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Yuzuru Ishimura

Researcher at Keio University

Publications -  149
Citations -  6653

Yuzuru Ishimura is an academic researcher from Keio University. The author has contributed to research in topics: Cytochrome & Heme. The author has an hindex of 42, co-authored 149 publications receiving 6550 citations. Previous affiliations of Yuzuru Ishimura include University of Texas Health Science Center at San Antonio & Tribhuvan University.

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The low-spin heme of cytochrome c oxidase as the driving element of the proton-pumping process

TL;DR: It is reported that the Asp-51 → Asn mutation of the bovine enzyme abolishes its proton-pumping function without impairment of the dioxygen reduction activity.
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Induction of Heme Oxygenase-1 Suppresses Venular Leukocyte Adhesion Elicited by Oxidative Stress Role of Bilirubin Generated by the Enzyme

TL;DR: Results indicate that induction of the HO-1 activity serves as a potential stratagem to prevent oxidant-induced microvascular leukocyte adhesion through the action of bilirubin, a product of HO reaction.
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Uncoupling of the cytochrome P-450cam monooxygenase reaction by a single mutation, threonine-252 to alanine or valine: possible role of the hydroxy amino acid in oxygen activation.

TL;DR: Site-directed mutants of cytochrome P-450cam, in which threonine-252 had been changed to alanine, valine, or serine, were employed to study the role of the hydroxy amino acid in the monooxygenase reaction, exhibited optical absorption spectra almost indistinguishable from those of the wild-type enzyme in their ferric, ferrous, oxygenated, and carbon monoxide ferrous forms.
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Distribution of heme oxygenase isoforms in rat liver. Topographic basis for carbon monoxide-mediated microvascular relaxation.

TL;DR: It is suggested that CO evolved by HO-2 in the parenchymal cells, and, released to the extrasinusoidal space, served as the physiological relaxant for hepatic sinusoids.
Journal Article

Activation of a suicide process of thymocytes through DNA fragmentation by calcium ionophores and phorbol esters.

TL;DR: TPA switched a suicide process induced by A23187 to an opposite process: stimulation of DNA synthesis, suggesting that the signals by protein kinases and calcium ions may regulate both cell proliferation and death, independently, synergistically or antagonistically.