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repair pol patient polymerase figure protein draq 5 synthesis replication mutation transcription mobility analysis ttd mice mouse pol effect lehmann damage tfiih dna repair level fi broblasts trichothiodystrophy incidence rad 18 c 7orf factor repair synthesis defect ner repair synthesis ubiquitination subunit result chromatin xeroderma pigmentosum xeroderma cell dna polymerases nucleus number pigmentosum stefanini ubiquitinated pcna uorescence vermeulen sirna pol 3 syndrome disorder fl uorescence pcna ubiquitination allele replication foci treatment interaction region phase kannouche depletion structure figure 1 deletion feature recruitment study ttd patients egfp-pol excision egfp-pol binding localization group lesion dna synthesis country table ubiquitinated broblast genet intercalation
10 Most Recent Publications
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SMC6 is an essential gene in mice, but a hypomorphic mutant in the ATPase domain has a mild phenotype with a range of subtle abnormalities
(Article)
Ju, L. Wing, J. Adler, T. Becker, J. Rozman, J. Klingenspor, M. Hanssen-de Wolf, J.E. Zimmer, A. Klopstock, T. Busch, D.H. Gailus-Durner, V. Fuchs, H. Taylor, M.E. Angelis, M.H. de Horst, G.T.J. van der Lehmann, A.R. Brandt, R.M.C. Slijepcevic, P. Horsch, M. Rathkolb, B. Rácz, I. Becker, M.L. Bijlsma, J.W.J. |
2013-03-19
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Influence of the live cell DNA marker DRAQ5 on chromatin-associated processes
(Article)
Mari, P.O. Verbiest, V. Sabbioneda, S. Gourdin, A.M. Wijgers, N. Dinant, C. Lehmann, A.R. Vermeulen, W. Giglia-Mari, G. |
2010-07-01
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Three DNA Polymerases, Recruited by Different Mechanisms, Carry Out NER Repair Synthesis in Human Cells
(Article)
Ogi, T. Limsirichaikul, S. Mullenders, L.H.F. Yamashita, S. Fousteri, M.I. Lehmann, A.R. Overmeer, R.M. Volker, M. Takenaka, K. Cloney, R. Nakazawa, Y. Niimi, A. Miki, Y. Jaspers, N.G.J. |
2010-03-12
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Effect of proliferating cell nuclear antigen ubiquitination and chromatin structure on the dynamic properties of the Y-family DNA polymerases
(Article)
Sabbioneda, S. Gourdin, A.M. Green, C.M. Zotter, A.M. Giglia-Mari, G. Houtsmuller, A.B. Vermeulen, W. Lehmann, A.R. |
2008-12-01
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Incidence of DNA repair deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy
(Article)
Kleijer, W.J. Laugel, V. Berneburg, M. Nardo, T. Fawcett, H. Gratchev, A. Jaspers, N.G.J. Sarasin, A. Stefanini, M. Lehmann, A.R. |
2008-05-03
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Mutations in the C7orf11 (TTDN1) gene in six nonphotosensitive trichothiodystrophy patients: No obvious genotype-phenotype relationships
(Article)
Botta, E. Offman, J. Sarasin, A. Lehmann, A.R. Stefanini, M. Nardo, T. Ricotti, R. Zambruno, G. Sansone, D. Balestri, P. Raams, A. Kleijer, W.J. Jaspers, N.G.J. |
2007-01-01
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A mouse model for the basal transcription/DNA repair disorder trichothiodystrophy.
(Article)
Boer, J. de Wit, J. de Steeg, H. van Berg, R.J.W. Morreau, H. Visser, P. Lehmann, A.R. Duran, M. Hoeijmakers, J.H.J. Weeda, G. |
1998-01-01
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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.
(Article)
Moriwaki, S-I. Stefanini, M. Kraemer, K.H. Lehmann, A.R. Hoeijmakers, J.H.J. Robbins, J.H. Rapin, I. Botta, E. Tanganelli, B. Vermeulen, W. Broughton, B.C. |
1996-01-01
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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 Cockayne syndrome.
(Article)
Broughton, B.C. Thompson, A.F. Arlett, C.F. Lehmann, A.R. Harcourt, S.A. Vermeulen, W. Hoeijmakers, J.H.J. Botta, E. Stefanini, M. King, M.D. Weber, C.A. Cole, J. |
1995-01-01
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Correction by the ERCC2 gene of UV sensitivity and repair deficiency phenotype in a subset of trichothiodystrophy cells.
(Article)
Mezzina, M. Eveno, E. Sarasin, A. Chevalier-Lagente, O. Benoit, A. Carreau, M. Vermeulen, W. Hoeijmakers, J.H.J. Stefanini, M. Lehmann, A.R. Weber, C.A. |
1994-01-01
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