"Molecular cloning and biological characterization of the human excision repair gene ERCC-3."
Weeda G. , van Ham R.C.A. , Masurel R. , Westerveld A. , Odijk H. , de Wit J. , Bootsma D. , van der Eb A.J. , Hoeijmakers J.H.J.
Mol. Cell. Biol.10:2570-2581(1990) [PubMed] [Europe PMC] [Abstract]

"A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders Xeroderma pigmentosum and Cockayne's syndrome."
Weeda G. , van Ham R.C.A. , Vermeulen W. , Bootsma D. , van der Eb A.J. , Hoeijmakers J.H.J.
Cell62:777-791(1990) [PubMed] [Europe PMC] [Abstract]

"Structure and expression of the human XPBC/ERCC-3 gene involved in DNA repair disorders xeroderma pigmentosum and Cockayne's syndrome."
Weeda G. , Ma L. , van Ham R.C.A. , van der Eb A.J. , Hoeijmakers J.H.J.
Nucleic Acids Res.19:6301-6308(1991) [PubMed] [Europe PMC] [Abstract]

NIEHS SNPs program
Submitted (2002-10) to the EMBL/GenBank/DDBJ databases

"Generation and annotation of the DNA sequences of human chromosomes 2 and 4."
Hillier L.W. , Graves T.A. , Fulton R.S. , Fulton L.A. , Pepin K.H. , Minx P. , Wagner-McPherson C. , Layman D. , Wylie K. , Sekhon M. , Becker M.C. , Fewell G.A. , Delehaunty K.D. , Miner T.L. , Nash W.E. , Kremitzki C. , Oddy L. , Du H. , Sun H. , Bradshaw-Cordum H. , Ali J. , Carter J. , Cordes M. , Harris A. , Isak A. , van Brunt A. , Nguyen C. , Du F. , Courtney L. , Kalicki J. , Ozersky P. , Abbott S. , Armstrong J. , Belter E.A. , Caruso L. , Cedroni M. , Cotton M. , Davidson T. , Desai A. , Elliott G. , Erb T. , Fronick C. , Gaige T. , Haakenson W. , Haglund K. , Holmes A. , Harkins R. , Kim K. , Kruchowski S.S. , Strong C.M. , Grewal N. , Goyea E. , Hou S. , Levy A. , Martinka S. , Mead K. , McLellan M.D. , Meyer R. , Randall-Maher J. , Tomlinson C. , Dauphin-Kohlberg S. , Kozlowicz-Reilly A. , Shah N. , Swearengen-Shahid S. , Snider J. , Strong J.T. , Thompson J. , Yoakum M. , Leonard S. , Pearman C. , Trani L. , Radionenko M. , Waligorski J.E. , Wang C. , Rock S.M. , Tin-Wollam A.-M. , Maupin R. , Latreille P. , Wendl M.C. , Yang S.-P. , Pohl C. , Wallis J.W. , Spieth J. , Bieri T.A. , Berkowicz N. , Nelson J.O. , Osborne J. , Ding L. , Meyer R. , Sabo A. , Shotland Y. , Sinha P. , Wohldmann P.E. , Cook L.L. , Hickenbotham M.T. , Eldred J. , Williams D. , Jones T.A. , She X. , Ciccarelli F.D. , Izaurralde E. , Taylor J. , Schmutz J. , Myers R.M. , Cox D.R. , Huang X. , McPherson J.D. , Mardis E.R. , Clifton S.W. , Warren W.C. , Chinwalla A.T. , Eddy S.R. , Marra M.A. , Ovcharenko I. , Furey T.S. , Miller W. , Eichler E.E. , Bork P. , Suyama M. , Torrents D. , Waterston R.H. , Wilson R.K. more...
Nature434:724-731(2005) [PubMed] [Europe PMC] [Abstract]

Mural R.J. , Istrail S. , Sutton G.G. , Florea L. , Halpern A.L. , Mobarry C.M. , Lippert R. , Walenz B. , Shatkay H. , Dew I. , Miller J.R. , Flanigan M.J. , Edwards N.J. , Bolanos R. , Fasulo D. , Halldorsson B.V. , Hannenhalli S. , Turner R. , Yooseph S. , Lu F. , Nusskern D.R. , Shue B.C. , Zheng X.H. , Zhong F. , Delcher A.L. , Huson D.H. , Kravitz S.A. , Mouchard L. , Reinert K. , Remington K.A. , Clark A.G. , Waterman M.S. , Eichler E.E. , Adams M.D. , Hunkapiller M.W. , Myers E.W. , Venter J.C. more...
Submitted (2005-07) to the EMBL/GenBank/DDBJ databases

"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res.14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]

"Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH)."
van Vuuren A.J. , Vermeulen W. , Ma L. , Weeda G. , Appeldoorn E. , Jaspers N.G.J. , van der Eb A.J. , Bootsma D. , Hoeijmakers J.H.J. , Humbert S. , Schaeffer L. , Egly J.-M.
EMBO J.13:1645-1653(1994) [PubMed] [Europe PMC] [Abstract]

"The 62- and 80-kDa subunits of transcription factor IIH mediate the interaction with Epstein-Barr virus nuclear protein 2."
Tong X. , Drapkin R. , Reinberg D. , Kieff E.
Proc. Natl. Acad. Sci. U.S.A.92:3259-3263(1995) [PubMed] [Europe PMC] [Abstract]

"Immunoaffinity purification and functional characterization of human transcription factor IIH and RNA polymerase II from clonal cell lines that conditionally express epitope-tagged subunits of the multiprotein complexes."
Kershnar E. , Wu S.-Y. , Chiang C.-M.
J. Biol. Chem.273:34444-34453(1998) [PubMed] [Europe PMC] [Abstract]

"Reconstitution of the transcription factor TFIIH: assignment of functions for the three enzymatic subunits, XPB, XPD, and cdk7."
Tirode F. , Busso D. , Coin F. , Egly J.-M.
Mol. Cell3:87-95(1999) [PubMed] [Europe PMC] [Abstract]

"The FBP interacting repressor targets TFIIH to inhibit activated transcription."
Liu J. , He L. , Collins I. , Ge H. , Libutti D. , Li J. , Egly J.-M. , Levens D.
Mol. Cell5:331-341(2000) [PubMed] [Europe PMC] [Abstract]

"Defective interplay of activators and repressors with TFIH in xeroderma pigmentosum."
Liu J. , Akoulitchev S. , Weber A. , Ge H. , Chuikov S. , Libutti D. , Wang X.W. , Conaway J.W. , Harris C.C. , Conaway R.C. , Reinberg D. , Levens D.
Cell104:353-363(2001) [PubMed] [Europe PMC] [Abstract]

"A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy."
Cleaver J.E. , Thompson L.H. , Richardson A.S. , States J.C.
Hum. Mutat.14:9-22(1999) [PubMed] [Europe PMC] [Abstract]

"MCAF1/AM is involved in Sp1-mediated maintenance of cancer-associated telomerase activity."
Liu L. , Ishihara K. , Ichimura T. , Fujita N. , Hino S. , Tomita S. , Watanabe S. , Saitoh N. , Ito T. , Nakao M.
J. Biol. Chem.284:5165-5174(2009) [PubMed] [Europe PMC] [Abstract]

"Structure of the C-terminal half of human XPB helicase and the impact of the disease-causing mutation XP11BE."
Hilario E. , Li Y. , Nobumori Y. , Liu X. , Fan L.
Acta Crystallogr. D69:237-246(2013) [PubMed] [Europe PMC] [Abstract]

"Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3."
Vermeulen W. , Scott R.J. , Rodgers S. , Mueller H.J. , Cole J. , Arlett C.F. , Kleijer W.J. , Bootsma D. , Hoeijmakers J.H.J. , Weeda G.
Am. J. Hum. Genet.54:191-200(1994) [PubMed] [Europe PMC] [Abstract]

"A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy."
Weeda G. , Eveno E. , Donker I. , Vermeulen W. , Chevallier-Lagente O. , Taieb A. , Stary A. , Hoeijmakers J.H.J. , Mezzina M. , Sarasin A.
Am. J. Hum. Genet.60:320-329(1997) [PubMed] [Europe PMC] [Abstract]

"Identification of four single nucleotide polymorphisms in DNA repair genes: XPA and XPB (ERCC3) in Polish population."
Butkiewicz D. , Rusin M. , Harris C.C. , Chorazy M.
Hum. Mutat.15:577-578(2000) [PubMed] [Europe PMC] [Abstract]

"Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome."
Oh K.-S. , Khan S.G. , Jaspers N.G.J. , Raams A. , Ueda T. , Lehmann A. , Friedmann P.S. , Emmert S. , Gratchev A. , Lachlan K. , Lucassan A. , Baker C.C. , Kraemer K.H.
Hum. Mutat.27:1092-1103(2006) [PubMed] [Europe PMC] [Abstract]

"The consensus coding sequences of human breast and colorectal cancers."
Sjoeblom T. , Jones S. , Wood L.D. , Parsons D.W. , Lin J. , Barber T.D. , Mandelker D. , Leary R.J. , Ptak J. , Silliman N. , Szabo S. , Buckhaults P. , Farrell C. , Meeh P. , Markowitz S.D. , Willis J. , Dawson D. , Willson J.K.V. , Gazdar A.F. , Hartigan J. , Wu L. , Liu C. , Parmigiani G. , Park B.H. , Bachman K.E. , Papadopoulos N. , Vogelstein B. , Kinzler K.W. , Velculescu V.E. more...
Science314:268-274(2006) [PubMed] [Europe PMC] [Abstract]