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Resection of DNA double-strand breaks activates Mre11- Rad50- Nbs1- and Rad9- Hus1- Rad1-dependent mechanisms that redundantly promote ATR checkpoint activation and end processing in Xenopus egg extracts. , Tatsukawa K., Nucleic Acids Res. April 12, 2024; 52 (6): 3146-3163.
POLθ prevents MRE11- NBS1- CtIP-dependent fork breakage in the absence of BRCA2/RAD51 by filling lagging-strand gaps. , Mann A., Mol Cell. November 17, 2022; 82 (22): 4218-4231.e8.
MRN-dependent and independent pathways for recruitment of TOPBP1 to DNA double-strand breaks. , Montales K., PLoS One. August 2, 2022; 17 (8): e0271905.
ZC3HC1 Is a Novel Inherent Component of the Nuclear Basket, Resident in a State of Reciprocal Dependence with TPR. , Gunkel P., Cells. July 30, 2021; 10 (8):
Protein phosphatase 1 and phosphatase 1 nuclear targeting subunit-dependent regulation of DNA-dependent protein kinase and non-homologous end joining. , Zhu S., Nucleic Acids Res. October 13, 2017; 45 (18): 10583-10594.
Mdc1 modulates the interaction between TopBP1 and the MRN complex during DNA damage checkpoint responses. , Choi SH., Biochem Biophys Res Commun. October 7, 2016; 479 (1): 5-11.
Xenopus Mcm10 is a CDK-substrate required for replication fork stability. , Chadha GS., Cell Cycle. August 17, 2016; 15 (16): 2183-2195.
The Mre11- Rad50- Nbs1 (MRN) complex has a specific role in the activation of Chk1 in response to stalled replication forks. , Lee J ., Mol Biol Cell. May 1, 2013; 24 (9): 1343-53.
A role for the MRN complex in ATR activation via TOPBP1 recruitment. , Duursma AM., Mol Cell. April 11, 2013; 50 (1): 116-22.
The MRN- CtIP pathway is required for metaphase chromosome alignment. , Rozier L., Mol Cell. March 28, 2013; 49 (6): 1097-107.
Dgp71WD is required for the assembly of the acentrosomal Meiosis I spindle, and is not a general targeting factor for the γ-TuRC. , Reschen RF., Biol Open. May 15, 2012; 1 (5): 422-9.
Analysis of MRE11's function in the 5'-->3' processing of DNA double-strand breaks. , Liao S., Nucleic Acids Res. May 1, 2012; 40 (10): 4496-506.
Time-dependent predominance of nonhomologous DNA end-joining pathways during embryonic development in mice. , Chiruvella KK., J Mol Biol. March 30, 2012; 417 (3): 197-211.
Role for Rif1 in the checkpoint response to damaged DNA in Xenopus egg extracts. , Kumar S ., Cell Cycle. March 15, 2012; 11 (6): 1183-94.
Essential roles of Xenopus TRF2 in telomere end protection and replication. , Muraki K., Genes Cells. June 1, 2011; 16 (6): 728-39.
CtIP interacts with TopBP1 and Nbs1 in the response to double-stranded DNA breaks (DSBs) in Xenopus egg extracts. , Ramírez-Lugo JS., Cell Cycle. February 1, 2011; 10 (3): 469-80.
Xenopus DNA2 is a helicase/nuclease that is found in complexes with replication proteins And-1/ Ctf4 and Mcm10 and DSB response proteins Nbs1 and ATM. , Wawrousek KE., Cell Cycle. March 15, 2010; 9 (6): 1156-66.
The Mre11/ Rad50/ Nbs1 complex functions in resection-based DNA end joining in Xenopus laevis. , Taylor EM., Nucleic Acids Res. January 1, 2010; 38 (2): 441-54.
CtIP links DNA double-strand break sensing to resection. , You Z., Mol Cell. December 25, 2009; 36 (6): 954-69.
The Mre11- Rad50- Nbs1 complex mediates activation of TopBP1 by ATM. , Yoo HY., Mol Biol Cell. May 1, 2009; 20 (9): 2351-60.
Mre11- Rad50- Nbs1-dependent processing of DNA breaks generates oligonucleotides that stimulate ATM activity. , Jazayeri A., EMBO J. July 23, 2008; 27 (14): 1953-62.
Rapid activation of ATM on DNA flanking double-strand breaks. , You Z., Nat Cell Biol. November 1, 2007; 9 (11): 1311-8.
ATM and ATR promote Mre11 dependent restart of collapsed replication forks and prevent accumulation of DNA breaks. , Trenz K., EMBO J. April 19, 2006; 25 (8): 1764-74.
Repair of double-strand breaks by nonhomologous end joining in the absence of Mre11. , Di Virgilio M., J Cell Biol. December 5, 2005; 171 (5): 765-71.
ATM activation and its recruitment to damaged DNA require binding to the C terminus of Nbs1. , You Z., Mol Cell Biol. July 1, 2005; 25 (13): 5363-79.
Probing spindle assembly mechanisms with monastrol, a small molecule inhibitor of the mitotic kinesin, Eg5. , Kapoor TM., J Cell Biol. September 4, 2000; 150 (5): 975-88.