BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

295 related articles for article (PubMed ID: 15220921)

  • 1. A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A.
    Giglia-Mari G; Coin F; Ranish JA; Hoogstraten D; Theil A; Wijgers N; Jaspers NG; Raams A; Argentini M; van der Spek PJ; Botta E; Stefanini M; Egly JM; Aebersold R; Hoeijmakers JH; Vermeulen W
    Nat Genet; 2004 Jul; 36(7):714-9. PubMed ID: 15220921
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of TFB5, a new component of general transcription and DNA repair factor IIH.
    Ranish JA; Hahn S; Lu Y; Yi EC; Li XJ; Eng J; Aebersold R
    Nat Genet; 2004 Jul; 36(7):707-13. PubMed ID: 15220919
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Trichothiodystrophy view from the molecular basis of DNA repair/transcription factor TFIIH.
    Hashimoto S; Egly JM
    Hum Mol Genet; 2009 Oct; 18(R2):R224-30. PubMed ID: 19808800
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sublimiting concentration of TFIIH transcription/DNA repair factor causes TTD-A trichothiodystrophy disorder.
    Vermeulen W; Bergmann E; Auriol J; Rademakers S; Frit P; Appeldoorn E; Hoeijmakers JH; Egly JM
    Nat Genet; 2000 Nov; 26(3):307-13. PubMed ID: 11062469
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Splitting hairs--discovery of a new DNA repair and transcription factor for the human disease trichothiodystrophy.
    Cleaver JE
    DNA Repair (Amst); 2005 Feb; 4(2):285-7. PubMed ID: 15590337
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cloning and characterization of p52, the fifth subunit of the core of the transcription/DNA repair factor TFIIH.
    Marinoni JC; Roy R; Vermeulen W; Miniou P; Lutz Y; Weeda G; Seroz T; Gomez DM; Hoeijmakers JH; Egly JM
    EMBO J; 1997 Mar; 16(5):1093-102. PubMed ID: 9118947
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 18(5):1357-66. PubMed ID: 10064601
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 7(12):1990-8. PubMed ID: 18817897
    [TBL] [Abstract][Full Text] [Related]  

  • 9. p8/TTD-A as a repair-specific TFIIH subunit.
    Coin F; Proietti De Santis L; Nardo T; Zlobinskaya O; Stefanini M; Egly JM
    Mol Cell; 2006 Jan; 21(2):215-26. PubMed ID: 16427011
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Defective transcription/repair factor IIH recruitment to specific UV lesions in trichothiodystrophy syndrome.
    Chiganças V; Lima-Bessa KM; Stary A; Menck CF; Sarasin A
    Cancer Res; 2008 Aug; 68(15):6074-83. PubMed ID: 18676829
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy.
    Weeda G; Eveno E; Donker I; Vermeulen W; Chevallier-Lagente O; Taïeb A; Stary A; Hoeijmakers JH; Mezzina M; Sarasin A
    Am J Hum Genet; 1997 Feb; 60(2):320-9. PubMed ID: 9012405
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A history of TFIIH: two decades of molecular biology on a pivotal transcription/repair factor.
    Egly JM; Coin F
    DNA Repair (Amst); 2011 Jul; 10(7):714-21. PubMed ID: 21592869
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Solution structure and self-association properties of the p8 TFIIH subunit responsible for trichothiodystrophy.
    Vitorino M; Coin F; Zlobinskaya O; Atkinson RA; Moras D; Egly JM; Poterszman A; Kieffer B
    J Mol Biol; 2007 Apr; 368(2):473-80. PubMed ID: 17350038
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genotype-phenotype relationships in trichothiodystrophy patients with novel splicing mutations in the XPD gene.
    Botta E; Nardo T; Orioli D; Guglielmino R; Ricotti R; Bondanza S; Benedicenti F; Zambruno G; Stefanini M
    Hum Mutat; 2009 Mar; 30(3):438-45. PubMed ID: 19085937
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Trichothiodystrophy: from basic mechanisms to clinical implications.
    Stefanini M; Botta E; Lanzafame M; Orioli D
    DNA Repair (Amst); 2010 Jan; 9(1):2-10. PubMed ID: 19931493
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations in XPD helicase prevent its interaction and regulation by p44, another subunit of TFIIH, resulting in Xeroderma pigmentosum (XP) and trichothiodystrophy (TTD) phenotypes.
    Coin F; Marinoni JC; Egly JM
    Pathol Biol (Paris); 1998 Nov; 46(9):679-80. PubMed ID: 9885814
    [No Abstract]   [Full Text] [Related]  

  • 18. TFIIH contains a PH domain involved in DNA nucleotide excision repair.
    Gervais V; Lamour V; Jawhari A; Frindel F; Wasielewski E; Dubaele S; Egly JM; Thierry JC; Kieffer B; Poterszman A
    Nat Struct Mol Biol; 2004 Jul; 11(7):616-22. PubMed ID: 15195146
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hot news: temperature-sensitive humans explain hereditary disease.
    Friedberg EC
    Bioessays; 2001 Aug; 23(8):671-3. PubMed ID: 11494313
    [TBL] [Abstract][Full Text] [Related]  

  • 20. TTDA: big impact of a small protein.
    Theil AF; Hoeijmakers JH; Vermeulen W
    Exp Cell Res; 2014 Nov; 329(1):61-8. PubMed ID: 25016283
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.