Updated on 2025/07/28

写真a

 
CHUMAN Yoshiro
 
Organization
Academic Assembly Institute of Science and Technology Fundamental Sciences Professor
Faculty of Science Department of Science Professor
Graduate School of Science and Technology Fundamental Sciences Professor
. Research Professor
Title
Professor
External link

Degree

  • 博士(理学) ( 2001.3   九州大学 )

Research Interests

  • Biochemistry

  • aptamer

  • peptide

  • phosphorylation

  • phosphatase

  • 抗体

  • cancer

  • 抗癌剤

  • 生化学

  • バイオセンサー

  • バイオマテリアル

  • 生物化学

  • Functional biochemistry

  • Structural biochemistry

  • 刺激応答性分子

Research Areas

  • Nanotechnology/Materials / Chemistry and chemical methodology of biomolecules

  • Nanotechnology/Materials / Green sustainable chemistry and environmental chemistry

  • Life Science / Tumor diagnostics and therapeutics

  • Nanotechnology/Materials / Bio chemistry

  • Life Science / Functional biochemistry

Research History (researchmap)

  • Niigata University   Professor

    2024.10

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  • Niigata University   Institute for Research Promotion   Research Professor

    2021.9 - 2024.9

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  • Niigata University   Faculty of Science, Department of Science   Associate Professor

    2017.4 - 2024.9

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  • Niigata University   Faculty of Science, Department of Chemistry   Associate Professor

    2013.11 - 2017.3

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  • Hokkaido University   Faculty of Science   Assistant Professor

    2007.4 - 2013.10

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  • Hokkaido University   Research Assistant

    2001.11 - 2007.3

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  • 米国国立衛生研究所(NIH)国立ガン研究所(NCI)   visiting fellow

    2001.5 - 2003.10

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  • イタリア国立衛生研究所・分子薬理学研究室   科研費国際学術共同研究協力員

    1999.9 - 1999.10

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  • イタリア国立衛生研究所・分子薬理学研究室   科研費国際学術共同研究協力員

    1998.9 - 1998.12

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  • 日本学術振興会特別研究員(DC1)

    1998.4 - 2001.3

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  • Postdoctoral Fellowships of Japan Society for the Promotion of Science

    1998 - 2001

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  • イタリア国立衛生研究所・分子薬理学研究室   科研費国際学術共同研究協力員

    1997.9 - 1997.10

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Research History

  • Niigata University   Fundamental Sciences, Institute of Science and Technology, Academic Assembly   Professor

    2024.10

  • Niigata University   Professor

    2024.10

  • Niigata University   Fundamental Sciences, Graduate School of Science and Technology   Professor

    2024.10

  • Niigata University   Department of Science, Faculty of Science   Professor

    2024.10

  • Niigata University   Faculty of Science Department of Science   Associate Professor

    2017.4 - 2024.9

  • Niigata University   Abolition organization Organic and Biological Chemistry   Associate Professor

    2013.11 - 2017.3

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Education

  • Kyushu University   九州大学理学部化学科卒業 学士(理学)

    1996.3

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  • Kyushu University   大学院理学研究科化学専攻修士課程修了 修士(理学)

    1998.3

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  • Kyushu University   Graduate School of Sciences   博士課程修了 博士(理学)

    2001.3

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Professional Memberships

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Committee Memberships

  • Bentham Science publishers   Bentham Ambassador  

    2019   

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    Committee type:Academic society

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  • 新潟生化学懇話会   幹事  

    2019   

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    Committee type:Academic society

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  • 文部科学省   専門調査員  

    2019   

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    Committee type:Government

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  • The Japanese peptide society   10th International Peptide Symposium International Program Committee  

    2018   

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  • 日本化学会   関東支部新潟地域懇談会事務局  

    2017   

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  • 日本ホスファターゼ学会   世話人  

    2016   

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  • N-hybrid   世話人  

    2016   

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  • 日本ペプチド学会   PNJ編集委員・HP委員  

    2014 - 2023   

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  • 日本ペプチド学会   第40回若手ペプチド夏の勉強会 代表世話人  

    2007   

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Studying abroad experiences

  • 米国国立衛生研究所(NIH)国立ガン研究所(NCI)   博士研究員

    2001.5 - 2003.10

  • イタリア国立衛生研究所・分子薬理学研究室   科研費国際学術共同研究協力員

    1999.9 - 1999.10

  • イタリア国立衛生研究所・分子薬理学研究室   科研費国際学術共同研究協力員

    1998.9 - 1998.12

  • イタリア国立衛生研究所・分子薬理学研究室   科研費国際学術共同研究協力員

    1997.9 - 1997.10

 

Papers

  • Identification of Inhibitors of the Disease-Associated Protein Phosphatase Scp1 Using Antibody Mimetic Molecules Invited Reviewed

    Tamaki Kobayashi, Kazuki Yamazaki, Junki Shinada, Masataka Mizunuma, Kazuhiro Furukawa, Yoshiro Chuman

    Int. J. Mol. Sci.   25 ( 7 )   3737 - 3737   2024.3

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    Authorship:Corresponding author   Publishing type:Research paper (scientific journal)   Publisher:MDPI AG  

    Protein phosphorylation is a prevalent translational modification, and its dysregulation has been implicated in various diseases, including cancer. Despite its significance, there is a lack of specific inhibitors of the FCP/SCP-type Ser/Thr protein phosphatase Scp1, characterized by high specificity and affinity. In this study, we focused on adnectin, an antibody-mimetic protein, aiming to identify Scp1-specific binding molecules with a broad binding surface that target the substrate-recognition site of Scp1. Biopanning of Scp1 was performed using an adnectin-presenting phage library with a randomized FG loop. We succeeded in identifying FG-1Adn, which showed high affinity and specificity for Scp1. Ala scanning analysis of the Scp1-binding sequence in relation to the FG-1 peptide revealed that hydrophobic residues, including aromatic amino acids, play important roles in Scp1 recognition. Furthermore, FG-1Adn was found to co-localize with Scp1 in cells, especially on the plasma membrane. In addition, Western blotting analysis showed that FG-1Adn increased the phosphorylation level of the target protein of Scp1 in cells, indicating that FG-1Adn can inhibit the function of Scp1. These results suggest that FG-1Adn can be used as a specific inhibitor of Scp1.

    DOI: 10.3390/ijms25073737

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  • Bilayer Hydrogel Composed of Elastin-Mimetic Polypeptides as a Bio-Actuator with Bidirectional and Reversible Bending Behaviors Reviewed

    Rui Kamada, Hiromitsu Miyazaki, Jose Isagani Janairo, Yoshiro Chuman, Kazuyasu Sakaguchi

    Molecules   28 ( 13 )   5274   2023.7

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    DOI: 10.3390/molecules28135274

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  • Development of Mn2+-Specific Biosensor Using G-Quadruplex-Based DNA Invited Reviewed

    Masataka Mizunuma, Mirai Suzuki, Tamaki Kobayashi, Yuki Hara, Atsushi Kaneko, Kazuhiro Furukawa, Yoshiro Chuman

    Int. J. Mol. Sci.   24 ( 14 )   11556 - 11556   2023.7

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    Authorship:Corresponding author   Publishing type:Research paper (scientific journal)   Publisher:MDPI AG  

    Metal ions are used in various situations in living organisms and as a part of functional materials. Since the excessive intake of metal ions can cause health hazards and environmental pollution, the development of new molecules that can monitor metal ion concentrations with high sensitivity and selectivity is strongly desired. DNA can form various structures, and these structures and their properties have been used in a wide range of fields, including materials, sensors, and drugs. Guanine-rich sequences respond to metal ions and form G-quadruplex structures and G-wires, which are the self-assembling macromolecules of G-quadruplex structures. Therefore, guanine-rich DNA can be applied to a metal ion-detection sensor and functional materials. In this study, the IRDAptamer library originally designed based on G-quadruplex structures was used to screen for Mn2+, which is known to induce neurodegenerative diseases. Circular dichroism and fluorescence analysis using Thioflavin T showed that the identified IRDAptamer sequence designated MnG4C1 forms a non-canonical G-quadruplex structure in response to low concentrations of Mn2+. A serum resistance and thermostability analysis revealed that MnG4C1 acquired stability in a Mn2+-dependent manner. A Förster resonance energy transfer (FRET) system using fluorescent molecules attached to the termini of MnG4C1 showed that FRET was effectively induced based on Mn2+-dependent conformational changes, and the limit of detection (LOD) was 0.76 µM for Mn2+. These results suggested that MnG4C1 can be used as a novel DNA-based Mn2+-detecting molecule.

    DOI: 10.3390/ijms241411556

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  • Development of Antibody-like Proteins Targeting the Oncogenic Ser/Thr Protein Phosphatase PPM1D Reviewed

    Megumi Ikeura, Hiroto Tashiro, Yuka Yamagata, Hikaru Saito, Tamaki Kobayashi, Masataka Mizunuma, Kazuki Yamazaki, Keisuke Baba, Kazuhiro Furukawa, Yoshiro Chuman

    Processes   10 ( 8 )   1501 - 1501   2022.7

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    Authorship:Corresponding author   Publishing type:Research paper (scientific journal)   Publisher:MDPI AG  

    PPM1D, a protein Ser/Thr phosphatase, is overexpressed in various cancers and functions as an oncogenic protein by inactivating the p53 pathway. Therefore, molecules that bind PPM1D are expected to be useful anti-cancer agents. In this study, we constructed a phage display library based on the antibody-like small molecule protein adnectin and screened for PPM1D-specific binding molecules. We identified two adnectins, PMDB-1 and PMD-24, that bind PPM1D specific B-loop and PPM1D430 as targets, respectively. Specificity analyses of these recombinant proteins using other Ser/Thr protein phosphatases showed that these molecules bind to only PPM1D. Expression of PMDB-1 in breast cancer-derived MCF-7 cells overexpressing endogenous PPM1D stabilized p53, indicating that PMDB-1 functions as an inhibitor of PPM1D. Furthermore, MTT assay exhibited that MCF-7 cells expressing PMDB-1 showed inhibition of cell proliferation. These data suggest that the adnectin PMDB-1 identified in this study can be used as a lead compound for anti-cancer drugs targeting intracellular PPM1D.

    DOI: 10.3390/pr10081501

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  • Methods for Identification of Substrates/Inhibitors of FCP/SCP Type Protein Ser/Thr Phosphatases

    Masataka Mizunuma, Atsushi Kaneko, Shunta Imai, Kazuhiro Furukawa, Yoshiro Chuman

    Processes   8 ( 12 )   1598 - 1598   2020.12

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    Authorship:Corresponding author   Publishing type:Research paper (scientific journal)   Publisher:MDPI AG  

    Protein phosphorylation is the most widespread type of post-translational modification and is properly controlled by protein kinases and phosphatases. Regarding the phosphorylation of serine (Ser) and threonine (Thr) residues, relatively few protein Ser/Thr phosphatases control the specific dephosphorylation of numerous substrates, in contrast with Ser/Thr kinases. Recently, protein Ser/Thr phosphatases were reported to have rigid substrate recognition and exert various biological functions. Therefore, identification of targeted proteins by individual protein Ser/Thr phosphatases is crucial to clarify their own biological functions. However, to date, information on the development of methods for identification of the substrates of protein Ser/Thr phosphatases remains scarce. In turn, substrate-trapping mutants are powerful tools to search the individual substrates of protein tyrosine (Tyr) phosphatases. This review focuses on the development of novel methods for the identification of Ser/Thr phosphatases, especially small C-terminal domain phosphatase 1 (Scp1), using peptide-displayed phage library with AlF4−/BeF3−, and discusses the identification of putative inhibitors.

    DOI: 10.3390/pr8121598

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  • Development of Specific Inhibitors for Oncogenic Phosphatase PPM1D by Using Ion-Responsive DNA Aptamer Library Reviewed

    Atsushi Kaneko, Miyuu Watari, Masataka Mizunuma, Hikaru Saito, Kazuhiro Furukawa, Yoshiro Chuman

    Catalysts   10 ( 10 )   1153 - 1153   2020.10

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    (1) Background: Ser/Thr protein phosphatase PPM1D is an oncogenic protein. In normal cells, however, PPM1D plays essential roles in spermatogenesis and immune response. Hence, it is necessary to develop novel PPM1D inhibitors without side effects on normal cells. Stimuli-responsive molecules are suitable for the spatiotemporal regulation of inhibitory activity. (2) Methods: In this study, we designed an ion-responsive DNA aptamer library based on G-quadruplex DNA that can change its conformation and function in response to monovalent cations. (3) Results: Using this library, we identified the PPM1D specific inhibitor M1D-Q5F aptamer. The M1D-Q5F aptamer showed anti-cancer activity against breast cancer MCF7 cells. Interestingly, the induction of the structural change resulting in the formation of G-quadruplex upon stimulation by monovalent cations led to the enhancement of the inhibitory activity and binding affinity of M1D-Q5F. (4) Conclusions: These data suggest that the M1D-Q5F aptamer may act as a novel stimuli-responsive anti-cancer agent.

    DOI: 10.3390/catal10101153

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  • Identification of a Specific Inhibitor of Human Scp1 Phosphatase Using the Phosphorylation Mimic Phage Display Method Reviewed

    Yoshida, T, Yamazaki, K, Imai, S, Banno, A, Kaneko, A, Furukawa, K, Chuman, Y

    Catalysts   9 ( 10 )   842   2019.10

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    Authorship:Corresponding author   Language:English  

    DOI: 10.3390/catal9100842

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  • PPM1D enhances retinoic acid-induced differentiation in human embryonic carcinoma cell line Reviewed International journal

    J. Biochem

    J. Biochem.   165 ( 6 )   471 - 477   2019

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    The protein phosphatase PPM1D (Wip1) was originally identified as a p53 target product. Activation of PPM1D through various mechanism promotes the tumorigenic potential of various cancers by suppressing p53 and other DNA damage response proteins. New functions of PPM1D have recently been revealed in physiological processes such as cell differentiation. However, the regulatory mechanisms of signalling pathway to maintain stemness and induce cell differentiation are still unclear. Here we report that PPM1D modulates retinoic acid (RA) signalling. PPM1D knockdown resulted in decreased alkaline phosphatase activity of the human teratocarcinoma cell line NT2/D1. Inhibition of PPM1D-induced cell differentiation and decreased gene expression of the stem cell marker Oct-4 (POU5F1). RA-induced cell differentiation was promoted by reducing PPM1D activity. RA treatment elicited activation of the MEK-ERK pathway and induced rapid and transient activation of the extracellular signal-regulated kinase 1/2 (ERK-1/2). PPM1D dephosphorylated a phosphopeptide with the TEY motif in ERK-1/2 in vitro. Moreover, phosphorylation of ERK-1/2 was facilitated by PPM1D inhibition. Our study shows that PPM1D plays an important role in maintaining the undifferentiation state and a new function in RA-induced ERK regulation and cell differentiation.

    DOI: 10.1093/jb/mvy119

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  • Development of a substrate identification method for human Scp1 phosphatase using phosphorylation mimic phage display Reviewed

    Kodai Otsubo, Takashi Yoneda, Atsushi Kaneko, Seiya Yagi, Kazuhiro Furukawa, Yoshiro Chuman

    Protein and Peptide Letters   25 ( 1 )   76 - 83   2018.1

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    Authorship:Corresponding author   Language:English   Publisher:Bentham Science Publishers B.V.  

    DOI: 10.2174/0929866525666171206114913

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  • Non-farnesylated B-type lamin can tether chromatin inside the nucleus and its chromatin interaction requires the Ig-fold region Reviewed

    Ryo Uchino, Shin Sugiyama, Motoi Katagiri, Yoshiro Chuman, Kazuhiro Furukawa

    CHROMOSOMA   126 ( 1 )   125 - 144   2017.2

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    DOI: 10.1007/s00412-016-0581-x

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  • PPM1D controls nucleolar formation by up-regulating phosphorylation of nucleophosmin Reviewed

    Yuuki Kozakai, Rui Kamada, Junya Furuta, Yuhei Kiyota, Yoshiro Chuman, Kazuyasu Sakaguchi

    SCIENTIFIC REPORTS   6   33272   2016.9

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    DOI: 10.1038/srep33272

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  • Patterning nanofibrils through the templated growth of multiple modified amyloid peptides Reviewed

    Hiroki Sakai, Ken Watanabe, Fuki Kudoh, Rui Kamada, Yoshiro Chuman, Kazuyasu Sakaguchi

    SCIENTIFIC REPORTS   6   31993   2016.8

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    DOI: 10.1038/srep31993

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  • Effective Cellular Morphology Analysis for Differentiation Processes by a Fluorescent 1,3a,6a-Triazapentalene Derivative Probe in Live Cells Reviewed

    Rui Kamada, Fumi Tano, Fuki Kudoh, Nozomi Kimura, Yoshiro Chuman, Ayumi Osawa, Kosuke Namba, Keiji Tanino, Kazuyasu Sakaguchi

    PLOS ONE   11 ( 8 )   e0160625   2016.8

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    DOI: 10.1371/journal.pone.0160625

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  • Novel inhibitors targeting PPM1D phosphatase potently suppress cancer cell proliferation Reviewed

    Sari Ogasawara, Yuhei Kiyota, Yoshiro Chuman, Ayano Kowata, Fumihiko Yoshimura, Keiji Tanino, Rui Kamada, Kazuyasu Sakaguchi

    BIOORGANIC & MEDICINAL CHEMISTRY   23 ( 19 )   6246 - 6249   2015.10

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    DOI: 10.1016/j.bmc.2015.08.042

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  • Synthesis of yellow and red fluorescent 1,3a, 6a-triazapentalenes and the theoretical investigation of their optical properties Reviewed

    Kosuke Namba, Ayumi Osawa, Akira Nakayama, Akane Mera, Fumi Tano, Yoshiro Chuman, Eri Sakuda, Tetsuya Taketsugu, Kazuyasu Sakaguchi, Noboru Kitamura, Keiji Tanino

    CHEMICAL SCIENCE   6 ( 2 )   1083 - 1093   2015

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    DOI: 10.1039/c4sc02780a

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  • Function of Proto-oncogene Product PPM1D and Development of PPM1D Inhibitors for Cancer Chemotherapy Reviewed

    Kamada R, Chuman Y, Kozakai Y, Sakaguchi K

    Seikagaku. The Journal of Japanese Biochemical Society   87 ( 5 )   531 - 538   2015

  • Secreted Frizzled-related protein potentiation versus inhibition of Wnt3a/beta-catenin signaling Reviewed

    Charles P. Xavier, Maria Melikova, Yoshiro Chuman, Aykut Ueren, Bolormaa Baljinnyam, Jeffrey S. Rubin

    CELLULAR SIGNALLING   26 ( 1 )   94 - 101   2014.1

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    DOI: 10.1016/j.cellsig.2013.09.016

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  • Formation of functionalized nanowires by control of self-assembly using multiple modified amyloid peptides Reviewed

    Hiroki Sakai, Ken Watanabe, Yuya Asanomi, Yumiko Kobayashi, Yoshiro Chuman, Lihong Shi, Takuya Masuda, Thomas Wyttenbach, Michael T. Bowers, Kohei Uosaki, Kazuyasu Sakaguchi

    Advanced Functional Materials   23 ( 39 )   4881 - 4887   2013.10

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    DOI: 10.1002/adfm.201300577

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  • Effects of E/Z Configuration of Fluoroalkene-containing HDAC Inhibitors on Selectivity for HDAC Isoforms Reviewed

    Yoshiro Chuman, Mariko Ueyama, Satoshi Sano, Fei Wu, Yuhei Kiyota, Takayoshi Higashi, Satoshi Osada, Kazuyasu Sakaguchi

    CHEMISTRY LETTERS   42 ( 8 )   833 - 835   2013.8

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    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1246/cl.130243

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  • Inhibition of tumor suppressor protein p53-dependent transcription by a tetramerization domain peptide via hetero-oligomerization Reviewed

    Junya Wada, Rui Kamada, Toshiaki Imagawa, Yoshiro Chuman, Kazuyasu Sakaguchi

    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS   22 ( 8 )   2780 - 2783   2012.4

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    DOI: 10.1016/j.bmcl.2012.02.085

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  • A small molecule inhibitor of p53-inducible protein phosphatase PPM1D Reviewed

    Hiroaki Yagi, Yoshiro Chuman, Yuuki Kozakai, Toshiaki Imagawa, Yu Takahashi, Fumihiko Yoshimura, Keiji Tanino, Kazuyasu Sakaguchi

    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS   22 ( 1 )   729 - 732   2012.1

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    DOI: 10.1016/j.bmcl.2011.10.084

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  • Phosphatase assay for multi-phosphorylated substrates using phosphatase specific-motif antibody Reviewed

    Yoshiro Chuman, Kanako Iizuka, Takeshi Honda, Hitoshi Onoue, Yasuyuki Shimohigashi, Kazuyasu Sakaguchi

    JOURNAL OF BIOCHEMISTRY   150 ( 3 )   319 - 325   2011.9

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    DOI: 10.1093/jb/mvr056

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  • Probing Phenylalanine Environments in Oligomeric Structures with Pentafluorophenylalanine and Cyclohexylalanine Reviewed

    Takao Nomura, Rui Kamada, Issaku Ito, Koichi Sakamoto, Yoshiro Chuman, Koichiro Ishimori, Yasuyuki Shimohigashi, Kazuyasu Sakaguchi

    BIOPOLYMERS   95 ( 6 )   410 - 419   2011.6

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    DOI: 10.1002/bip.21594

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  • sFRP-1 binds via its netrin-related motif to the N-module of thrombospondin-1 and blocks thrombospondin-1 stimulation of MDA-MB-231 breast carcinoma cell adhesion and migration Reviewed

    Gema Martin-Manso, Maria J. Calzada, Yoshiro Chuman, John M. Sipes, Charles P. Xavier, Vladimir Wolf, Svetlana A. Kuznetsova, Jeffrey S. Rubin, David D. Roberts

    ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS   509 ( 2 )   147 - 156   2011.5

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    DOI: 10.1016/j.abb.2011.03.004

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  • Effective method for formation of functionalized nanowires using amyloid peptides Reviewed

    Sakai Hiroki, Watanabe Ken, Chuman Yoshiro, Uosaki Kohei, Sakaguchi Kazuyasu

    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY   241   2011.3

  • Novel chemical inhibitors specific for p53-inducible protein phosphatase PPM1D Reviewed

    Yagi Hiroaki, Chuman Yoshiro, Yoshimura Fumihiko, Tanino Keiji, Sakaguchi Kazuyasu

    Abstracts of Papers of the American Chemical Society   241   2011

  • Enhancement of transcriptional activity of mutant p53 tumor suppressor protein through stabilization of tetramer formation by calix[6]arene derivatives Reviewed

    Rui Kamada, Wataru Yoshino, Takao Nomura, Yoshiro Chuman, Toshiaki Imagawa, Takanori Suzuki, Kazuyasu Sakaguchi

    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS   20 ( 15 )   4412 - 4415   2010.8

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    DOI: 10.1016/j.bmcl.2010.06.053

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  • Drastic Effects on Fibril Formation of Amyloid-beta Peptides by the Addition of Amino Acid Residue Units to the Termini Reviewed

    Yuya Asanomi, Yumiko Kobayashi, Hiroki Sakai, Takuya Masuda, Xinjiang Chen, Yoshiro Chuman, Kohei Uosaki, Kazuyasu Sakaguchi

    PROTEIN AND PEPTIDE LETTERS   17 ( 4 )   458 - 463   2010.4

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    DOI: 10.2174/092986610790963618

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  • Fluoroalkene modification of mercaptoacetamide-based histone deacetylase inhibitors Reviewed

    Satoshi Osada, Satoshi Sano, Mariko Ueyama, Yoshiro Chuman, Hiroaki Kodama, Kazuyasu Sakaguchi

    BIOORGANIC & MEDICINAL CHEMISTRY   18 ( 2 )   605 - 611   2010.1

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    DOI: 10.1016/j.bmc.2009.12.005

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  • Oxidation of Methionine Residue at Hydrophobic Core Destabilizes p53 Tetrameric Structure Reviewed

    Takao Nomura, Rui Kamada, Issaku Ito, Yoshiro Chuman, Yasuyuki Shimohigashi, Kazuyasu Sakaguchi

    BIOPOLYMERS   91 ( 1 )   78 - 84   2009.1

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    DOI: 10.1002/bip.21084

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  • PPM1D430, a Novel Alternative Splicing Variant of the Human PPM1D, can Dephosphorylate p53 and Exhibits Specific Tissue Expression Reviewed

    Yoshiro Chuman, Wataru Kurihashi, Yohei Mizukami, Takehiro Nashimoto, Hiroaki Yagi, Kazuyasu Sakaguchi

    JOURNAL OF BIOCHEMISTRY   145 ( 1 )   1 - 12   2009.1

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    DOI: 10.1093/jb/mvn135

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  • Effects of tumor-associated mutations in the p53 tetramerization domain on oligomerization state and transcriptional activity. Reviewed

    Kamada, R, Terai, T, Nomura, T, Chuman, Y, Imagawa, T, Sakaguchi, K

    Adv. Exp. Med. Biol.   611   567 - 568   2009

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    DOI: 10.1007/978-0-387-73657-0_249

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  • Characterization of the active site and a unique uncompetitive inhibitor of the PPM1-type protein phosphatase PPM1D Reviewed

    Yoshiro Chuman, Hiroaki Yagi, Tomohiko Fukuda, Takao Nomura, Miho Matsukizono, Yasuyuki Shimohigashi, Kazuyasu Sakaguchi

    PROTEIN AND PEPTIDE LETTERS   15 ( 9 )   938 - 948   2008.9

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    DOI: 10.2174/092986608785849236

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  • Differential recognition of phosphorylated transactivation domains of p53 by different p300 domains Reviewed

    Smarajit Polley, Soumi Guha, Neeladri Sekhar Roy, Sanchari Kar, Kazuyasu Sakaguchi, Yoshiro Chuman, V. Swaminathan, Tapas Kundu, Siddhartha Roy

    JOURNAL OF MOLECULAR BIOLOGY   376 ( 1 )   8 - 12   2008.2

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    DOI: 10.1016/j.jmb.2007.11.082

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  • Differential receptor binding characteristics of consecutive phenylalanines in mu-opioid specific peptide ligand endomorphin-2 Reviewed

    Takeshi Honda, Naoto Shirasu, Kaname Isozaki, Michiaki Kawano, Daiki Shigehiro, Yoshiro Chuman, Tsugumi Fujita, Takeru Nose, Yasuyuki Shimohigashi

    BIOORGANIC & MEDICINAL CHEMISTRY   15 ( 11 )   3883 - 3888   2007.6

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    DOI: 10.1016/j.bmc.2007.03.009

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  • Function of Basic Loop in Substrate Recognition of Protein Phosphatase PPM1D. Reviewed

    Chuman, Y, Fukuda, T, Yagi, H, Sakaguchi, K

    Peptide Sci.   2006   17 - 18   2007

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  • Structural isoforms of the circadian neuropeptide PDF expressed in the optic lobes of the cricket Gryllus bimaculatus: Immunocytochemical evidence from specific monoclonal antibodies Reviewed

    Takeshi Honda, Ayami Matsushima, Kazunori Sumida, Yoshiro Chuman, Kazuyasu Sakaguchi, Hitoshi Onoue, Ian A. Meinertzhagen, Yasuyuki Shimohigashi, Miki Shimohigashi

    JOURNAL OF COMPARATIVE NEUROLOGY   499 ( 3 )   404 - 421   2006.11

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    DOI: 10.1002/cne.21112

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  • Different structural requirements for the constitutive and the agonist-induced activities of the beta(2)-adrenergic receptor Reviewed

    C Ambrosio, P Molinari, F Fanelli, Y Chuman, M Sbraccia, O Ugur, T Costa

    JOURNAL OF BIOLOGICAL CHEMISTRY   280 ( 25 )   23464 - 23474   2005.6

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    DOI: 10.1074/jbc.M502901200

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  • Mechanism of Amyloid-Like Fibrillar Aggregation of Mutant Peptide of p53 Tetramerization Domain

    ASANOMI Yuya, TAKAKUSAGI Satoru, CHUMAN Yoshiro, KAYA Shunji, IMAGAWA Toshiaki, UOSAKI Kohei, SAKAGUCHI Kazuyasu

    Peptide Science   2004 ( 0 )   313 - 316   2005.3

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  • Molecular Cloning and Circadian Expression Profile of Pacemaker Neuropeptide PDF in Diptera

    Matsushima, S, Yokotani, S, Sato, S, Kaneki, A, Takeda, Y, Chuman, Y, Ozaki, M, Asai, D, Nose, T, Onoue, H, Ito, Y, Tominaga, Y, Shimohigashi, Y, Shimohigashi, M

    Lett., Peptide Sci.   2005

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  • Identification of a peptide binding motif for secreted frizzled-related protein-1 Reviewed

    Y Chuman, A Uren, J Cahill, C Regan, Wolf, V, BK Kay, JS Rubin

    PEPTIDES   25 ( 11 )   1831 - 1838   2004.11

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    DOI: 10.1016/j.peptides.2004.07.010

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  • Secreted frizzled-related protein-1 inhibits RANKL-dependent osteoclast formation Reviewed

    KD Hausler, NJ Horwood, Y Chuman, JL Fisher, J Ellis, TJ Martin, JS Rubin, MT Gillespie

    JOURNAL OF BONE AND MINERAL RESEARCH   19 ( 11 )   1873 - 1881   2004.11

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    DOI: 10.1359/JBMR.040807

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  • Structural analysis and identification of novel isoforms of the circadian clock gene period in the silk moth Bombyx mori Reviewed

    Y Takeda, Y Chuman, N Shirasu, S Sato, A Matsushima, A Kaneki, Y Tominaga, Y Shimohigashi, M Shimohigashi

    ZOOLOGICAL SCIENCE   21 ( 9 )   903 - 915   2004.9

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    DOI: 10.2108/zsj.21.903

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  • cDNA cloning of the housefly pigment-dispersing factor (PDF) precursor protein and its peptide comparison among the insect circadian neuropeptides Reviewed

    A Matsushima, S Sato, Y Chuman, Y Takedo, S Yokotani, T Nose, Y Tominaga, M Shimohigashi, Y Shimohigashi

    JOURNAL OF PEPTIDE SCIENCE   10 ( 2 )   82 - 91   2004.2

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    DOI: 10.1002/psc.511

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  • Molecular cloning and circadian expression profile of insect neuropeptide PDF in black blowfly, Phormia regina. Reviewed

    Matsushima, A, Yokotani, S, Liu, X, Sumida, K, Honda, T, Sato, S, Kaneki, A, Takeda, Y, Chuman, Y, Ozaki, M, Asai, D, Nose, T, Onoue, H, Ito, Y, Tominaga, Y, Shimohigashi, Y, Shimohigashi, M

    Lett. Peptide Sci.   10   419 - 430   2003

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    DOI: 10.1007/BF02442573

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  • A circadian neuropeptide, pigment-dispersing Factor-PDF, in the last-summer cicada Meimuna opalifera: cDNA cloning and immunocytochemistry Reviewed

    S Sato, Y Chuman, A Matsushima, Y Tominaga, Y Shimohigashi, M Shimohigashi

    ZOOLOGICAL SCIENCE   19 ( 8 )   821 - 828   2002.8

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    DOI: 10.2108/zsj.19.821

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  • cDNA cloning and nuclear localization of the cireadian neuropeptide designated as pigment-dispersing factor PDF in the cricket Gryllus bimaculatus Reviewed

    Y Chuman, A Matsushima, S Sato, K Tomioka, Y Tominaga, IA Meinertzhagen, Y Shimohigashi, M Shimohigashi

    JOURNAL OF BIOCHEMISTRY   131 ( 6 )   895 - 903   2002.6

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    DOI: 10.1093/oxfordjournals.jbchem.a003180

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  • The role of deltorphin II phenylalanine reside in binding to the delta opioid receptor Reviewed

    T Honda, N Shirasu, Y Chuman, K Okada, T Fujita, T Nose, Y Shimohigashi

    BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN   73 ( 11 )   2549 - 2552   2000.11

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    DOI: 10.1246/bcsj.73.2549

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  • Highly potent nociceptin analog containing the Arg-Lys triple repeat Reviewed

    K Okada, T Sujaku, Y Chuman, R Nakashima, T Nose, T Costa, Y Yamada, M Yokoyama, A Nagahisa, Y Shimohigashi

    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS   278 ( 2 )   493 - 498   2000.11

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    DOI: 10.1006/bbrc.2000.3822

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  • Regional and accelerated molecular evolution in group I snake venom gland phospholipase A(2) isozymes Reviewed

    Y Chuman, Nobuhisa, I, T Ogawa, M Deshimaru, T Chijiwa, NH Tan, Y Fukumaki, Y Shimohigashi, F Ducancel, JC Boulain, A Menez, M Ohno

    TOXICON   38 ( 3 )   449 - 462   2000.3

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    DOI: 10.1016/S0041-0101(99)00165-8

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  • Napsin A, a member of the aspartic protease family, is abundantly expressed in normal lung and kidney tissue and is expressed in lung adenocarcinomas Reviewed

    Y Chuman, AC Bergman, T Ueno, S Saito, K Sakaguchi, AA Alaiya, B Franzen, T Bergman, D Arnott, G Auer, E Appella, H Jornvall, S Linder

    FEBS LETTERS   462 ( 1-2 )   129 - 134   1999.11

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    DOI: 10.1016/S0014-5793(99)01493-3

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  • Exploration of universal cysteines in the binding sites of three opioid receptor subtypes by disulfide-bonding affinity labeling with chemically activated thiol-containing dynorphin A analogs Reviewed

    Naoto Shirasu, Takuya Kuromizu, Hidenori Nakao, Yoshiro Chuman, Takeru Nose, Tommaso Costa, Yasuyuki Shimohigashi

    Journal of Biochemistry   126 ( 1 )   254 - 259   1999.1

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    DOI: 10.1093/oxfordjournals.jbchem.a022430

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  • A novel type of rat brain delta opioid receptors differenciated by cyclopropylphenyl alanine-containing enkephalin analog Reviewed

    Y Chuman, T Yasunaga, T Costa, Y Shimohigashi

    PEPTIDE SCIENCE - PRESENT AND FUTURE   207 - 209   1999

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  • Exploration of universal cysteines in the binding sites of three opioid receptor subtypes by disulfide-bonding affinity labeling with chemically activated thiol-containing dynorphin A analogs. Reviewed

    Shirasu, N, Kuromizu. T, Nakao, H, Chuman, Y, Nose, T, Costa, T, Shimohigashi, Y

    J. Biochem.   126   254 - 259   1999

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  • Retrotransposable CR1-like elements in crotalinae snake genomes Reviewed

    Nobuhisa, I, T Ogawa, M Deshimaru, T Chijiwa, K Nakashima, Y Chuman, Y Shimohigashi, Y Fukumaki, S Hattori, M Ohno

    TOXICON   36 ( 6 )   915 - 920   1998.6

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    DOI: 10.1016/S0041-0101(97)00104-9

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  • Discrimination of a novel type of rat brain delta opioid receptors by enkephalin analog containing structurally constrained cyclopropylpheynlanine (del Phe) Reviewed

    Y Chuman, T Yasunaga, T Costa, Y Shimohigashi

    BIOCHEMISTRY AND MOLECULAR BIOLOGY INTERNATIONAL   42 ( 6 )   1227 - 1233   1997.9

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Books

  • 光刺激応答性核酸の現状と新規核酸創薬モダリティへの応用

    山形 優香, 鈴木 未来, 水沼 正昂, 中馬 吉郎( Role: Joint author)

    Precision Medicine  2022.11 

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  • Trends and development of stimuli-responsive oligonucleotide drugs in spatiotemporally controlled manner

    Yuka Yamagata, Mirai Suzuki, Masataka Mizunuma, Yoshiro Chuman( Role: Joint author)

    2021.12 

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  • Application of Mn2+-specific Biosensor Based on 2. G-quadruplex DNA Aptamer

    Mizunuma, M, Kaneko, A, Watari, M, Saito, H, Banno, A, Yamagata, Y, Furukawa, K, Chuman, Y(Peptide Sci. 2021, 135-136)

    The Japanese Peptide Society, Peptide Sci. 2021, 135-136  2021.5 

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  • アプタマー創薬の現状と細胞膜 自動透過性DNAアプタマーの開発

    水沼 正昂, 坂野 彰則, 金子 敦巳, 亘 美佑, 中馬 吉郎( Role: Joint author)

    月刊「細胞」  2020.5 

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  • 発がん関連酵素に対するDNAアプタマーを用いた新規阻害剤開発と応用

    月刊「細胞」  2019.2 

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  • 核酸アプタマーを用いた発がん関連酵素に対する新規阻害剤開発と応用

    アグリバイオ  2018.12 

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  • 発がん関連Ser/Thrホスファターゼに対する新規阻害剤と基質同定法の開発

    ( Role: Joint author)

    Bio Clinica  2018.5 

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  • 発がん関連Ser/Thrホスファターゼに対する新規阻害剤の開発

    ( Role: Joint author)

    Bio Clinica  2017.12 

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  • がん原遺伝子産物PPM1Dの細胞がん化機構および創薬を指向した阻害剤

    生化学/日本生化学会  2015 

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  • アミノ酸リシンに新たな翻訳後修飾

    化学/化学同人  2011 

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  • 鎮痛および疼痛にかかわる神経ペプチド

    医学のあゆみ/医歯薬出版株式会社  2000 

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Presentations

  • 細胞内を標的可能な新規創薬プラットホーム:IRDAptamer Invited

    中馬 吉郎

    第2回 BVA バイオインターフェース  2022.3 

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    Event date: 2022.3

    Presentation type:Oral presentation (general)  

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  • 細胞内標的を認識可能な新規創薬モダリティの開発

    中馬吉郎

    TGA DemoDay  2022.3 

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    Event date: 2022.3

    Presentation type:Symposium, workshop panel (nominated)  

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  • 細胞内標的を認識可能な新規創薬モダリティの開発

    中馬 吉郎

    みちのくGAPファンド DemoDay  2022.2 

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    Event date: 2022.2

    Presentation type:Symposium, workshop panel (nominated)  

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  • 抗体模倣分子Adnectinを用いた発がん関連ホスファターゼScp1阻害剤の開発

    中馬吉郎

    第10回日本プロテインホスファターゼ研究会 学術集会  2022.1 

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    Event date: 2022.1

    Presentation type:Oral presentation (general)  

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  • Development of Ion-Responsive DNA Aptamer (IRDAptamer) against Oncogenic Protein Phosphatase PPM1D

    Yoshiro Chuman

    自然科学研究機構サイトビジット2021  2021.12 

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    Event date: 2021.12

    Presentation type:Oral presentation (general)  

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  • Ion-responsive DNA Aptamer (IRDAptamer) drugs targeting intercellular oncogenic protein phosphatase PPM1D

    Yoshiro Chuman

    日本核酸医薬学会 第6回年会  2021.6 

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    Event date: 2021.6

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  • 細胞内を標的可能な新規創薬プラットホームの開発, 刺激応答性DNAアプタマー: IRDAptamer

    中馬 吉郎

    BioJapan2024  2024.10 

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  • DNA四重鎖G4構造を母体とした新規機能性ツール:IRDAptamerの開発と応用 Invited

    中馬 吉郎

    第5回アプタマー研究会  2024.3 

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  • Development of Scp1 protein phosphatase inhibitors from new drug platform IRDAptamer library

    Yoshiro Chuman

    The 5th Japan-Taiwan Bilateral Conference on Protein Phosphatase  2024.3 

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  • New drug modality: IRDAptamers Invited

    Yoshiro Chuman

    Biological Chemistry Symposium 2023  2023.9 

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  • 細胞内を標的可能な新規創薬プラットホームの開発 刺激応答性DNAアプタマー: IRDAptamer

    中馬 吉郎

    エッセンスフォーラム2023  2023.9 

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  • 多様な疾患に適応可能なキューブ型DNAアプタマー IRDAptamer Invited

    中馬吉郎

    2023年度 第1回BVA定例会  2023.7 

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  • Development of Adnectins Targeting the Oncogenic Ser/Thr Protein Phosphatase PPM1D Invited

    Yoshiro Chuman

    2023.5 

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  • 新規創薬モダリティ:IRDAptamerの開発と応用 Invited

    中馬吉郎

    医療・診断の化学シンポジウム  2023.3 

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  • 細胞内を標的可能な新規創薬プラットホームの開発 Invited

    みちのくGAPファンド DemoDay  2023.2 

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  • DEVELOPMENT OF MEMBRANE-PERMEABLE DNA APTAMERS TARGETING ONCOGENIC SER/THR PROTEIN PHOSPHATASE PPM1D Invited

    Yoshiro Chuman

    2022.12 

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  • 細胞内を標的可能な新規創薬モダリティ:IRDAptamerの開発 Invited

    第4回 BVAバイオインターフェース  2022.11 

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  • 膜透過性DNA アプタマー: IRDAptamer を用いた創薬モダリティの開発 Invited

    中馬吉郎

    第95回 日本生化学会  2022.11 

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  • 細胞内を標的可能な新規創薬モダリティの開発 Invited

    中馬吉郎

    第3回BVA創薬研究会  2022.9 

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  • Identification of the Binding Molecules for Disease-related Proteins using Adn-based Phage Display Libraries

    Yoshiro CHUMAN

    The 18th AKABORI Conference 2020  2021.3 

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  • Specific Inhibitors for Oncogenic Protein Phosphatase PPM1D Using G-quadruplex-based DNA aptamer library Invited

    Yoshiro CHUMAN

    14th International Conference on Protein Phosphatases  2020.12 

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  • Development of Cell Penetrating DNA aptamers for Oncogenic Protein Phosphatase PPM1D Invited

    Yoshiro CHUMAN

    The 43th Annual Meeting of the Molecular Biology Society of Japan  2020.12 

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  • 刺激応答性DNAアプタマー(IRDAptamer)を用いた疾患関連ホスファターゼ阻害剤の開発 Invited

    中馬 吉郎

    第93回日本生化学会大会  2020.9 

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  • Identification of Specific Inhibitors for Oncogenic Protein Phosphatase PPM1D Using Ion-responsive DNA Aptamer (IRDAptamer) Library Invited

    Yoshiro CHUMAN

    The 42th Annual Meeting of the Molecular Biology Society of Japan  2019.12 

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  • Construction of Structurally-Controlled Platform for Identification of Specific Inhibitors against Oncogenic Ser/Thr Protein Phosphatases Invited

    Yoshiro CHUMAN

    2019 Taiwan-Japan Bilateral Conference on Phosphatase (4th)  2019.11 

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  • Development of Ion-responsive DNA Aptamer (IRDAptamer) Drugs Targeting Intracellular Oncogenic Proteins

    Yoshiro CHUMAN

    2019.10 

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  • リン酸化ミミック分子を用いたSer/Thrホスファターゼ活性中心結合分子の開発

    中馬 吉郎

    第9回日本プロテインホスファターゼ研究会  2019.7 

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  • 抗体模倣分子を用いた機能性分子の開発とポスト抗体薬への展開

    中馬 吉郎

    第6回U-goサロン  2019.6 

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  • 『化学』の視点から生命現象を理解する:総合大学の利点を生かした分野横断型融合研究の展開 Invited

    中馬 吉郎

    自然系研究最前線セミナー  2019.3 

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  • イオン応答性DNAアプタマー(IRDAptamer)を用いたPPM1D阻害剤の開発 Invited

    中馬 吉郎

    生物化学研究会2018  2019.3 

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  • Specific Inhibitors for Oncogenic PPM1D Phosphatase Using ion-responsive DNA aptamer (IRDAptamer) Invited International conference

    CHUMAN Yoshiro

    The 13th International Conference on Protein Phosphatase  2018.10 

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    Venue:Tokyo  

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  • Substrate identification method for protein phosphatases using phosphorylation mimic phage display Invited International conference

    CHUMAN Yoshiro

    AKABORI Conference 2018  2018.9 

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    Venue:Lindau (Germany)  

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  • 発がん関連脱リン酸化酵素を標的とした阻害剤と新規基質同定法の開発 Invited

    CHUMAN Yoshiro

    N-Hybrid conference 2018  2018.1 

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    Venue:Niigata  

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  • Development of Specific Inhibitors for Oncogenic PPM1D Phosphatase Using Rigid-scaffold Structural Libraries

    CHUMAN Yoshiro

    The 3rd Japan-Taiwan Bilateral Conference on Protein Phosphatase  2017.11 

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    Venue:Sendai  

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  • 発がんタンパク質PPM1Dを標的とした刺激応答性アプタマー阻害剤の開発 Invited

    CHUMAN Yoshiro

    第3回アプタマー研究会  2017.3 

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    Venue:Kurume  

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  • Screening of binding molecules for Ser/Thr phosphatases from rigid structural libraries International conference

    CHUMAN Yoshiro

    The 12th International Conference on Protein Phosphatase  2016.10 

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    Venue:Osaka  

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  • 酵素-基質複合体誘導によるSer/Thrホスファターゼ基質同定法の開発と応用 Invited

    CHUMAN Yoshiro

    第89回日本生化学会  2016.9 

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    Venue:Sendai  

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  • 立体制約型libraryを用いた疾患関連タンパク質結合分子の同定 Invited

    CHUMAN Yoshiro

    フォーラム「生命科学談話シリーズ」  2016.4 

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    Venue:Fukuoka  

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  • 発癌関連ホスファターゼに対する新規基質同定法と阻害剤の開発 Invited

    CHUMAN Yoshiro

    第22回ペプチドフォーラム  2016.3 

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    Venue:Kanazawa  

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  • PPM1Dホスファターゼ過剰発現による新規発癌機構 Invited

    CHUMAN Yoshiro

    第46 回 若手ペプチド夏の勉強会  2014.8 

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    Venue:Kyoto  

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  • ヒトPPM1Dホスファターゼによる染色体不安定化と新規発がん機構 Invited

    CHUMAN Yoshiro

    第55回新潟生化学懇話会  2014.6 

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    Venue:Nakaoka  

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  • 翻訳後修飾酵素の制御異常による発がん機構と抗がん剤の開発 Invited

    CHUMAN Yoshiro

    グリーンケミストリー第4回研究シンポジウム  2014.3 

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    Venue:Niigata  

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  • Genome Instability in the Cells Overexpressing p53-inducible Protein Phosphatase PPM1D Invited International conference

    CHUMAN Yoshiro

    2nd Taiwan-Japan Bilateral Conference on Protein Phosphatases  2013.12 

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    Venue:Taiwan  

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  • p53誘導性ホスファターゼPPM1D研究の新展開

    CHUMAN Yoshiro

    生物化学研究会2013  2013.9 

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    Venue:Sapporo  

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  • p53誘導性ホスファターゼPPM1D過剰発現による染色体不安定性機構

    CHUMAN Yoshiro

    第86回日本生化学会  2013.9 

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    Venue:Yokohama  

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  • 17q23にコードされたPPM1Dホスファターゼ過剰発現による染色体不安定化

    CHUMAN Yoshiro

    第50回 日本生化学会北海道支部会  2013.7 

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    Venue:Sapporo  

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  • Suppression of Breast Cancer Cells Proliferation by a small molecule inhibitor of p53-inducible protein phosphatase PPM1D

    CHUMAN Yoshiro

    5th GCOE international symposium  2012.2 

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    Language:English  

    Venue:Sapporo  

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  • ヒトPPM1ホスファターゼファミリーにおけるリン酸化アミノ酸および金属イオン指向性

    CHUMAN Yoshiro

    第5回 日本プロテインホスファターゼ研究会学術集会  2012.1 

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    Venue:Osaka  

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Industrial property rights

  • 膜透過型核酸アプタマー

    中馬 吉郎, 金子 敦巳, 亘 美佑

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    Application no:特願PCT/JP2020/20119  Date applied:2020.5

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  • 核酸アプタマー

    中馬 吉郎, 金子 敦巳, 亘 美佑

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    Application no:特願2019-096035  Date applied:2019.5

    Patent/Registration no:特許第7477886号  Date registered:2024.4 

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  • 核酸アプタマー及びその使用

    中馬 吉郎, 金子 敦巳, 亘 美佑

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    Application no:特願2019-045938  Date applied:2019.3

    Patent/Registration no:特許第7255852号  Date registered:2023.4 

    Rights holder:新潟大学

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  • Monoclonal antibody specifically recognizing modification site after translation of p53 and kit for assaying modification site containing the same

    Kazuyasu Sakaguchi, Yoshiro Chuman, Yasuo Akebiyama, Miho Matsukizono, Maki Watanabe, Junichi Tsutumi

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    Application no:特願11/910,313  Date applied:2006.3

    Date issued:2011.11

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  • p53翻訳後修飾部位を特異的に認識するモノクローナル抗体、及びその抗体を含む修飾部位測定キット

    坂口 和靖, 中馬 吉郎, 明日山 康生, 松木園 美穂

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    Application no:特願2007-511193, PCT/JP2006/306921 

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  • プロテインホスファターゼ阻害剤

    坂口 和靖, 谷野 圭持, 中馬 吉郎, 吉村 文彦, 八木 寛陽

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    Application no:特願2008-262646, PCT出願PCT/JP2009/005128 

    Publication no:WO2010041401 A1 

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Awards

  • 2010年度(第18回) JB論文賞

    2010  

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    Country:Japan

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  • Fellows Award for Research Excellence (FARE) 2003(National Institutes of Health)

    2002  

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Research Projects

  • 標的細胞へのホーミング能を有するハイブリッド型膜透過性アプタマーの開発

    Grant number:25K22914

    2025.6 - 2028.3

    System name:科学研究費助成事業

    Research category:挑戦的研究(萌芽)

    Awarding organization:日本学術振興会

    中馬 吉郎

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    Grant amount:\6370000 ( Direct Cost: \4900000 、 Indirect Cost:\1470000 )

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  • 転移性肺がんを標的としたDDS機能を内包する細胞膜透過型ポスト抗体薬の開発

    2024.4 - 2025.3

    System name:AMED 「異分野融合型研究シーズ」

    Awarding organization:国立研究開発法人日本医療研究開発機構

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  • パレコウイルスA3感染症の克服に必要な基盤研究技術の創出

    2024.4 - 2025.3

    System name:「新興・再興感染症に対する革新的医薬品等開発推進研究事業」

    Awarding organization:国立研究開発法人日本医療研究開発機構 AMED

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    Authorship:Coinvestigator(s) 

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  • 細胞内を標的可能な新規創薬プラットホームの開発

    2022.9 - 2023.3

    System name:大学発新産業創出プログラム(START)

    Awarding organization:JST

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    Authorship:Principal investigator 

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  • ナノバブル化ネオマクロライドを用いたワクチン副反応の予防薬の開発研究

    Grant number:22K19614

    2022.6 - 2024.3

    System name:科学研究費助成事業 挑戦的研究(萌芽)

    Research category:挑戦的研究(萌芽)

    Awarding organization:日本学術振興会

    寺尾 豊, 中馬 吉郎, 牛田 晃臣, 土門 久哲, 前川 知樹

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    Grant amount:\6500000 ( Direct Cost: \5000000 、 Indirect Cost:\1500000 )

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  • Functional optimization and establishment of comprehensive evaluation of membrane-permeable aptamers for drug development using AI technology

    Grant number:22H02917

    2022.4 - 2025.3

    System name:Grants-in-Aid for Scientific Research Grant-in-Aid for Scientific Research (B)

    Research category:Grant-in-Aid for Scientific Research (B)

    Awarding organization:Japan Society for the Promotion of Science

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    Authorship:Principal investigator 

    Grant amount:\17550000 ( Direct Cost: \13500000 、 Indirect Cost:\4050000 )

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  • 細胞内標的を認識可能な新規創薬モダリティの開発

    2021.9 - 2022.3

    System name:社会還元加速プログラム(SCORE)

    Awarding organization:JST

    代表,中馬 吉郎

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  • 新型コロナウイルスを標的としたキューブ型DNAアプタマー治療薬・検査薬の開発

    2020.9 - 2021.3

    System name:U-go グラント

    Awarding organization:新潟大学

    代表,中馬 吉郎

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  • Development of Next-Generation Platform for Light-induced Drugs

    Grant number:20K21541

    2020.7 - 2023.3

    System name:Grants-in-Aid for Scientific Research Challenging Research (Exploratory)

    Research category:Challenging Research (Exploratory)

    Awarding organization:Japan Society for the Promotion of Science

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    Grant amount:\6370000 ( Direct Cost: \4900000 、 Indirect Cost:\1470000 )

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  • 薬剤耐性肺炎球菌のin vivo MS解析とキューブ型DNA抗菌薬の開発研究

    Grant number:20H03858

    2020.4 - 2024.3

    System name:科学研究費助成事業 基盤研究(B)

    Research category:基盤研究(B)

    Awarding organization:日本学術振興会

    新潟大学, 医歯学系, 寺尾 豊

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    Grant amount:\17940000 ( Direct Cost: \13800000 、 Indirect Cost:\4140000 )

    誤嚥性肺炎に代表される肺炎は,薬剤耐性菌の増加により重症化している.日本政府・WHO等は,耐性菌による肺炎の制御を人類の最重要課題と定めている.申請者は,若手Aから発展させた5回の基盤Bで,好中球と病原細菌のせめぎ合いを独自に解析してきた.その結果,肺炎球菌だけが自己溶菌する細菌であり,溶菌で漏出する細菌分子を活用して免疫系を無力化し,組織傷害を果たすというin vitroでの知見を得た.本研究では,未だ詳細不明なin vivoにおける耐性肺炎球菌による肺炎の重症化機構を解析し,耐性菌による肺炎の治療基盤を構築する.具体的には,耐性肺炎球菌の肺感染マウス系を確立後,肺胞中の耐性菌とマウスの両分子群をiTRAQ-MS/MS法で網羅同定した後,耐性菌とマウスの両分子群の動態を多分子同時解析装置で詳細分析する.そして,肺炎の重症化に関与する分子を治療標的として選出し,萌芽研究のin vitro系で確立し,特許出願したDNA立体化技術を用い,in vivo系において耐性肺炎球菌の病原因子のみを特異的に制御する抗菌薬の開発を期す.
    今年度は,耐性肺炎球菌の病原分子候補の網羅解析に注力した.すなわち,耐性菌の病原分子候補の組換えタンパクを現有機器のLuminex装置にて,多分子同時相互作用解析した.病原分子候補を96ウェルプレートに分注し,それぞれに好中球および肺胞上皮細胞株を添加した.続いて,Luminex装置にて,同一条件下でサイトカインおよび傷害され漏出するミトコンドリア等の内在タンパク質を同時定量し,有意なマウスのin vivo感染マーカーを決定を試みた.さらに,現有設備のBiacoreにて分子間相互作用解析およびWestern blot解析やELISA解析を行い,マウス組織に結合および分解する耐性肺炎球菌の病原分子群を選出した.

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  • 細胞膜自動透過性DNAアプタマーの分子基盤解明とポスト抗体医薬への展開

    2019 - 2021

    System name:基盤研究(B)

    Awarding organization:日本学術振興会

    代表,中馬 吉郎

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    Authorship:Principal investigator  Grant type:Competitive

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  • 「生化学」と「分子進化工学」の融合的プロテオミクスによる,神経軸索形成・再生のための脂質ラフとを介したタンパク質間相互作用の網羅的解析

    2018.9 - 2019.3

    System name:U-goグラント

    Awarding organization:新潟大学

    新潟大学,医歯学系,本多敦子

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  • 外部刺激応答性DNAアプタマーの抗がん剤展開と発がんタンパク質結晶化への応用

    2018 - 2020

    System name:特別研究員奨励費(DC1)

    Awarding organization:日本学術振興会

    新潟大学,自然科学系,金子 敦巳

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    Grant type:Competitive

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  • MRSA特異的な3D転換性DNAアプタマー型抗菌薬の構築と開発技術の確立研究

    2018 - 2019

    System name:挑戦的研究(萌芽)

    Awarding organization:日本学術振興会

    新潟大学, 医歯学系, 寺尾 豊

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    Grant type:Competitive

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  • 細胞内疾患原因タンパク質を標的とした自動ホーミング分子の開発

    2018 - 2019

    System name:U-go グラント

    Awarding organization:新潟大学

    代表,中馬 吉郎

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    Authorship:Principal investigator  Grant type:Competitive

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  • 刺激応答性機能分子IRDAptamerを用いた細胞内制御可能な抗がん剤開発

    2017 - 2018

    System name:U-go グラント

    Awarding organization:新潟大学

    代表,中馬 吉郎

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    Authorship:Principal investigator  Grant type:Competitive

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  • 酵素-基質複合体誘導によるSer/Thrホスファターゼ基質同定法の開発

    2015 - 2017

    System name:基盤研究(C)

    Awarding organization:日本学術振興会

    代表,中馬 吉郎

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    Authorship:Principal investigator  Grant type:Competitive

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  • 癌抑制タンパク質p53の多量体化と配向化を基盤とした生物イベント制御と機能解明

    2012 - 2015

    System name:基盤研究(B)

    Awarding organization:日本学術振興会

    北海道大学,理学(系, 研究科, 究院),坂口 和靖

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    Grant type:Competitive

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  • PPM1Dホスファターゼ過剰発現細胞における染色体分配制御の破綻と分子基盤解明

    2012 - 2014

    System name:基盤研究(C)

    Awarding organization:日本学術振興会

    代表,中馬 吉郎

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    Authorship:Principal investigator  Grant type:Competitive

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  • p53四量体ドメインおよびエラスチンペプチドを用いた温度可変型機能性タンパク質の創出

    2011 - 2012

    System name:GCOEプログラム若手研究者研究活動経費

    Awarding organization:日本学術振興会

    代表,中馬 吉郎

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    Authorship:Principal investigator  Grant type:Competitive

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  • 温度制御分子デバイスを用いた発がんタンパク質PPM1D阻害剤のスクリーニング

    2010 - 2011

    System name:GCOEプログラム若手研究者研究活動経費

    Awarding organization:日本学術振興会

    代表,中馬 吉郎

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    Authorship:Principal investigator  Grant type:Competitive

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  • p53-inducible protein phosphatase PPM1D: Substrate recognition and its novel Inhibitors

    2009.9 - 2010.3

    System name:グローバルCOE 若手教員海外ネットワーク形成支援事業

    Awarding organization:日本学術振興会

    代表,中馬 吉郎

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  • Stability Change of Tetrameric Structure of Tumor Suppressor Protein p53 in Mutation and Evolution, and Threshold for Loss of Tumor Suppressor Activity in Terms of Disruption of the Tetrameric Structure.

    Grant number:21310133

    2009 - 2012

    System name:Grants-in-Aid for Scientific Research

    Research category:Grant-in-Aid for Scientific Research (B)

    Awarding organization:Japan Society for the Promotion of Science

    SAKAGUCHI Kazuyasu, TOSHIAKI Imagawa, CHUMAN Yoshiro

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    Grant type:Competitive

    The tumor suppressor p53 induces cell cycle arrest and apoptosis in response to genotoxic stress. About 50% of human tumors have TP53 gene mutations ; most are missense ones that presumably lower p53's tumor suppressor activity. In this study, we explored the effects of known tumor-derived missense mutations on the stability and oligomeric structure of p53. The results suggested that threshold for loss of tumor suppressor activity in terms of the disruption of p53's tetrameric structure could be extremely low. We developed a calixarene derivative that could increase the tetrameric stability of the mutant R337H, which is found in Li-Fraumeni syndrome, a hereditary disorder characterized by familial clusters of early-onset multiple tumors. We also showed that the tetramer stability increased through the evolution of vertebrates : fish-amphibian-bird and mammals. The results suggested that the folding of the tetramerization domain would tightly control its functional expression.

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  • p53誘導性ホスファターゼPPM1Dの細胞周期における新規制御機構の解明

    2009 - 2010

    System name:GCOEプログラム若手研究者研究活動経費

    Awarding organization:日本学術振興会

    代表,中馬 吉郎

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    Authorship:Principal investigator  Grant type:Competitive

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  • p53誘導性ホスファターゼPPM1Dスプライシング多型による発がん機構の解明

    2008 - 2010

    System name:若手研究(B)

    Awarding organization:日本学術振興会

    代表,中馬 吉郎

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    Authorship:Principal investigator  Grant type:Competitive

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  • PPM1D特異的阻害剤による乳がん細胞増殖抑制と制御機構の解明

    2008 - 2009

    System name:GCOEプログラム若手研究者研究活動経費

    Awarding organization:日本学術振興会

    代表,中馬 吉郎

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    Authorship:Principal investigator  Grant type:Competitive

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  • 新規PPM1D阻害剤を用いた抗癌剤併用療法への展開と薬剤作用機構の解明

    2007 - 2008

    System name:GCOEプログラム若手研究者研究活動経費

    Awarding organization:日本学術振興会

    代表,中馬 吉郎

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    Authorship:Principal investigator  Grant type:Competitive

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  • p53四量体ドメインおよびエラスチンペプチドを用いた温度可変型機能性タンパク質の創出

    2007 - 2008

    System name:グローバルCOEプログラム若手研究者研究活動経費

    Awarding organization:日本学術振興会

    代表, 中馬 吉郎

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  • がん抑制タンパク質p53四量体形成変異による不活性化機構の解明と機能修復剤の開発

    2006 - 2008

    System name:基盤研究(B)

    Awarding organization:日本学術振興会

    北海道大学,理学(系, 研究科, 究院),坂口 和靖

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    Grant type:Competitive

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  • p53誘導性ホスファターゼPPM1Dの機能解析用分子ツールとしての阻害剤開発

    2005 - 2007

    System name:若手研究(B)

    Awarding organization:日本学術振興会

    代表,中馬 吉郎

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    Authorship:Principal investigator  Grant type:Competitive

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  • がん抑制タンパク質p53の四量体形成ドメインのフォールディング

    2004 - 2005

    System name:特定領域研究

    Awarding organization:日本学術振興会

    北海道大学,理学(系, 研究科, 究院),坂口 和靖

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    Grant type:Competitive

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  • がん遺伝子治療用の非ヘテロ四量体形成性がん抑制タンパク質p53の設計と開発

    2002 - 2004

    System name:基盤研究(B)

    Awarding organization:日本学術振興会

    北海道大学,理学(系, 研究科, 究院),坂口和靖

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  • エンケファリン内蔵の変異オピオイド受容体による受容体分子機構の解明

    1998 - 2000

    System name:特別研究員奨励費

    Awarding organization:日本学術振興会

    代表,中馬 吉郎

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    Authorship:Principal investigator  Grant type:Competitive

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Teaching Experience

  • 化学特論IV

    2024
    Institution name:新潟大学

  • 化学とSDGs

    2023
    Institution name:新潟大学

  • 先端科学技術総論

    2023
    Institution name:新潟大学

  • 統合化学入門

    2023
    Institution name:新潟大学

  • 化学コロキウム

    2022
    Institution name:新潟大学

  • 生理機能化学

    2022
    Institution name:新潟大学

  • 分子生理化学

    2022
    Institution name:新潟大学

  • 化学特論III

    2021
    Institution name:新潟大学

  • 理学スタディ・スキルズ

    2021
    Institution name:新潟大学

  • 課題研究 a

    2020
    Institution name:新潟大学

  • 課題研究 b

    2020
    Institution name:新潟大学

  • 理学スタディ・スキルズ

    2019
    -
    2021
    Institution name:新潟大学

  • 科学技術英語

    2018
    Institution name:新潟大学

  • コミュニケーション演習

    2018
    Institution name:新潟大学

  • 自然科学基礎実験

    2017
    Institution name:新潟大学

  • 生体分子化学Ⅱ

    2017
    Institution name:新潟大学

  • 化学基礎実習b

    2017
    Institution name:新潟大学

  • 化学基礎実習a

    2017
    Institution name:新潟大学

  • 課題研究

    2017
    -
    2023
    Institution name:新潟大学

  • Advances in Physics and Chemistry

    2017
    Institution name:新潟大学

  • 化学コロキウム

    2017
    Institution name:新潟大学

  • 数理物質科学演習Ⅰ(化学)

    2015
    Institution name:新潟大学

  • 安全教育

    2015
    Institution name:新潟大学

  • 数理物質科学特定研究Ⅰ(化学)

    2015
    Institution name:新潟大学

  • 生化学実験

    2014
    Institution name:新潟大学

  • 生化学演習

    2014
    Institution name:新潟大学

  • 生理機能化学

    2014
    -
    2022
    Institution name:新潟大学

  • グリーンケミストリー入門

    2014
    -
    2022
    Institution name:新潟大学

  • 分子生理化学

    2014
    -
    2022
    Institution name:新潟大学

  • 化学実験

    2014
    -
    2016
    Institution name:新潟大学

  • 課題研究(化学科)

    2014
    -
    2016
    Institution name:新潟大学

  • 生体分子化学II

    2014
    -
    2016
    Institution name:新潟大学

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Social Activities

  • 高大連携 出前講義(科研費アウトリーチ等)

    Role(s): Lecturer

    新潟県立長岡大手高等学校 出前講義  2025.7

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  • 高大連携 出前講義(科研費アウトリーチ等)

    Role(s): Lecturer

    新大x刈羽小学校★サマーセッション  2024.9

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  • 高大連携 出前講義(科研費アウトリーチ等)

    Role(s): Lecturer

    高田北城高校研究室訪問  2024.7

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  • 高大連携 出前講義(科研費アウトリーチ等)

    Role(s): Lecturer

    新潟県立高田高等学校 出前講義  2023.8

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  • 高大連携 出前講義(科研費アウトリーチ等)

    Role(s): Lecturer

    新大×附属長岡中★サマーセッション  2022.9

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