
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  • 13. Identification of the XPG region that causes the onset of Cockayne syndrome by using Xpg mutant mice generated by the cDNA-mediated knock-in method.
    Shiomi N, Kito S, Oyama M, Matsunaga T, Harada YN, Ikawa M, Okabe M, Shiomi T.
    Mol Cell Biol; 2004 May 27; 24(9):3712-9. PubMed ID: 15082767
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  • 14. Regulation of Transcription Elongation by the XPG-TFIIH Complex Is Implicated in Cockayne Syndrome.
    Narita T, Narita K, Takedachi A, Saijo M, Tanaka K.
    Mol Cell Biol; 2015 Sep 27; 35(18):3178-88. PubMed ID: 26149386
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  • 15. Xeroderma pigmentosum complementation group G associated with Cockayne syndrome.
    Vermeulen W, Jaeken J, Jaspers NG, Bootsma D, Hoeijmakers JH.
    Am J Hum Genet; 1993 Jul 27; 53(1):185-92. PubMed ID: 8317483
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  • 16. 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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  • 17. A stable XPG protein is required for proper ribosome biogenesis: Insights on the phenotype of combinate Xeroderma Pigmentosum/Cockayne Syndrome patients.
    Taupelet F, Donnio LM, Magnani C, Mari PO, Giglia-Mari G.
    PLoS One; 2022 Dec 01; 17(7):e0271246. PubMed ID: 35802638
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  • 18. 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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  • 19. Postnatal growth failure, short life span, and early onset of cellular senescence and subsequent immortalization in mice lacking the xeroderma pigmentosum group G gene.
    Harada YN, Shiomi N, Koike M, Ikawa M, Okabe M, Hirota S, Kitamura Y, Kitagawa M, Matsunaga T, Nikaido O, Shiomi T.
    Mol Cell Biol; 1999 Mar 14; 19(3):2366-72. PubMed ID: 10022922
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  • 20. Xeroderma pigmentosum and molecular cloning of DNA repair genes.
    Boulikas T.
    Anticancer Res; 1996 Mar 14; 16(2):693-708. PubMed ID: 8687116
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