| 1 | ERCC3, GTF2H1, KAT2A
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| Functional interplay between TFIIH and KAT2A regulates higher-order chromatin structure and class II gene expression.
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| Sandoz J, Nagy Z, Catez P, Caliskan G, Geny S, Renaud JB, Concordet JP, Poterszman A, Tora L, Egly JM, Le May N, Coin F.
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| Nat Commun 10(1):1288. doi: 10.1038/s41467-019-09270-2.
2019
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| 2 | ERCC2, ERCC3, GTF2H5, TTDA, TTDP, TTDP2, XPB, XPD
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| TFIIH Subunit Alterations Causing Xeroderma Pigmentosum and Trichothiodystrophy Specifically Disturb Several Steps during Transcription.
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| Singh A, Compe E, Le May N, Egly JM.
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| Am J Hum Genet 96(2):194-207. doi: 10.1016/j.ajhg.2014.12.012. Epub 2015 Jan 22.
2015
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| 3 | ERCC3
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| Structure of the C-terminal half of human XPB helicase and the impact of the disease-causing mutation XP11BE.
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| Hilario E, Li Y, Nobumori Y, Liu X, Fan L.
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| Acta Crystallogr D Biol Crystallogr 69(Pt 2):237-46. doi: 10.1107/S0907444912045040. Epub 2013 Jan 19.
2013
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| 4 | ERCC3
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| Deficiency in nucleotide excision repair family gene activity, especially ERCC3, is associated with non-pigmented hair fiber growth.
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| Yu M, Bell RH, Ho MM, Leung G, Haegert A, Carr N, Shapiro J, McElwee KJ.
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| PLoS One 7(5):e34185. doi: 10.1371/journal.pone.0034185. Epub 2012 May 16.
2012
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| 5 | ERCC2, ERCC3
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| The phosphorylation of the androgen receptor by TFIIH directs the ubiquitin/proteasome process.
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| Chymkowitch P, Le May N, Charneau P, Compe E, Egly JM.
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| EMBO J 30(3):468-79. doi: 10.1038/emboj.2010.337. Epub 2010 Dec 14.
2011
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| 6 | C1D, ERCC3
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| XPB induces C1D expression to counteract UV-induced apoptosis.
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| Li G, Liu J, Abu-Asab M, Masabumi S, Maru Y.
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| Mol Cancer Res 8(6):885-95. doi: 10.1158/1541-7786.MCR-09-0467. Epub 2010 Jun 8. 2010
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| 7 | ERCC3, TUBG1
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| The TFIIH subunit p89 (XPB) localizes to the centrosome during mitosis.
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| Weber A, Chung HJ, Springer E, Heitzmann D, Warth R.
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| Cell Oncol 32(1-2):121-30. doi: 10.3233/CLO-2009-0509.
2010
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| 8 | ERCC2, ERCC3
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| Molecular insights into the recruitment of TFIIH to sites of DNA damage.
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| Oksenych V, de Jesus BB, Zhovmer A, Egly JM, Coin F.
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| EMBO J 28(19):2971-80. Epub 2009 Aug 27.
2009
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| 9 | CHUK, ERCC3, IKBKG
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| Association between genetic variants in VEGF, ERCC3 and occupational benzene haematotoxicity.
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| Hosgood HD 3rd, Zhang L, Shen M, Berndt SI, Vermeulen R, Li G, Yin S, Yeager M, Yuenger J, Rothman N, Chanock S, Smith M, Lan Q.
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| Occup Environ Med 66(12):848-53. Epub 2009 Sep 22. 2009
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| 10 | ERCC3
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| Influence of XPB helicase on recruitment and redistribution of nucleotide excision repair proteins at sites of UV-induced DNA damage.
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| Oh KS, Imoto K, Boyle J, Khan SG, Kraemer KH.
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| DNA Repair (Amst) 6(9):1359-70. Epub 2007 May 16.
2007
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| 11 | ERCC3, GTF2H4
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| Distinct roles for the XPB/p52 and XPD/p44 subcomplexes of TFIIH in damaged DNA opening during nucleotide excision repair.
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| Coin F, Oksenych V, Egly JM.
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| Mol Cell 26(2):245-56. 2007
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| 12 | COPS2, ERCC3, TRIP11
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| Detection and identification of transcription factors as interaction partners of alien in vivo.
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| Kob R, Baniahmad A, Escher N, von Eggeling F, Melle C.
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| Cell Cycle 6(8):993-6. Epub 2007 Apr 7.PMID: 17438371 2007
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| 13 | ERCC3, XPB
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| Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome.
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| Oh KS, Khan SG, Jaspers NG, Raams A, Ueda T, Lehmann A, Friedmann PS, Emmert S, Gratchev A, Lachlan K, Lucassan A, Baker CC, Kraemer KH.
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| Hum Mutat 27(11):1092-103. 2006
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| 14 | DDB1, DDB2, ERCC2, ERCC3, ERCC4, ERCC5, XPA, XPC
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| Clusters of transcription-coupled repair in the human genome.
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| Surralles J, Ramirez MJ, Marcos R, Natarajan AT, Mullenders LH.
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| Proc Natl Acad Sci U S A 99(16):10571-4. 2002
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| 15 | ERCC1, ERCC3, ERCC5, ERCC6
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| Expression of nucleotide excision repair genes and the risk for squamous cell carcinoma of the head and neck.
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| Cheng L, Sturgis EM, Eicher SA, Spitz MR, Wei Q.
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| Cancer 94(2):393-7. 2002
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| 16 | ERCC3, TTDA, XPB
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| Sublimiting concentration of TFIIH transcription/DNA repair factor causes TTD-A trichothiodystrophy disorder.
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| Vermeulen W, Bergmann E, Auriol J, Rademakers S, Frit P, Appeldoorn E, Hoeijmakers JH, Egly JM.
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| Nat Genet 26(3):307-13. 2000
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| 17 | ERCC3
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| Mechanism of ATP-dependent promoter melting by transcription factor IIH.
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| Kim TK, Ebright RH, Reinberg D.
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| Science 288(5470):1418-22. 2000
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| 18 | ERCC2, ERCC3
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| Mutations in XPB and XPD helicases found in xeroderma pigmentosum patients impair the transcription function of TFIIH.
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| Coin F, et al.
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| EMBO J 18(5):1357-1366. 1999
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| 19 | ERCC3, XPB
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| A mutation in repB, the dictyostelium homolog of the human xeroderma pigmentosum B gene, has increased sensitivity to UV-light but normal morphogenesis.
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| Lee SK, et al.
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| Biochim Biophys Acta 1399 : 161-172. 1998
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| 20 | ERCC3, XPB
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| A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy.
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| Weeda G, et al.
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| Am J Hum Genet 60 : 320-329. 1997
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| 21 | ERCC3, XPB
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| A 3'-5' XPB helicase defect in repair/transcription factor TFIIH of xeroderma pigmentosum group B affects both DNA repair and transcription.
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| Hwang JR, et al.
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| J Biol Chem 271 : 15898-15904. 1996
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| 22 | ERCC2, ERCC3
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| Reconstitution of TFIIH and requirement of its DNA helicase subunits, Rad3 and Rad25, in the incision step of nucleotide excision repair.
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| Sung P, et al.
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| J Biol Chem 271 : 10821-10826. 1996
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| 23 | XPB, ERCC3
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| Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3.
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| Vermeulen W, et al.
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| Am J Hum Genet 54 : 191-200. 1994
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| 24 | ERCC3, XPB
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| Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH).
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| Van Vuuren AJ, et al.
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| EMBO J 13 : 1645-1653. 1994
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| 25 | ERCC3
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| RAD25 is a DNA helicase required for DNA repair and RNA polymerase II transcription.
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| Guzder SN, et al.
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| Nature 369 : 578-581. 1994
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| 26 | ERCC3
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| DNA repair helicase : a component of BTF2 (TFIIH) basic transcription factor.
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| Schaeffer L, et al.
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| Science 260 : 58-63. 1993
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| 27 | ERCC3
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| Molecular and functional analysis of the XPBC/ERCC-3 promoter : transcription activity is dependent on the integrity of an Sp1-binding site.
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| Ma L, et al.
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| Nucleic Acids Res 20 : 217-224. 1992
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| 28 | ERCC3, XPB
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| A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome.
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| Weeda G, et al.
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| Cell 62 : 777-791. 1990
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| 29 | ERCC3
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| Molecular cloning and biological characterization of the human excision repair gene ERCC-3.
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| Weeda G, van Ham RC, Masurel R, Westerveld A, Odijk H, de Wit J, Bootsma D, van der Eb AJ, Hoeijmakers JH.
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| Mol Cell Biol 10(6):2570-81. 1990
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| 30 | CD3EAP, ERCC3, ERCC6
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| (Sub)chromosomal localization of the human excision repair genes ERCC-3 and -6, and identification of a gene (ASE-1) overlapping with ERCC-1.
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| Hoeijmakers JHJ, et al.
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| (HGM10) Cytogenet Cell Genet 51 : 1014. 1989
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| 31 | ERCC3, ERCC5
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| Identification of nucleotide-excision-repair genes on human chromosomes 2 and 13 by functional complementation in hamster-human hybrids.
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| Thompson LH, Carrano AV, Sato K, Salazar EP, White BF, Stewart SA, Minkler JL, Siciliano MJ.
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| Somat Cell Mol Genet 13 : 539-551. 1987
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| 32 | ERCC3, ERCC4, ERCC5, XRCC1
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| Chromosomal assignments of human DNA repair genes that complement chinese hamster ovary (CHO) cell mutants.
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| Siciliano MJ, et al.
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| (HGM9) Cytogenet Cell Genet 46 : 691. 1987
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| 33 | ERCC3, ERCC4
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| Assignment of a human DNA repair gene associated with sister-chromatid exchange to chromosome 19.
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| Siciliano MJ, et al.
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| Mutat Res 174 : 303-308. 1986
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| 34 | ERCC3
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| 31.
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| Telomere attrition and genomic instability in xeroderma pigmentosum type-b deficient fibroblasts under oxidative stress.
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| Ting AP, Low GK, Gopalakrishnan K, Hande MP ing AP, Low GK, Gopalakrishnan K, Hande MP.
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