His scientific interests lie mostly in DNA replication, Molecular biology, DNA polymerase delta, DNA clamp and DNA polymerase II. His work in DNA replication is not limited to one particular discipline; it also encompasses Cell biology. His Cell biology research is multidisciplinary, relying on both Processivity, dnaN, DNA synthesis, Proliferating cell nuclear antigen and Monoubiquitination.
His research in Molecular biology intersects with topics in Genetics, Gene, DNA, DNA polymerase and Hepatitis B virus. His DNA polymerase delta research incorporates themes from Replication factor C, Prokaryotic DNA replication and Eukaryotic DNA replication. His work carried out in the field of Origin recognition complex brings together such families of science as Replication protein A, DNA replication factor CDT1, Ubiquitin and Licensing factor.
Toshiki Tsurimoto mostly deals with DNA replication, Molecular biology, Cell biology, Eukaryotic DNA replication and Origin recognition complex. Toshiki Tsurimoto has included themes like DNA polymerase delta, Replication protein A and DNA polymerase in his DNA replication study. As a part of the same scientific study, Toshiki Tsurimoto usually deals with the DNA polymerase delta, concentrating on DNA clamp and frequently concerns with dnaN.
His Molecular biology study combines topics in areas such as Mutant, DNA, Proliferating cell nuclear antigen, DNA polymerase II and Hepatitis B virus. His study in Cell biology is interdisciplinary in nature, drawing from both Chromatin and DNA repair. His Origin recognition complex study integrates concerns from other disciplines, such as Origin of replication, Licensing factor, ORC1, DNA replication factor CDT1 and Cell cycle.
Toshiki Tsurimoto mainly investigates DNA replication, Genetics, DNA polymerase, Cell biology and Molecular biology. When carried out as part of a general DNA replication research project, his work on Origin recognition complex is frequently linked to work in C-terminus, therefore connecting diverse disciplines of study. His DNA polymerase study combines topics from a wide range of disciplines, such as Replication factor C, Proliferating cell nuclear antigen, DNA damage and DNA synthesis.
The concepts of his Proliferating cell nuclear antigen study are interwoven with issues in DNA polymerase delta and DNA clamp. His Cell biology research is multidisciplinary, incorporating perspectives in Budding yeast, Single-stranded DNA binding, DNA and Fight-or-flight response. The Molecular biology study combines topics in areas such as DNA polymerase II and Mutant.
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Rad18 guides polη to replication stalling sites through physical interaction and PCNA monoubiquitination
Kenji Watanabe;Satoshi Tateishi;Michio Kawasuji;Toshiki Tsurimoto.
The EMBO Journal (2004)
Regulation of DNA-replication origins during cell-cycle progression.
Katsuhiko Shirahige;Yuji Hori;Katsuya Shiraishi;Minoru Yamashita.
Nature (1998)
Replication factors required for SV40 DNA replication in vitro. I. DNA structure-specific recognition of a primer-template junction by eukaryotic DNA polymerases and their accessory proteins.
T Tsurimoto;B Stillman.
Journal of Biological Chemistry (1991)
Sequential initiation of lagging and leading strand synthesis by two different polymerase complexes at the SV40 DNA replication origin.
Toshiki Tsurimoto;Thomas Melendy;Bruce Stillman.
Nature (1990)
Two E3 ubiquitin ligases, SCF-Skp2 and DDB1-Cul4, target human Cdt1 for proteolysis.
Hideo Nishitani;Nozomi Sugimoto;Vassilis Roukos;Yohsuke Nakanishi.
The EMBO Journal (2006)
Replication factors required for SV40 DNA replication in vitro. II. Switching of DNA polymerase alpha and delta during initiation of leading and lagging strand synthesis.
Toshiki Tsurimoto;B. Stillman.
Journal of Biological Chemistry (1991)
Functions of replication factor C and proliferating-cell nuclear antigen: functional similarity of DNA polymerase accessory proteins from human cells and bacteriophage T4.
Toshiki Tsurimoto;Bruce Stillman.
Proceedings of the National Academy of Sciences of the United States of America (1990)
CDK Inhibitor p21 Is Degraded by a Proliferating Cell Nuclear Antigen-coupled Cul4-DDB1Cdt2 Pathway during S Phase and after UV Irradiation
Hideo Nishitani;Hideo Nishitani;Yasushi Shiomi;Hiroka Iida;Masato Michishita.
Journal of Biological Chemistry (2008)
Multiple replication factors augment DNA synthesis by the two eukaryotic DNA polymerases, alpha and delta.
Toshiki Tsurimoto;B. Stillman.
The EMBO Journal (1989)
PCNA binding proteins.
Toshiki Tsurimoto.
Frontiers in Bioscience (1999)
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