211 related articles for article (PubMed ID: 25431422)
1. A Drosophila XPD model links cell cycle coordination with neuro-development and suggests links to cancer.
Stettler K; Li X; Sandrock B; Braga-Lagache S; Heller M; Dümbgen L; Suter B
Dis Model Mech; 2015 Jan; 8(1):81-91. PubMed ID: 25431422
[TBL] [Abstract][Full Text] [Related]
2. XPB and XPD helicases in TFIIH orchestrate DNA duplex opening and damage verification to coordinate repair with transcription and cell cycle via CAK kinase.
Fuss JO; Tainer JA
DNA Repair (Amst); 2011 Jul; 10(7):697-713. PubMed ID: 21571596
[TBL] [Abstract][Full Text] [Related]
3. Abnormal XPD-induced nuclear receptor transactivation in DNA repair disorders: trichothiodystrophy and xeroderma pigmentosum.
Zhou X; Khan SG; Tamura D; Ueda T; Boyle J; Compe E; Egly JM; DiGiovanna JJ; Kraemer KH
Eur J Hum Genet; 2013 Aug; 21(8):831-7. PubMed ID: 23232694
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Functional and molecular genetic analyses of nine newly identified XPD-deficient patients reveal a novel mutation resulting in TTD as well as in XP/CS complex phenotypes.
Schäfer A; Gratchev A; Seebode C; Hofmann L; Schubert S; Laspe P; Apel A; Ohlenbusch A; Tzvetkov M; Weishaupt C; Oji V; Schön MP; Emmert S
Exp Dermatol; 2013 Jul; 22(7):486-9. PubMed ID: 23800062
[TBL] [Abstract][Full Text] [Related]
7. Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene.
Broughton BC; Berneburg M; Fawcett H; Taylor EM; Arlett CF; Nardo T; Stefanini M; Menefee E; Price VH; Queille S; Sarasin A; Bohnert E; Krutmann J; Davidson R; Kraemer KH; Lehmann AR
Hum Mol Genet; 2001 Oct; 10(22):2539-47. PubMed ID: 11709541
[TBL] [Abstract][Full Text] [Related]
8. Phenotype-specific adverse effects of XPD mutations on human prenatal development implicate impairment of TFIIH-mediated functions in placenta.
Moslehi R; Kumar A; Mills JL; Ambroggio X; Signore C; Dzutsev A
Eur J Hum Genet; 2012 Jun; 20(6):626-31. PubMed ID: 22234153
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Drosophila Xpd regulates Cdk7 localization, mitotic kinase activity, spindle dynamics, and chromosome segregation.
Li X; Urwyler O; Suter B
PLoS Genet; 2010 Mar; 6(3):e1000876. PubMed ID: 20300654
[TBL] [Abstract][Full Text] [Related]
11. Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene.
Taylor EM; Broughton BC; Botta E; Stefanini M; Sarasin A; Jaspers NG; Fawcett H; Harcourt SA; Arlett CF; Lehmann AR
Proc Natl Acad Sci U S A; 1997 Aug; 94(16):8658-63. PubMed ID: 9238033
[TBL] [Abstract][Full Text] [Related]
12. 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]
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. Effects of compound heterozygosity at the Xpd locus on cancer and ageing in mouse models.
van de Ven M; Andressoo JO; van der Horst GT; Hoeijmakers JH; Mitchell JR
DNA Repair (Amst); 2012 Nov; 11(11):874-83. PubMed ID: 23046824
[TBL] [Abstract][Full Text] [Related]
15. 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]
16.
Zurita M; Murillo-Maldonado JM
Int J Mol Sci; 2020 Jan; 21(2):. PubMed ID: 31963603
[TBL] [Abstract][Full Text] [Related]
17. Both XPD alleles contribute to the phenotype of compound heterozygote xeroderma pigmentosum patients.
Ueda T; Compe E; Catez P; Kraemer KH; Egly JM
J Exp Med; 2009 Dec; 206(13):3031-46. PubMed ID: 19934020
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. A yeast four-hybrid system identifies Cdk-activating kinase as a regulator of the XPD helicase, a subunit of transcription factor IIH.
Sandrock B; Egly JM
J Biol Chem; 2001 Sep; 276(38):35328-33. PubMed ID: 11445587
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]