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Nucleic Acids Research|June 17, 2004
The recognition and modification sites for the bacterial type I restriction systems KpnAI, StySEAI, StySENI and StySGIJulie K A Kasarjian, Masumi Hidaka, Takashi Horiuchi, et al.
The Journal of Biological Chemistry|October 16, 2004
Cooperation of the N-terminal Helicase and C-terminal endonuclease activities of Archaeal Hef protein in processing stalled replication forksKayoko Komori, Masumi Hidaka, Takashi Horiuchi, et al.
The Journal of Biological Chemistry|December 18, 2019
SMARCAD1-mediated recruitment of the DNA mismatch repair protein MutLα to MutSα on damaged chromatin induces apoptosis in human cellsYukimasa Takeishi, Ryosuke Fujikane, Mihoko Rikitake, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|April 16, 2003
Fate of DNA replication fork encountering a single DNA lesion during oriC plasmid DNA replication in vitroKumiko Higuchi, Tsutomu Katayama, Shigenori Iwai, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|January 20, 2020
MLH1-mediated recruitment of FAN1 to chromatin for the induction of apoptosis triggered by O6 -methylguanineMihoko Rikitake, Ryosuke Fujikane, Yuko Obayashi, et al.
Carcinogenesis|September 21, 2007
Modes of actions of two types of anti-neoplastic drugs, dacarbazine and ACNU, to induce apoptosisMasayuki Sanada, Masumi Hidaka, Yasumitsu Takagi, et al.
Mutation Research|April 26, 2022
Novel plasmids for the fluorescence-based evaluation of DNA mismatch repair in human cellsArato Takedachi, Erina Matsuishi, Shouji Mizusaki, et al.
Molecular Cell|April 5, 2002
Human origin recognition complex large subunit is degraded by ubiquitin-mediated proteolysis after initiation of DNA replicationJuan Méndez, X Helena Zou-Yang, So-Young Kim, et al.
DNA Repair|January 3, 2012
Activation of AMP-activated protein kinase by MAPO1 and FLCN induces apoptosis triggered by alkylated base mismatch in DNATeik How Lim, Ryosuke Fujikane, Shiori Sano, et al.
Experimental Cell Research|February 26, 2019
Differential genomic destabilisation in human cells with pathogenic MSH2 mutations introduced by genome editingGenki Hayashida, Seijiro Shioi, Kyoko Hidaka, et al.
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