128 related articles for article (PubMed ID: 17350038)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. Distinct roles for the XPB/p52 and XPD/p44 subcomplexes of TFIIH in damaged DNA opening during nucleotide excision repair.
Coin F; Oksenych V; Egly JM
Mol Cell; 2007 Apr; 26(2):245-56. PubMed ID: 17466626
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Small molecule-based targeting of TTD-A dimerization to control TFIIH transcriptional activity represents a potential strategy for anticancer therapy.
Gervais V; Muller I; Mari PO; Mourcet A; Movellan KT; Ramos P; Marcoux J; Guillet V; Javaid S; Burlet-Schiltz O; Czaplicki G; Milon A; Giglia-Mari G
J Biol Chem; 2018 Sep; 293(39):14974-14988. PubMed ID: 30068551
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Nucleotide excision repair/transcription gene defects in the fetus and impaired TFIIH-mediated function in transcription in placenta leading to preeclampsia.
Moslehi R; Ambroggio X; Nagarajan V; Kumar A; Dzutsev A
BMC Genomics; 2014 May; 15():373. PubMed ID: 24885447
[TBL] [Abstract][Full Text] [Related]
14. Reduced level of the repair/transcription factor TFIIH in trichothiodystrophy.
Botta E; Nardo T; Lehmann AR; Egly JM; Pedrini AM; Stefanini M
Hum Mol Genet; 2002 Nov; 11(23):2919-28. PubMed ID: 12393803
[TBL] [Abstract][Full Text] [Related]
15. Neurological defects in trichothiodystrophy reveal a coactivator function of TFIIH.
Compe E; Malerba M; Soler L; Marescaux J; Borrelli E; Egly JM
Nat Neurosci; 2007 Nov; 10(11):1414-22. PubMed ID: 17952069
[TBL] [Abstract][Full Text] [Related]
16. Characterization of a TFIIH homologue from Trypanosoma brucei.
Lecordier L; Devaux S; Uzureau P; Dierick JF; Walgraffe D; Poelvoorde P; Pays E; Vanhamme L
Mol Microbiol; 2007 Jun; 64(5):1164-81. PubMed ID: 17542913
[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. Domain architecture of the p62 subunit from the human transcription/repair factor TFIIH deduced by limited proteolysis and mass spectrometry analysis.
Jawhari A; Boussert S; Lamour V; Atkinson RA; Kieffer B; Poch O; Potier N; van Dorsselaer A; Moras D; Poterszman A
Biochemistry; 2004 Nov; 43(45):14420-30. PubMed ID: 15533047
[TBL] [Abstract][Full Text] [Related]
19. The cryo-electron microscopy structure of human transcription factor IIH.
Greber BJ; Nguyen THD; Fang J; Afonine PV; Adams PD; Nogales E
Nature; 2017 Sep; 549(7672):414-417. PubMed ID: 28902838
[TBL] [Abstract][Full Text] [Related]
20. The bZIP region of the plant transcription factor opaque-2 forms stable homodimers in solution and retains its helical structure upon subunit dissociation.
Moreau VH; da Silva AC; Siloto RM; Valente AP; Leite A; Almeida FC
Biochemistry; 2004 Apr; 43(16):4862-8. PubMed ID: 15096055
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
