Mdc1 modulates the interaction between TopBP1 and the MRN complex during DNA damage checkpoint responses
Author:
Funder
National Research Foundation of Korea
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference28 articles.
1. Toward maintaining the genome: DNA damage and replication checkpoints;Nyberg;Annu. Rev. Genet.,2002
2. Molecular mechanisms of mammalian DNA repair and the DNA damage checkpoints;Sancar;Annu. Rev. Biochem.,2004
3. The ATM-mediated DNA-damage response: taking shape;Shiloh;Trends Biochem. Sci.,2006
4. Cell cycle checkpoint signaling through the ATM and ATR kinases;Abraham;Genes Dev.,2001
5. How cells activate ATR;Kumagai;Cell Cycle,2006
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1. MRN-dependent and independent pathways for recruitment of TOPBP1 to DNA double-strand breaks;PLOS ONE;2022-08-02
2. Delineation of a minimal topoisomerase II binding protein 1 for regulated activation of ATR at DNA double-strand breaks;Journal of Biological Chemistry;2022-07
3. Proline-serine-threonine-repeat region of MDC1 mediates Chk1 phosphorylation and the DNA double-strand break repair;The International Journal of Biochemistry & Cell Biology;2022-02
4. Functions of TopBP1 in preserving genome integrity during mitosis;Seminars in Cell & Developmental Biology;2021-05
5. Structure-function analysis of TOPBP1’s role in ATR signaling using the DSB-mediated ATR activation in Xenopus egg extracts (DMAX) system;Scientific Reports;2021-01-11
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