Hideo Kimura focuses on Biochemistry, Cystathionine beta synthase, Cysteine, Hydrogen sulfide and Cell biology. Sulfurtransferase, Oxidative stress, Long-term potentiation, Intracellular and Glutathione are the core of his Biochemistry study. His work carried out in the field of Cystathionine beta synthase brings together such families of science as NMDA receptor, Internal medicine, Endocrinology and Genomic library.
Hideo Kimura studied Cysteine and Cytoplasm that intersect with Peroxisome and Kidney metabolism. The concepts of his Hydrogen sulfide study are interwoven with issues in Thioredoxin, Thoracic aorta and Photochemistry. His studies in Cell biology integrate themes in fields like Cell culture and Endogeny.
His primary scientific interests are in Biochemistry, Internal medicine, Hydrogen sulfide, Cell biology and Cystathionine beta synthase. His Biochemistry study typically links adjacent topics like Biophysics. The study incorporates disciplines such as Gastroenterology, Endocrinology and Cardiology in addition to Internal medicine.
His research integrates issues of Cytoprotection, Photochemistry, Signal transduction and Nitric oxide in his study of Hydrogen sulfide. His biological study spans a wide range of topics, including Cell culture and Endogeny. His Cystathionine beta synthase research is multidisciplinary, incorporating perspectives in NMDA receptor, Long-term potentiation and Hippocampal formation.
His main research concerns Biochemistry, Hydrogen sulfide, Cysteine, Sulfurtransferase and Cystathionine beta synthase. Biochemistry is closely attributed to Cell biology in his study. His Hydrogen sulfide study integrates concerns from other disciplines, such as Cytoprotection, Biophysics, Photochemistry, Molecule and Nitric oxide.
His Cysteine research incorporates elements of Thiosulfate, Receptor, Transient receptor potential channel, Stereochemistry and Redox. His research in Sulfurtransferase intersects with topics in Recombinant DNA, Substrate, Rhodanese and Active site. Hideo Kimura has researched Cystathionine beta synthase in several fields, including Oxidase test and Oxidative phosphorylation.
Hideo Kimura mainly investigates Biochemistry, Sulfurtransferase, Cysteine, Cystathionine beta synthase and Hydrogen sulfide. In his study, HEK 293 cells is strongly linked to Cell biology, which falls under the umbrella field of Biochemistry. His work deals with themes such as Cysteine metabolism, Cell signaling, COS cells and Recombinant DNA, which intersect with Sulfurtransferase.
The various areas that Hideo Kimura examines in his Cysteine study include Rhodanese, Biophysics, Active site, Receptor and Nitric oxide. Hideo Kimura usually deals with Cystathionine beta synthase and limits it to topics linked to Oxidase test and Kidney and Hydrogen peroxide. His Hydrogen sulfide study incorporates themes from Cytoprotection, Thioredoxin, Mediator and Cystathionine gamma-lyase.
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The possible role of hydrogen sulfide as an endogenous neuromodulator
Kazuho Abe;Hideo Kimura.
The Journal of Neuroscience (1996)
The Possible Role of Hydrogen Sulfide as an Endogenous Smooth Muscle Relaxant in Synergy with Nitric Oxide
Rumiko Hosoki;Norio Matsuki;Hideo Kimura.
Biochemical and Biophysical Research Communications (1997)
Hydrogen sulfide attenuates myocardial ischemia-reperfusion injury by preservation of mitochondrial function
John W. Elrod;John W. Calvert;Joanna Morrison;Jeannette E. Doeller.
Proceedings of the National Academy of Sciences of the United States of America (2007)
3-Mercaptopyruvate sulfurtransferase produces hydrogen sulfide and bound sulfane sulfur in the brain.
Norihiro Shibuya;Makiko Tanaka;Mikiharu Yoshida;Yuki Ogasawara.
Antioxidants & Redox Signaling (2009)
Mechanism of Cellular 3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide (MTT) Reduction
Yuanbin Liu;Daniel A. Peterson;Hideo Kimura;David Schubert.
Journal of Neurochemistry (2002)
Hydrogen sulfide protects neurons from oxidative stress.
Yuka Kimura;Hideo Kimura.
The FASEB Journal (2004)
Brain hydrogen sulfide is severely decreased in Alzheimer's disease.
Ko Eto;Takashi Asada;Kunimasa Arima;Takao Makifuchi.
Biochemical and Biophysical Research Communications (2002)
Hydrogen sulfide: its production, release and functions
Amino Acids (2011)
Hydrogen sulfide increases glutathione production and suppresses oxidative stress in mitochondria.
Yuka Kimura;Yu-Ichi Goto;Hideo Kimura.
Antioxidants & Redox Signaling (2010)
Hypoxia response element of the human vascular endothelial growth factor gene mediates transcriptional regulation by nitric oxide: control of hypoxia-inducible factor-1 activity by nitric oxide
Hideo Kimura;Alessandro Weisz;Yukiko Kurashima;Kouichi Hashimoto.
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