239 related articles for article (PubMed ID: 8194528)
1. The ERCC2/DNA repair protein is associated with the class II BTF2/TFIIH transcription factor.
Schaeffer L; Moncollin V; Roy R; Staub A; Mezzina M; Sarasin A; Weeda G; Hoeijmakers JH; Egly JM
EMBO J; 1994 May; 13(10):2388-92. PubMed ID: 8194528
[TBL] [Abstract][Full Text] [Related]
2. Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH).
van Vuuren AJ; Vermeulen W; Ma L; Weeda G; Appeldoorn E; Jaspers NG; van der Eb AJ; Bootsma D; Hoeijmakers JH; Humbert S
EMBO J; 1994 Apr; 13(7):1645-53. PubMed ID: 8157004
[TBL] [Abstract][Full Text] [Related]
3. Dual role of TFIIH in DNA excision repair and in transcription by RNA polymerase II.
Drapkin R; Reardon JT; Ansari A; Huang JC; Zawel L; Ahn K; Sancar A; Reinberg D
Nature; 1994 Apr; 368(6473):769-72. PubMed ID: 8152490
[TBL] [Abstract][Full Text] [Related]
4. Isolation and characterization of two human transcription factor IIH (TFIIH)-related complexes: ERCC2/CAK and TFIIH.
Reardon JT; Ge H; Gibbs E; Sancar A; Hurwitz J; Pan ZQ
Proc Natl Acad Sci U S A; 1996 Jun; 93(13):6482-7. PubMed ID: 8692841
[TBL] [Abstract][Full Text] [Related]
5. DNA repair helicase: a component of BTF2 (TFIIH) basic transcription factor.
Schaeffer L; Roy R; Humbert S; Moncollin V; Vermeulen W; Hoeijmakers JH; Chambon P; Egly JM
Science; 1993 Apr; 260(5104):58-63. PubMed ID: 8465201
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. p44 and p34 subunits of the BTF2/TFIIH transcription factor have homologies with SSL1, a yeast protein involved in DNA repair.
Humbert S; van Vuuren H; Lutz Y; Hoeijmakers JH; Egly JM; Moncollin V
EMBO J; 1994 May; 13(10):2393-8. PubMed ID: 8194529
[TBL] [Abstract][Full Text] [Related]
8. Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH.
Coin F; Marinoni JC; Rodolfo C; Fribourg S; Pedrini AM; Egly JM
Nat Genet; 1998 Oct; 20(2):184-8. PubMed ID: 9771713
[TBL] [Abstract][Full Text] [Related]
9. TFIIH: a link between transcription, DNA repair and cell cycle regulation.
Seroz T; Hwang JR; Moncollin V; Egly JM
Curr Opin Genet Dev; 1995 Apr; 5(2):217-21. PubMed ID: 7613092
[TBL] [Abstract][Full Text] [Related]
10. Persistence of repair proteins at unrepaired DNA damage distinguishes diseases with ERCC2 (XPD) mutations: cancer-prone xeroderma pigmentosum vs. non-cancer-prone trichothiodystrophy.
Boyle J; Ueda T; Oh KS; Imoto K; Tamura D; Jagdeo J; Khan SG; Nadem C; Digiovanna JJ; Kraemer KH
Hum Mutat; 2008 Oct; 29(10):1194-208. PubMed ID: 18470933
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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; 271(27):15898-904. PubMed ID: 8663148
[TBL] [Abstract][Full Text] [Related]
13. GTF2E2 Mutations Destabilize the General Transcription Factor Complex TFIIE in Individuals with DNA Repair-Proficient Trichothiodystrophy.
Kuschal C; Botta E; Orioli D; Digiovanna JJ; Seneca S; Keymolen K; Tamura D; Heller E; Khan SG; Caligiuri G; Lanzafame M; Nardo T; Ricotti R; Peverali FA; Stephens R; Zhao Y; Lehmann AR; Baranello L; Levens D; Kraemer KH; Stefanini M
Am J Hum Genet; 2016 Apr; 98(4):627-42. PubMed ID: 26996949
[TBL] [Abstract][Full Text] [Related]
14. TFIIH subunit alterations causing xeroderma pigmentosum and trichothiodystrophy specifically disturb several steps during transcription.
Singh A; Compe E; Le May N; Egly JM
Am J Hum Genet; 2015 Feb; 96(2):194-207. PubMed ID: 25620205
[TBL] [Abstract][Full Text] [Related]
15. 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; 273(43):27794-9. PubMed ID: 9774388
[TBL] [Abstract][Full Text] [Related]
16. Cloning of a human homolog of the yeast nucleotide excision repair gene MMS19 and interaction with transcription repair factor TFIIH via the XPB and XPD helicases.
Seroz T; Winkler GS; Auriol J; Verhage RA; Vermeulen W; Smit B; Brouwer J; Eker AP; Weeda G; Egly JM; Hoeijmakers JH
Nucleic Acids Res; 2000 Nov; 28(22):4506-13. PubMed ID: 11071939
[TBL] [Abstract][Full Text] [Related]
17. Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3.
Vermeulen W; Scott RJ; Rodgers S; Müller HJ; Cole J; Arlett CF; Kleijer WJ; Bootsma D; Hoeijmakers JH; Weeda G
Am J Hum Genet; 1994 Feb; 54(2):191-200. PubMed ID: 8304337
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Functional interactions between p53 and the TFIIH complex are affected by tumour-associated mutations.
Léveillard T; Andera L; Bissonnette N; Schaeffer L; Bracco L; Egly JM; Wasylyk B
EMBO J; 1996 Apr; 15(7):1615-24. PubMed ID: 8612585
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]