Papers associated with spermatozoon (and mcm7)

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	The p97 segregase cofactor Ubxn7 facilitates replisome disassembly during S-phase., Tarcan Z., J Biol Chem. August 1, 2022; 298 (8): 102234.
	SSRP1-mediated histone H1 eviction promotes replication origin assembly and accelerated development., Falbo L., Nat Commun. March 12, 2020; 11 (1): 1345.
	Mitotic replisome disassembly depends on TRAIP ubiquitin ligase activity., Priego Moreno S., Life Sci Alliance. April 12, 2019; 2 (2):
	Mitotic CDK Promotes Replisome Disassembly, Fork Breakage, and Complex DNA Rearrangements., Deng L., Mol Cell. March 7, 2019; 73 (5): 915-929.e6.
	Mitotic entry drives replisome disassembly at stalled replication forks., Hashimoto Y., Biochem Biophys Res Commun. November 17, 2018; 506 (1): 108-113.
	The High-Affinity Interaction between ORC and DNA that Is Required for Replication Licensing Is Inhibited by 2-Arylquinolin-4-Amines., Gardner NJ., Cell Chem Biol. August 17, 2017; 24 (8): 981-992.e4.
	CUL-2LRR-1 and UBXN-3 drive replisome disassembly during DNA replication termination and mitosis., Sonneville R., Nat Cell Biol. May 1, 2017; 19 (5): 468-479.
	Reversal of DDK-Mediated MCM Phosphorylation by Rif1-PP1 Regulates Replication Initiation and Replisome Stability Independently of ATR/Chk1., Alver RC., Cell Rep. March 7, 2017; 18 (10): 2508-2520.
	Xenopus Mcm10 is a CDK-substrate required for replication fork stability., Chadha GS., Cell Cycle. August 17, 2016; 15 (16): 2183-2195.
	Structure of human Cdc45 and implications for CMG helicase function., Simon AC., Nat Commun. May 18, 2016; 7 11638.
	The mechanism of DNA replication termination in vertebrates., Dewar JM., Nature. September 17, 2015; 525 (7569): 345-50.
	DNA topoisomerase IIα controls replication origin cluster licensing and firing time in Xenopus egg extracts., Gaggioli V., Nucleic Acids Res. August 1, 2013; 41 (15): 7313-31.
	DNA polymerase κ-dependent DNA synthesis at stalled replication forks is important for CHK1 activation., Bétous R., EMBO J. July 31, 2013; 32 (15): 2172-85.
	Mcm8 and Mcm9 form a dimeric complex in Xenopus laevis egg extract that is not essential for DNA replication initiation., Gambus A., Cell Cycle. April 15, 2013; 12 (8): 1225-32.
	GEMC1 is a TopBP1-interacting protein required for chromosomal DNA replication., Balestrini A., Nat Cell Biol. May 1, 2010; 12 (5): 484-91.
	Tipin/Tim1/And1 protein complex promotes Pol alpha chromatin binding and sister chromatid cohesion., Errico A., EMBO J. December 2, 2009; 28 (23): 3681-92.
	Replication initiation complex formation in the absence of nuclear function in Xenopus., Krasinska L., Nucleic Acids Res. April 1, 2009; 37 (7): 2238-48.
	Cdc7-Drf1 kinase links chromosome cohesion to the initiation of DNA replication in Xenopus egg extracts., Takahashi TS., Genes Dev. July 15, 2008; 22 (14): 1894-905.
	Plx1 is required for chromosomal DNA replication under stressful conditions., Trenz K., EMBO J. March 19, 2008; 27 (6): 876-85.
	Excess Mcm2-7 license dormant origins of replication that can be used under conditions of replicative stress., Woodward AM., J Cell Biol. June 5, 2006; 173 (5): 673-83.
	A Xenopus Dbf4 homolog is required for Cdc7 chromatin binding and DNA replication., Jares P., BMC Mol Biol. June 28, 2004; 5 5.
	The role of Cdc6 in ensuring complete genome licensing and S phase checkpoint activation., Oehlmann M., J Cell Biol. April 26, 2004; 165 (2): 181-90.
	DNA damage-induced replication arrest in Xenopus egg extracts., Stokes MP., J Cell Biol. October 27, 2003; 163 (2): 245-55.
	The Xenopus Xmus101 protein is required for the recruitment of Cdc45 to origins of DNA replication., Van Hatten RA., J Cell Biol. November 25, 2002; 159 (4): 541-7.
	Reconstitution of licensed replication origins on Xenopus sperm nuclei using purified proteins., Gillespie PJ., BMC Biochem. January 1, 2001; 2 15.
	XMCM7, a novel member of the Xenopus MCM family, interacts with XMCM3 and colocalizes with it throughout replication., Romanowski P., Proc Natl Acad Sci U S A. September 17, 1996; 93 (19): 10189-94.

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