{"id":61,"date":"2025-03-26T13:21:52","date_gmt":"2025-03-26T04:21:52","guid":{"rendered":"https:\/\/dept.tus.ac.jp\/pcb-lab\/?page_id=61"},"modified":"2025-10-09T14:03:02","modified_gmt":"2025-10-09T05:03:02","slug":"publications","status":"publish","type":"page","link":"https:\/\/dept.tus.ac.jp\/pcb-lab\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"\n

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  1. Kawada, K., Takahashi, I., Takei, S., Nomura, A., Seto, Y., Fukui, K., and Asami, T. (2024) The Evaluation of Debranone Series Strigolactone Agonists for Germination Stimulants in Orobanche Species. J. Agric. Food Chem.<\/em> 72<\/strong>, 19517\u201319525<\/li>\n\n\n\n
  2. Okabe, S., Kitaoka, K., Suzuki, T., Kuruma, M., Hagihara, S., Yamaguchi, S., Fukui, K., and Seto, Y. (2023) Desmethyl type germinone, a specific agonist for the HTL\/KAI2 receptor, induces the Arabidopsis seed germination in a gibberellin-independent manner. Biochem Bioph Res Co<\/em>. 649<\/strong>, 110\u2013117<\/li>\n\n\n\n
  3. Fukui, K., Arai, K., Tanaka, Y., Aoi, Y., Kukshal, V., Jez, J. M., Kubes, M. F., Napier, R., Zhao, Y., Kasahara, H., and Hayashi, K. (2022) Chemical inhibition of the auxin inactivation pathway uncovers the roles of metabolic turnover in auxin homeostasis. Proc National Acad Sci<\/em>. 119<\/strong>, e2206869119<\/li>\n\n\n\n
  4. Takeuchi, J., Fukui, K., Seto, Y., Takaoka, Y., and Okamoto, M. (2021) Ligand\u2013receptor interactions in plant hormone signaling. Plant J<\/em>. 105<\/strong>, 290\u2013306<\/li>\n\n\n\n
  5. Hayashi, K., Arai, K., Aoi, Y., Tanaka, Y., Hira, H., Guo, R., Hu, Y., Ge, C., Zhao, Y., Kasahara, H., and Fukui, K. (2021) The main oxidative inactivation pathway of the plant hormone auxin. Nat Commun<\/em>. 12<\/strong>, 6752<\/li>\n\n\n\n
  6. Takahashi, I., Fukui, K., and Asami, T. (2020) On improving strigolactone mimics for induction of suicidal germination of the root parasitic plant Striga hermonthica. Abiotech<\/em>. 10.1007\/s42994-020-00031-0<\/li>\n\n\n\n
  7. Ohtaka, K., Yoshida, A., Kakei, Y., Fukui, K., Kojima, M., Takebayashi, Y., Yano, K., Imanishi, S., and Sakakibara, H. (2020) Difference Between Day and Night Temperatures Affects Stem Elongation in Tomato (Solanum lycopersicum) Seedlings via Regulation of Gibberellin and Auxin Synthesis. Front Plant Sci<\/em>. 11<\/strong>, 577235<\/li>\n\n\n\n
  8. Yesbolatova, A., Saito, Y., Kitamoto, N., Makino-Itou, H., Ajima, R., Nakano, R., Nakaoka, H., Fukui, K., Gamo, K., Tominari, Y., Takeuchi, H., Saga, Y., Hayashi, K., and Kanemaki, M. T. (2020) The auxin-inducible degron 2 technology provides sharp degradation control in yeast, mammalian cells, and mice. Nat Commun<\/em>. 11<\/strong>, 5701<\/li>\n\n\n\n
  9. Takubo, E., Kobayashi, M., Hirai, S., Aoi, Y., Ge, C., Dai, X., Fukui, K., Hayashi, K., Zhao, Y., and Kasahara, H. (2020) Role of Arabidopsis INDOLE-3-ACETIC ACID CARBOXYL METHYLTRANSFERASE 1 in auxin metabolism. Biochem. Biophys. Res. Commun.<\/em> 527<\/strong>, 1033\u20131038<\/li>\n\n\n\n
  10. Aoi, Y., Hira, H., Hayakawa, Y., Liu, H., Fukui, K., Dai, X., Tanaka, K., Hayashi, K., Zhao, Y., and Kasahara, H. (2020) UDP-glucosyltransferase UGT84B1 regulates the levels of indole-3-acetic acid and phenylacetic acid in Arabidopsis. Biochem. Biophys. Res. Commun.<\/em> 532<\/strong>, 244\u2013250<\/li>\n\n\n\n
  11. Oochi, A., Hajny, J., Fukui, K., Nakao, Y., Gallei, M., Quareshy, M., Takahashi, K., Kinoshita, T., Harborough, S. R., Kepinski, S., Kasahara, H., Napier, R. M., Friml, J., and Hayashi, K.-I. I. (2019) Pinstatic acid promotes auxin transport by inhibiting PIN internalization. Plant physiology<\/em>. 10.1104\/pp.19.00201<\/li>\n\n\n\n
  12. Fukui, K., Arai, K., Kasahara, H., Asami, T., and Hayashi, K. (2019) Synthetic agonist of HTL\/KAI2 shows potent stimulating activity for Arabidopsis seed germination. Bioorg Med Chem Lett<\/em>. 29<\/strong>, 2487\u20132492<\/li>\n\n\n\n
  13. Fukui, K., and Hayashi, K.-I. (2018) Manipulation and Sensing of Auxin Metabolism, Transport and Signaling. Plant cell Physiol.<\/em> 59<\/strong>, 1500\u20131510<\/li>\n\n\n\n
  14. Tsugafune, S., Mashiguchi, K., Fukui, K., Takebayashi, Y., Nishimura, T., Sakai, T., Shimada, Y., Kasahara, H., Koshiba, T., and Hayashi, K.-I. I. (2017) Yucasin DF, a potent and persistent inhibitor of auxin biosynthesis in plants. Scientific reports<\/em>. 7<\/strong>, 13992<\/li>\n\n\n\n
  15. Fukui, K., Yamagami, D., Ito, S., and Asami, T. (2017) A Taylor-Made Design of Phenoxyfuranone-Type Strigolactone Mimic. Frontiers in Plant Science<\/em>. 08<\/strong>, 936<\/li>\n\n\n\n
  16. Mashita, O., Koishihara, H., Fukui, K., Nakamura, H., and Asami, T. (2016) Discovery and identification of 2-methoxy-1-naphthaldehyde as a novel strigolactone-signaling inhibitor. J Pestic Sci<\/em>. 41<\/strong>, 71\u201378<\/li>\n\n\n\n
  17. Takahashi, I., Fukui, K., and Asami, T. (2016) Chemical modification of a phenoxyfuranone-type strigolactone mimic for selective effects on rice tillering or Striga hermonthica seed germination. Pest Manag Sci<\/em>. 72<\/strong>, 2048\u20132053<\/li>\n\n\n\n
  18. Ito, S., Nozoye, T., Sasaki, E., Imai, M., Shiwa, Y., Shibata-Hatta, M., Ishige, T., Fukui, K., Ito, K., Nakanishi, H., Nishizawa, N. K., Yajima, S., and Asami, T. (2015) Strigolactone regulates anthocyanin accumulation, acid phosphatases production and plant growth under low phosphate condition in Arabidopsis. PloS one<\/em>. 10<\/strong>, e0119724<\/li>\n\n\n\n
  19. Fukui, K., Ito, S., and Asami, T. (2013) Selective mimics of strigolactone actions and their potential use for controlling damage caused by root parasitic weeds. Molecular plant<\/em>. 6<\/strong>, 88\u201399<\/li>\n\n\n\n
  20. Nakamura, H., Xue, Y.-L. L., Miyakawa, T., Hou, F., Qin, H.-M. M., Fukui, K., Shi, X., Ito, E., Ito, S., Park, S.-H. H., Miyauchi, Y., Asano, A., Totsuka, N., Ueda, T., Tanokura, M., and Asami, T. (2013) Molecular mechanism of strigolactone perception by DWARF14. Nature communications<\/em>. 4<\/strong>, 2613<\/li>\n\n\n\n
  21. Tsubo, T., Chen, H.-H., Yokomori, M., Fukui, K., Kikuchi, S., and Yamada, T. (2012) Enantioselective Borohydride Reduction of Aliphatic Ketones Catalyzed by Ketoiminatocobalt(III) Complex with 1-Chlorovinyl Axial Ligand. Chemistry Letters<\/em>. 41<\/strong>, 780782<\/li>\n\n\n\n
  22. Fukui, K., Ito, S., Ueno, K., Yamaguchi, S., Kyozuka, J., and Asami, T. (2011) New branching inhibitors and their potential as strigolactone mimics in rice. Bioorganic & medicinal chemistry letters<\/em>. 21<\/strong>, 4905\u20138<\/li>\n\n\n\n
  23. Yoshida, S., Fukui, K., Kikuchi, S., and Yamada, T. (2010) Silver-Catalyzed Enantioselective Carbon Dioxide Incorporation into Bispropargylic Alcohols. J Am Chem Soc<\/em>. 132<\/strong>, 4072\u20134073<\/li>\n\n\n\n
  24. Yoshida, S., Fukui, K., Kikuchi, S., and Yamada, T. (2009) Silver-catalyzed Preparation of Oxazolidinones from Carbon Dioxide and Propargylic Amines. Chem Lett<\/em>. 38<\/strong>, 786\u2013787<\/li>\n<\/ol>\n\n\n\n

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