Kawasaki Kiyoshi

カワサキキヨシ | Kawasaki Kiyoshi

Affiliation and department：
Homepage URL (1)： https://research-db.dwc.doshisha.ac.jp/rd/html/japanese/researchersHtml/2791/2791_Researcher.html

Research field (2)： Pharmaceuticals - health and biochemistry , Functional biochemistry

Research theme for competitive and other funds (16)：

2022 - 2026 自然免疫の応答性を調節する抗菌ペプチド等に関する研究
2017 - 2023 内毒素や抗菌ペプチドなどの生物間の攻撃と防御の物質を利用した感染症創薬シーズ研究
2014 - 2018 Creation of a low toxic derivative biosynthesis system for biologically active substances derived from bacteria such as endotoxin
2011 - 2013 Lipopolysaccharide remodeling in bacterial adaptation to host
2008 - 2010 Research for host-recognition and responses against endotoxin modified by pathogenic bacteria.

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Papers (59)：

Saeka Nishihara, Nao Nakamura, Kiyoshi Kawasaki. High amphipathicity of α-helical peptides enhances unmethylated CpG DNA-induced activation of mouse macrophage-like RAW264.7 cells. Scientific Reports. 2024. 14. 1
Waka Sato, Miho Watanabe-Takahashi, Takuya Murata, Naoko Utsunomiya-Tate, Jun Motoyama, Masataka Anzai, Seiko Ishihara, Nanako Nishioka, Hina Uchiyama, Juri Togashi, et al. A tailored tetravalent peptide displays dual functions to inhibit amyloid β production and aggregation. Communications Biology. 2023. 6. 1
Takayuki Ueno, Yumi Yamamoto, Kiyoshi Kawasaki. Phagocytosis of microparticles increases responsiveness of macrophage-like cell lines U937 and THP-1 to bacterial lipopolysaccharide and lipopeptide. Scientific reports. 2021. 11. 1. 6782-6782
Saeka Nishihara, Mayu Wakita, Kiyoshi Kawasaki. Relationship Between Affinity of Kn2-7 to CpG DNA and the Ability of Kn2-7 to Enhance Cellular Uptake of CpG DNA by RAW264.7 Cells. BPB Reports. 2021. 4. 2. 55-58
Daniel J Klionsky, Amal Kamal Abdel-Aziz, Sara Abdelfatah, Mahmoud Abdellatif, Asghar Abdoli, Steffen Abel, Hagai Abeliovich, Marie H Abildgaard, Yakubu Princely Abudu, Abraham Acevedo-Arozena, et al. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1. Autophagy. 2021. 17. 1. 1-382

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MISC (6)：

西原冴佳, 眞鍋貴行, 川崎清史. トレランス状態にあるマクロファージで見られるリポ多糖の積極的取り込みにクラスAスカベンジャー受容体が関与する. 日本薬学会年会要旨集. 2017. 137年会. 3. 137-137
宮下惇嗣, 川崎清史, 関水和久, 垣内力. 無脊椎動物における適応免疫機構. 日本生化学会大会(Web). 2013. 86th
眞鍋貴行, 河野美幸, 川崎清史. サルモネラリポ多糖脱アシル化酵素PagLの活性抑制にはリポ多糖との結合が重要である. 日本生化学会大会・日本分子生物学会年会合同大会講演要旨集. 2010. 83回・33回. 2P-1011
川崎清史, 眞鍋貴行. サルモネラ外膜リパーゼ(PagL)の潜伏性に関わるアミノ酸残基の解析. 脂質生化学研究. 2010. 52. 143-144
眞鍋貴行, 川崎清史. サルモネラ菌のLPS脱アシル化酵素は外膜のアミノアラビノース修飾を認識する. 日本細菌学雑誌. 2008. 63. 1

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Education (2)：

Professional career (1)：

Work history (4)：

2006/04 - 現在 Doshisha Women's College of Liberal Arts Faculty of Pharmaceutical Sciences
1994/04 - 2006/03 国立感染症研究所細胞化学部
2002/07 - 2004/05 (在外)ワシントン大学医学部
1997/11 - 1998/04 (在外)テキサス大学医学部ヒューストン校

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