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Mini-Review |
Assembly of multiprotein complexes that control genome function
Correspondence to Roel van Driel: r.vandriel{at}uva.nl
Live-cell imaging studies aided by mathematical modeling have provided unprecedented insight into assembly mechanisms of multiprotein complexes that control genome function. Such studies have unveiled emerging properties of chromatin-associated systems involved in DNA repair and transcription.
© 2009 Dinant et al.
This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jcb.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
C. Dinant's present address is Centre for Genotoxic Stress Research, Institute of Cancer Biology, Danish Cancer Society, DK-2100 Copenhagen, Denmark.
M.S. Luijsterburg's present address is Department of Cell and Molecular Biology, Karolinska Institute, S-17177 Stockholm, Sweden.
Abbreviations used in this paper: DSB, double strand break; HR, homologous recombination; NER, nucleotide excision repair; rRNA, ribosomal RNA; TFII, transcription factor II; XP, xeroderma pigmentosum protein.
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