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Tomomi Ide

Researcher at Kyushu University

Publications -  205
Citations -  8824

Tomomi Ide is an academic researcher from Kyushu University. The author has contributed to research in topics: Heart failure & Medicine. The author has an hindex of 44, co-authored 171 publications receiving 7318 citations. Previous affiliations of Tomomi Ide include Kumamoto University & University of Pennsylvania.

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Mitochondrial Electron Transport Complex I Is a Potential Source of Oxygen Free Radicals in the Failing Myocardium

TL;DR: Direct evidence is provided for the involvement of ROS in the mitochondrial origin of HF myocytes, which might be responsible for both contractile dysfunction and structural damage to the myocardium.
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Mitochondrial DNA damage and dysfunction associated with oxidative stress in failing hearts after myocardial infarction.

TL;DR: It is hypothesized that ROS may induce mitochondrial DNA (mtDNA) damage, which leads to defects of mtDNA-encoded gene expression and respiratory chain complex enzymes and thus may contribute to the progression of left ventricular remodeling and failure after myocardial infarction.
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Direct Evidence for Increased Hydroxyl Radicals Originating From Superoxide in the Failing Myocardium

TL;DR: There was a significant positive relation between myocardial ROS level and left ventricular contractile dysfunction and, in the failing myocardium, *OH was produced as a reactive product of *O(2)(-) and H(2)O( 2), which might play an important role inleft ventricular failure.
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Treatment With Dimethylthiourea Prevents Left Ventricular Remodeling and Failure After Experimental Myocardial Infarction in Mice Role of Oxidative Stress

TL;DR: The attenuation of increased myocardial ROS and metalloproteinase activity with DMTU may contribute, at least in part, to its beneficial effects on LV remodeling and failure.
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Biosynthesis of 15-deoxy-Δ12,14-PGJ2 and the ligation of PPARγ

TL;DR: In this paper, the 15-deoxy-Delta12,14-PGJ2 (15d)-Ligand was identified as an endogenous ligand for PPARgamma, inducing adipogenesis in vitro.