The Tandem BRCT Domain of 53BP1 Is Not Required for Its Repair Function
Open Access
- 1 December 2006
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 281 (50) , 38472-38477
- https://doi.org/10.1074/jbc.m607577200
Abstract
No abstract availableKeywords
This publication has 42 references indexed in Scilit:
- 53BP1 Oligomerization is Independent of its Methylation by PRMT1Cell Cycle, 2005
- Saccharomyces cerevisiae Rad9 Acts as a Mec1 Adaptor to Allow Rad53 ActivationCurrent Biology, 2005
- Dynamic assembly and sustained retention of 53BP1 at the sites of DNA damage are controlled by Mdc1/NFBD1The Journal of cell biology, 2005
- Methylation of Histone H4 Lysine 20 Controls Recruitment of Crb2 to Sites of DNA DamagePublished by Elsevier ,2004
- Homo-oligomerization Is the Essential Function of the Tandem BRCT Domains in the Checkpoint Protein Crb2Journal of Biological Chemistry, 2004
- Potential Role for 53BP1 in DNA End-joining Repair through Direct Interaction with DNAJournal of Biological Chemistry, 2003
- Histone H2AX phosphorylation is dispensable for the initial recognition of DNA breaksNature Cell Biology, 2003
- Role for the BRCA1 C-terminal Repeats (BRCT) Protein 53BP1 in Maintaining Genomic StabilityPublished by Elsevier ,2003
- Budding Yeast Rad9 Is an ATP-Dependent Rad53 Activating MachinePublished by Elsevier ,2001
- Phosphorylation and Rapid Relocalization of 53BP1 to Nuclear Foci upon DNA DamageMolecular and Cellular Biology, 2001