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The structure of ends determines the pathway choice and Mre11 nuclease dependency of DNA double-strand break repair. , Liao S., Nucleic Acids Res. July 8, 2016; 44 (12): 5689-701.
DNA double-strand breaks with 5' adducts are efficiently channeled to the DNA2-mediated resection pathway. , Tammaro M., Nucleic Acids Res. January 8, 2016; 44 (1): 221-31.
Purified E255L mutant SERCA1a and purified PfATP6 are sensitive to SERCA-type inhibitors but insensitive to artemisinins. , Cardi D., J Biol Chem. August 20, 2010; 285 (34): 26406-16.
G2 phase chromatin lacks determinants of replication timing. , Lu J., J Cell Biol. June 14, 2010; 189 (6): 967-80.
The highly conserved nuclear lamin Ig-fold binds to PCNA: its role in DNA replication. , Shumaker DK., J Cell Biol. April 21, 2008; 181 (2): 269-80.
Analysis of terminal sugar moieties and species-specificities of acrosome reaction-inducing substance in Xenopus (ARISX). , Ueda Y., Dev Growth Differ. September 1, 2007; 49 (7): 591-601.
Spatial distribution and specification of mammalian replication origins during G1 phase. , Li F., J Cell Biol. April 28, 2003; 161 (2): 257-66.
Oligonucleotide trapping method for purification of transcription factors. , Gadgil H., J Chromatogr A. August 9, 2002; 966 (1-2): 99-110.
The replication timing program of the Chinese hamster beta-globin locus is established coincident with its repositioning near peripheral heterochromatin in early G1 phase. , Li F., J Cell Biol. July 23, 2001; 154 (2): 283-92.