BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

264 related articles for article (PubMed ID: 26149386)

  • 1. 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; 35(18):3178-88. PubMed ID: 26149386
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 26(2):231-43. PubMed ID: 17466625
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 11(12):942-50. PubMed ID: 23083890
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 133(7):1841-9. PubMed ID: 23370536
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 7(2):339-44. PubMed ID: 18077223
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 101(2):159-71. PubMed ID: 10786832
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Recognition of RNA polymerase II and transcription bubbles by XPG, CSB, and TFIIH: insights for transcription-coupled repair and Cockayne Syndrome.
    Sarker AH; Tsutakawa SE; Kostek S; Ng C; Shin DS; Peris M; Campeau E; Tainer JA; Nogales E; Cooper PK
    Mol Cell; 2005 Oct; 20(2):187-98. PubMed ID: 16246722
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Interactions involving the human RNA polymerase II transcription/nucleotide excision repair complex TFIIH, the nucleotide excision repair protein XPG, and Cockayne syndrome group B (CSB) protein.
    Iyer N; Reagan MS; Wu KJ; Canagarajah B; Friedberg EC
    Biochemistry; 1996 Feb; 35(7):2157-67. PubMed ID: 8652557
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Suppression of UV-induced apoptosis by the human DNA repair protein XPG.
    Clément V; Dunand-Sauthier I; Clarkson SG
    Cell Death Differ; 2006 Mar; 13(3):478-88. PubMed ID: 16167068
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 24(24):10670-80. PubMed ID: 15572672
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 34(3):481-9. PubMed ID: 23255472
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 117(25):14127-14138. PubMed ID: 32522879
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 243(1):22-8. PubMed ID: 9716445
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 12(4):389-96. PubMed ID: 15650764
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 17(7):e0271246. PubMed ID: 35802638
    [TBL] [Abstract][Full Text] [Related]  

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

  • 17. 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; 94(7):3116-21. PubMed ID: 9096355
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 275(5302):990-3. PubMed ID: 9020084
    [TBL] [Abstract][Full Text] [Related]  

  • 19. New insights into the combined Cockayne/xeroderma pigmentosum complex: human XPG protein can function in transcription factor stability.
    Friedberg EC; Wood RD
    Mol Cell; 2007 Apr; 26(2):162-4. PubMed ID: 17466619
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The founding members of xeroderma pigmentosum group G produce XPG protein with severely impaired endonuclease activity.
    Lalle P; Nouspikel T; Constantinou A; Thorel F; Clarkson SG
    J Invest Dermatol; 2002 Feb; 118(2):344-51. PubMed ID: 11841555
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.