194 related articles for article (PubMed ID: 9631660)
1. Dual functions of DNA repair genes: molecular, cellular, and clinical implications.
Lehmann AR
Bioessays; 1998 Feb; 20(2):146-55. PubMed ID: 9631660
[TBL] [Abstract][Full Text] [Related]
2. Mouse model for the DNA repair/basal transcription disorder trichothiodystrophy reveals cancer predisposition.
de Boer J; van Steeg H; Berg RJ; Garssen J; de Wit J; van Oostrum CT; Beems RB; van der Horst GT; van Kreijl CF; de Gruijl FR; Bootsma D; Hoeijmakers JH; Weeda G
Cancer Res; 1999 Jul; 59(14):3489-94. PubMed ID: 10416615
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Transcription by RNA polymerase II: a process linked to DNA repair.
Chalut C; Moncollin V; Egly JM
Bioessays; 1994 Sep; 16(9):651-5. PubMed ID: 7980491
[TBL] [Abstract][Full Text] [Related]
6. [Trichothiodystrophies: anomalies of the repair and transcription of genes].
Robert C; Sarasin A
Ann Dermatol Venereol; 1999 Oct; 126(10):669-71. PubMed ID: 10604001
[No Abstract] [Full Text] [Related]
7. 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]
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. Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy.
Broughton BC; Steingrimsdottir H; Weber CA; Lehmann AR
Nat Genet; 1994 Jun; 7(2):189-94. PubMed ID: 7920640
[TBL] [Abstract][Full Text] [Related]
10. A temperature-sensitive disorder in basal transcription and DNA repair in humans.
Vermeulen W; Rademakers S; Jaspers NG; Appeldoorn E; Raams A; Klein B; Kleijer WJ; Hansen LK; Hoeijmakers JH
Nat Genet; 2001 Mar; 27(3):299-303. PubMed ID: 11242112
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Interactions of the transcription/DNA repair factor TFIIH and XP repair proteins with DNA lesions in a cell-free repair assay.
Li RY; Calsou P; Jones CJ; Salles B
J Mol Biol; 1998 Aug; 281(2):211-8. PubMed ID: 9698541
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. The 14th Datta Lecture. TFIIH: from transcription to clinic.
Egly JM
FEBS Lett; 2001 Jun; 498(2-3):124-8. PubMed ID: 11412842
[TBL] [Abstract][Full Text] [Related]
18. Human nucleotide excision repair syndromes: molecular clues to unexpected intricacies.
Hoeijmakers JH
Eur J Cancer; 1994; 30A(13):1912-21. PubMed ID: 7734202
[No Abstract] [Full Text] [Related]
19. Xeroderma pigmentosum genes: functions inside and outside DNA repair.
Sugasawa K
Carcinogenesis; 2008 Mar; 29(3):455-65. PubMed ID: 18174245
[TBL] [Abstract][Full Text] [Related]
20. Strong functional interactions of TFIIH with XPC and XPG in human DNA nucleotide excision repair, without a preassembled repairosome.
Araújo SJ; Nigg EA; Wood RD
Mol Cell Biol; 2001 Apr; 21(7):2281-91. PubMed ID: 11259578
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]