H
Hiroshi Maeda
Researcher at Kumamoto University
Publications - 915
Citations - 67944
Hiroshi Maeda is an academic researcher from Kumamoto University. The author has contributed to research in topics: Neocarzinostatin & Nitric oxide. The author has an hindex of 103, co-authored 893 publications receiving 63370 citations. Previous affiliations of Hiroshi Maeda include Osaka University & Okayama University.
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Kinetics of binding of oligosaccharides to a homogeneous pneumococcal antibody: dependence on antigen chain length suggests a labile intermediate complex.
TL;DR: Temperature-jump experiments were performed with di, tetra-, and hexasaccharides derived from type III pneumococcal polysaccharide using a homogeneous corresponding antibody IgG 45-394 and a mechanism is proposed which consists of a fast formation of a labile oligosaccharide-antibody precomplex followed by a slow isomerization step which is induced by the oligosACcharide ligands but which is chain-length independent.
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Vasodilator effect of carboxy-2-phenyl-4,4,5,5-tetramethylimidazoline-1-oxyl in the coronary circulation: in vivo and in vitro studies
Ryusuke Tsunoda,Ken Okumura,Hiroshi Ishizaka,Toshiro Matsunaga,Toshifumi Tabuchi,Hirofumi Yasue,Takaaki Akaike,Keizo Sato,Hiroshi Maeda +8 more
TL;DR: The results of the in vitro experiment suggested that the activation of soluble guanylate cyclase of the vascular smooth muscle cell may be involved, at least in part, in the vasodilator mechanism of carboxy-PTI in large conduit arteries.
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Cu-Ag wire pulsed magnets with and without internal reinforcements
Toshihisa Asano,Y. Sakai,Mitsutake Oshikiri,Kiyoshi Inoue,Hiroshi Maeda,G. Heremans,L. Van Bockstal,L. Li,Fritz Herlach +8 more
TL;DR: In this article, a newly developed Cu-Ag microcomposite wire which has excellent properties of high conductivity, high mechanical strength and high homogeneity along the wire was used to construct magnet coils for pulsed magnets with long pulse duration.
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Degradation pathway of kinins in tumor ascites and inhibition by kininase inhibitors: analysis by HPLC.
TL;DR: The results indicate the presence of other metalloprotease(s) which cleaves kinins in the ascitic fluid, in addition to kininase I and Kininase II.
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Targeting of heat-shock protein 32/heme oxygenase-1 in canine mastocytoma cells is associated with reduced growth and induction of apoptosis
Emir Hadzijusufovic,Laura Rebuzzi,Karoline V. Gleixner,Veronika Ferenc,Barbara Peter,Rudin Kondo,Alexander Gruze,Michael Kneidinger,Maria Theresa Krauth,Matthias Mayerhofer,Puchit Samorapoompichit,Khaled Greish,Arun K. Iyer,Winfried F. Pickl,Hiroshi Maeda,Michael Willmann,Peter Valent +16 more
TL;DR: It is reported that heat-shock protein 32 (Hsp32), also known as heme oxygenase-1, is a survival-enhancing molecule and new target in canine mastocytoma cells.