Novel Human and Mouse Homologs of Saccharomyces cerevisiae DNA Polymerase η von McDonald, John P., Rapić-Otrin, Vesna, Epstein, Jonathan A., Broughton, Bernard C., Wang, Xiangyuan, Lehmann, Alan R., Wolgemuth, Debra J., Woodgate, Roger

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Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene von BROUGHTON, Bernard C, BERNEBURG, Mark, SARASIN, Alain, BOHNERT, Elisabeth, KRUTMANN, Jean, DAVIDSON, Rosemarie, KRAEMER, Kenneth H, LEHMANN, Alan R, FAWCETT, Heather, TAYLOR, Elaine M, ARLETT, Colin F, NARDO, Tiziana, STEFANINI, Miria, MENEFEE, Emory, PRICE, Vera H, QUEILLE, Sophie

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Defects in the DNA repair and transcription gene ERCC2(XPD) in trichothiodystrophy von TAKAYAMA, K, SALAZAR, E. P, BROUGHTON, B. C, LEHMANN, A. R, SARASIN, A, THOMPSON, L. H, WEBER, C. A

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Domain structure, localization, and function of DNA polymerase eta, defective in xeroderma pigmentosum variant cells von Kannouche, P, Broughton, B C, Volker, M, Hanaoka, F, Mullenders, L H, Lehmann, A R

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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 co... von BROUGHTON, B. C, THOMPSON, A. F, ARLETT, C. F, LEHMANN, A. R, HARCOURT, S. A, VERMEULEN, W, HOEJIMAKERS, J. H. J, BOTTA, E, STEFANINI, M, KING, M. D, WEBER, C. A, COLE, J

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Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy von Broughton, Bernard C, Steingrimsdottir, Herdis, Weber, Christine A, Lehmann, Alan R

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Molecular Analysis of Mutations in DNA Polymerase η in Xeroderma Pigmentosum-Variant Patients von Broughton, Bernard C., Cordonnier, Agnes, Kleijer, Wim J., Nicolaas G. J. Jaspers, Fawcett, Heather, Raams, Anja, Garritsen, Victor H., Stary, Anne, Avril, Marie-Françoise, Boudsocq, François, Masutani, Chikahide, Hanaoka, Fumio, Fuchs, Robert P., Sarasin, Alain, Lehmann, Alan R.

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Xeroderma Pigmentosum and Trichothiodystrophy are Associated with Different Mutations in the XPD (ERCC2) Repair/Transcription Gene von Taylor, Elaine M., Broughton, Bernard C., Botta, Elena, Stefanini, Miria, Sarasin, Alain, Nicolaas G. J. Jaspers, Fawcett, Heather, Harcourt, Susan A., Arlett, Colin F., Lehmann, Alan R.

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Localization of a DNA Repair Gene (XRCC5) Involved in Double-Strand-Break Rejoining to Human Chromosome 2 von Jeggo, P. A., Hafezparast, M., Thompson, A. F., Broughton, B. C., Kaur, G. P., Zdzienicka, M. Z., Athwal, R. S.

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Mutations in the XPC gene in families with xeroderma pigmentosum and consequences at the cell, protein, and transcript levels von Chavanne, F, Broughton, B C, Pietra, D, Nardo, T, Browitt, A, Lehmann, A R, Stefanini, M

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Mutations in the general transcription factor TFIIH result in β-thalassaemia in individuals with trichothiodystrophy von VIPRAKASIT, Vip, GIBBONS, Richard J, LEHMANN, Alan R, HIGGS, Douglas R, BROUGHTON, Bernard C, TOLMIE, John L, BROWN, Donald, LUNT, Peter, WINTER, Robin M, MARINONI, Stefano, STEFANINI, Miria, BRUETON, Louise

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Analysis of Mutations in the XPD Gene in Italian Patients with Trichothiodystrophy: Site of Mutation Correlates with Repair Deficiency, but Gene Dosage Appears to Determine Clinica... von Botta, Elena, Nardo, Tiziana, Broughton, Bernard C., Marinoni, Stefano, Lehmann, Alan R., Stefanini, Miria

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Cloning the RAD51 homologue of Schizosaccharomyces pombe von Muris, D.F.R, Vreeken, K, Carr, A.M, Broughton, B.C, Lehmann, A.R, Lohmann, P.H.M, Pastink, A

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Cells from an Immunodeficient Patient (46BR) with a Defect in DNA Ligation are Hypomutable but Hypersensitive to the Induction of Sister Chromatid Exchanges von Henderson, Leigh M., Arlett, Colin F., Harcourt, Susan A., Lehmann, Alan R., Broughton, Bernard C.

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Trichothiodystrophy, a human DNA repair disorder with heterogeneity in the cellular response to ultraviolet light von LEHMANN, A. R, ARLETT, C. F, MACKIE, R. M, STEPHENSON, J. B. P, TOLMIE, J. L, BROUGHTON, B. C, HARCOURT, S. A, STEINGRIMSDOTTIR, H, STEFANINI, M, TAYLOR, A. M. R, NATARAJAN, A. T, GREEN, S, KING, M. D

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Relation between the human fibroblast strain 46BR and cell lines representative of Bloom's syndrome von LEHMANN, A. R, WILLIS, A. E, BROUGHTON, B. C, JAMES, M. R, STEINGRIMSDOTTIR, H, HARCOURT, S. A, ARLETT, C. F, LINDAHL, T

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Poly(ADP-ribosylation) reduces the steady-state level of breaks in DNA following treatment of human cells with alkylating agents von Lehmann, A.R., Broughton, B. C.

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Inhibition of DNA Replication by Ionizing Radiation is Mediated by a Trans-acting Factor von Lamb, J.R., Petit-Frère, C., Broughton, B.C., Lehmann, A.R., Green, M.H.L.

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DNA Repair and Ultraviolet Mutagenesis in Cells From a New Patient With Xeroderma Pigmentosum Group G and Cockayne Syndrome Resemble Xeroderma Pigmentosum Cells von Moriwaki, Shin-Ichi, Stafanim, Miria, Lehmann, Alan R., Hoeijmakers, Jan H.J., Robbins, Jay H., Rapin, Isablle, Botta, Elena, Tanganelli, Bianca, Vermeulen, Wim, Broughton, Benard C., Kraemer, Kenneth H.

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A biochemical defect in the repair of alkylated DNA in cells from an immunodeficient patient (46BR) von Teo, I.A., Broughton, B.C., Day, R.S., James, M.R., Karren, P., Mayne, L.V., Lehmann, A.R.

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