TAISHU KAWADA

Last Updated :2025/06/04

Affiliations, Positions
Graduate School of Biomedical and Health Sciences(Pharmaceutical Sciences), Assistant Professor
E-mail
kawada-hiroshimahiroshima-u.ac.jp

Basic Information

Major Professional Backgrounds

  • 2024/09/19, 2025/03/31, Tokushima Bunri University, research assistant
  • 2018/04/01, 2020/03/31, Tokushima Bunri University, research assistant

Educational Backgrounds

  • Tokushima Bunri University, 2020/09/19, 2024/09/19
  • Tokushima Bunri University, 2010/04/01, 2016/09/19

Educational Activity

Course in Charge

  1. 2025, Graduate Education (Doctoral Program) , Second Semester, Advanced Research in Pharmaceutical Science

Research Activities

Academic Papers

  1. Increased yields of the guanine oxidative damage product imidazolone following exposure to LED Light, Reactions, 4(4), 801-810, 202312
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  2. N'1,N'4-bis(2-(7,8-dimethyl-2,4-dioxo-3,4-dihydrobenzo[g]pteridin-10(2H)-yl)ethylidene)succinohydrazide., Molbank, M1436, 20220830
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  3. Analysis of nucleotide insertion opposite urea and translesion synthesis across urea by DNA polymerases, Genes Environ, 44(1), 7, 20220215
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  4. Considering existing factors that may cause radiation hormesis at <100 mSv and obey the linear no-threshold theory at ≥100 mSv., Challenges, 12(2), 33, 20211204
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  5. Localizations of the highest occupied molecular orbital and guanine oxidation by UV-light and other oxidizers., Photomed. Photobiol., 42, 1-6, 202103
  6. A strategy for fi nding new medicines against the novel coronavirus disease (COVID-19) derived from base pairing with DNA damages., Infect Dis Clin Res., 6, 60-61, 20201222
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  7. Products of oxidative guanine damage form base pairs with guanine., Int. J. Mol. Sci., 21, 7645, 20201015
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  8. Contiguous 2,2,4-triamino-5(2H)-oxazolone obstructs DNA synthesis by DNA polymerases alpha, beta, eta, iota, kappa, REV1 and Klenow Fragment exo-, but not by DNA polymerase zeta., JOURNAL OF BIOCHEMISTRY, 20151021
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  9. Analysis of Nucleotide Insertion Opposite 2,2,4-Triamino-5(2H)‑oxazolone by Eukaryotic B- and Y‑Family DNA Polymerases., CHEMICAL RESEARCH IN TOXICOLOGY, 28(6), 1307-1316, 20150615
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