Linkage between Werner Syndrome Protein and the Mre11 Complex via Nbs1
Open Access
- 1 May 2004
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 279 (20) , 21169-21176
- https://doi.org/10.1074/jbc.m312770200
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- Bloom syndrome cells undergo p53-dependent apoptosis and delayed assembly of BRCA1 and NBS1 repair complexes at stalled replication forksThe Journal of cell biology, 2003
- ATM-related Tel1 associates with double-strand breaks through an Xrs2-dependent mechanismGenes & Development, 2003
- Interaction of FANCD2 and NBS1 in the DNA damage responseNature Cell Biology, 2002
- Nbs1 is essential for DNA repair by homologous recombination in higher vertebrate cellsNature, 2002
- NBS1 Localizes to γ-H2AX Foci through Interaction with the FHA/BRCT DomainCurrent Biology, 2002
- Werner Protein Is a Target of DNA-dependent Protein Kinase in Vivo and in Vitro, and Its Catalytic Activities Are Regulated by PhosphorylationJournal of Biological Chemistry, 2002
- A Murine Model of Nijmegen Breakage SyndromeCurrent Biology, 2002
- Bloom's syndrome protein is required for correct relocalization of RAD50/MRE11/NBS1 complex after replication fork arrestThe Journal of cell biology, 2002
- Loss of Werner syndrome protein function promotes aberrant mitotic recombinationGenes & Development, 2001
- Werner syndrome cells are sensitive to DNA cross‐linking drugsThe FASEB Journal, 2001