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TFIIH: a key component in multiple DNA transactions.
Hoeijmakers JH, Egly JM, Vermeulen W. Hoeijmakers JH, et al. Among authors: vermeulen w. Curr Opin Genet Dev. 1996 Feb;6(1):26-33. doi: 10.1016/s0959-437x(96)90006-4. Curr Opin Genet Dev. 1996. PMID: 8791490 Review.
The DNA-dependent ATPase activity associated with the class II basic transcription factor BTF2/TFIIH.
Roy R, Schaeffer L, Humbert S, Vermeulen W, Weeda G, Egly JM. Roy R, et al. Among authors: vermeulen w. J Biol Chem. 1994 Apr 1;269(13):9826-32. J Biol Chem. 1994. PMID: 7511595
., and Reinberg, D. (1992) Nature 358, 641-645; Serizawa, H., Conaway, R. C., and Conaway, J. W. (1992) Proc. Natl. Acad. Sci. U.S.A. 89, 7476-7480; Feaver, W. ...We report here that a DNA-dependent ATPase and the previously characterized helicase (Schaeffer, L., Ro …
., and Reinberg, D. (1992) Nature 358, 641-645; Serizawa, H., Conaway, R. C., and Conaway, J. W. (1992) Proc. Natl. Acad. Sci. U.S.A. …
Nucleotide excision repair syndromes: molecular basis and clinical symptoms.
Bootsma D, Weeda G, Vermeulen W, van Vuuren H, Troelstra C, van der Spek P, Hoeijmakers J. Bootsma D, et al. Among authors: vermeulen w. Philos Trans R Soc Lond B Biol Sci. 1995 Jan 30;347(1319):75-81. doi: 10.1098/rstb.1995.0012. Philos Trans R Soc Lond B Biol Sci. 1995. PMID: 7746858 Review.
Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndrome.
Broughton BC, Thompson AF, Harcourt SA, Vermeulen W, Hoeijmakers JH, Botta E, Stefanini M, King MD, Weber CA, Cole J, et al. Broughton BC, et al. Among authors: vermeulen w. Am J Hum Genet. 1995 Jan;56(1):167-74. Am J Hum Genet. 1995. PMID: 7825573 Free PMC article. Review.
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