Wataru Nomura

Professor

Hiroshima University

Japan

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About

Wataru Nomura is a Professor at Hiroshima University in Japan. His research focuses on cell cycle-dependent genome editing, CRISPR technology, and the characterization of macrophage responses to polymeric materials. Recent publications include studies on HIV latency reversing agents and the development of advanced CRISPR-Cas9 systems that enhance genome editing accuracy.

Articles (17)

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2025

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2020

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JAPAN

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Wataru Nomura

Research Interests

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About

Articles (17)

Cell cycle‐dependent regulation of CRISPR‐Cas9 repetitive activation by anti‐CRISPR and Cdt1 fusion in the CRISPRa system

Discovery of Potent DAG-Lactone Derivatives as HIV Latency Reversing Agents

SpCas9-HF1 enhances accuracy of cell cycle-dependent genome editing by increasing HDR efficiency, and by reducing off-target effects and indel rates

Effect of Two-Photon Excitation to 8-Azacoumarin Derivatives as Photolabile Protecting Groups

Characteristics of macrophage aggregates prepared by rotation culture and their response to polymeric materials

Effects of Polymeric Materials on Activation of THP-1 Cell-derived Macrophages during Differentiation Induced by PMA

Evaluation of Proinflammatory Response to Polymeric Materials Using a Macrophage Cell Line Genetically Tagged with a Luminescent Peptide

SpCas9-HF1 enhances accuracy of cell cycle-dependent genome editing by increasing HDR efficiency, and by reducing off-target effects and indel rates

<scp>Cas9‐Geminin</scp> and Cdt1‐fused <scp>anti‐CRISPR</scp> protein synergistically increase editing accuracy

The history of genome editing: advances from the interface of chemistry & biology

Discovery of a Macropinocytosis-Inducing Peptide Potentiated by Medium-Mediated Intramolecular Disulfide Formation

Molecular Switch Engineering for Precise Genome Editing.

Discovery of a Macropinocytosis‐Inducing Peptide Potentiated by Medium‐Mediated Intramolecular Disulfide Formation

Fluorescence resonance energy transfer-based screening for protein kinase C ligands using 6-methoxynaphthalene-labeled 1,2-diacylglycerol-lactones

A cell cycle-dependent CRISPR-Cas9 activation system based on an anti-CRISPR protein shows improved genome editing accuracy

TALEN-Based Chemically Inducible, Dimerization-Dependent, Sequence-Specific Nucleases

Synthesis of hydrophilic caged DAG-lactones for chemical biology applications

Collaborators (5)

Akira Otaka

Daisuke Matsumoto

Shiroh Futaki

Takuya Kobayakawa

Toshiaki Furuta

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