Associated Papers
ATM/ATR Phosphorylation of CtIP on Its Conserved Sae2-like Domain Is Required for Genotoxin-Induced DNA Resection but Dispensable for Animal Development.
Wu-Baer F et al.
Cells, 2023
ATM suppresses c-Myc overexpression in the mammary epithelium in response to estrogen.
Najnin RA et al.
Cell Reports, 2023
SUMOylation mediates CtIP's functions in DNA end resection and replication fork protection.
Locke AJ et al.
Nucleic Acids Research, 2021
Multiple DSB Resection Activities Redundantly Promote Alternative End Joining-Mediated Class Switch Recombination.
Sun X et al.
Frontiers in Cell and Developmental Biology, 2021
CDK and Mec1/Tel1-catalyzed phosphorylation of Sae2 regulate different responses to DNA damage.
Yu TY et al.
Nucleic Acids Research, 2019
CtIP is essential for early B cell proliferation and development in mice.
Liu X et al.
The Journal of Experimental Medicine, 2019
Phosphorylation of Sae2 Mediates Forkhead-associated (FHA) Domain-specific Interaction and Regulates Its DNA Repair Function.
Liang J et al.
The Journal of Biological Chemistry, 2015
CtIP maintains stability at common fragile sites and inverted repeats by end resection-independent endonuclease activity.
Wang H et al.
Molecular Cell, 2014
Catalytic and noncatalytic roles of the CtIP endonuclease in double-strand break end resection.
Makharashvili N et al.
Molecular Cell, 2014
Activation of DSB processing requires phosphorylation of CtIP by ATR.
Peterson SE et al.
Molecular Cell, 2013
The interaction of CtIP and Nbs1 connects CDK and ATM to regulate HR-mediated double-strand break repair.
Wang H et al.
Plos Genetics, 2013
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