K
Kiyonori Takegoshi
Researcher at Kyoto University
Publications - 186
Citations - 5083
Kiyonori Takegoshi is an academic researcher from Kyoto University. The author has contributed to research in topics: Solid-state nuclear magnetic resonance & Nuclear magnetic resonance spectroscopy. The author has an hindex of 30, co-authored 186 publications receiving 4666 citations. Previous affiliations of Kiyonori Takegoshi include Mie University & Tokyo Metropolitan University.
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dipolar-assisted rotational resonance in magic-angle spinning NMR
TL;DR: In this article, a new 13 C -13 C recoupling mechanism was proposed for band-selective recouplings between carbonyl/aromatic carbons and aliphatic carbons under magic-angle spinning.
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13C–1H dipolar-driven 13C–13C recoupling without 13C rf irradiation in nuclear magnetic resonance of rotating solids
TL;DR: In this article, the average Hamiltonian theory has been used for 13C-1H dipolar-assisted rotational resonance (DARR) and 13C−1H line broadening.
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An oxyhydride of BaTiO3 exhibiting hydride exchange and electronic conductivity
Yoji Kobayashi,Olivier Hernandez,Tatsunori Sakaguchi,Takeshi Yajima,Thierry Roisnel,Yoshihiro Tsujimoto,Masaki Morita,Yasuto Noda,Yuuki Mogami,Atsushi Kitada,Masatoshi Ohkura,Saburo Hosokawa,Zhaofei Li,Katsuro Hayashi,Yoshihiro Kusano,Jungeun Kim,Naruki Tsuji,Akihiko Fujiwara,Yoshitaka Matsushita,Kazuyoshi Yoshimura,Kiyonori Takegoshi,Masashi Inoue,Mikio Takano,Hiroshi Kageyama +23 more
TL;DR: This work presents an oxyhydride of the perhaps most well-known perovskite, BaTiO(3), as an O(2-)/H(-) solid solution with hydride concentrations up to 20% of the anion sites, which is electronically conducting, and stable in air and water at ambient conditions.
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Site-Specific Inhibitory Mechanism for Amyloid-β42 Aggregation by Catechol-Type Flavonoids Targeting the Lys Residues
Mizuho Sato,Kazuma Murakami,Mayumi Uno,Yu Nakagawa,Sumie Katayama,Ken Ichi Akagi,Yuichi Masuda,Yuichi Masuda,Kiyonori Takegoshi,Kazuhiro Irie +9 more
TL;DR: It is demonstrated that catechol-type flavonoids could specifically suppress Aβ42 aggregation by targeting Lys residues, and the mechanism that the o-quinone reacts with Lys residues of A β42 might be more intrinsic.
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Structure of β-amyloid fibrils and its relevance to their neurotoxicity: Implications for the pathogenesis of Alzheimer’s disease
Kazuhiro Irie,Kazuma Murakami,Yuichi Masuda,Akira Morimoto,Hajime Ohigashi,Ryutaro Ohashi,Kiyonori Takegoshi,Masaya Nagao,Takahiko Shimizu,Takuji Shirasawa +9 more
TL;DR: A review summarizes mainly the own recent findings from the structural analysis of Aβ42 fibrils and discusses its relevance to their neurotoxicity in vitro.