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Tae Woong Kim

Researcher at Kangwon National University

Publications -  51
Citations -  1956

Tae Woong Kim is an academic researcher from Kangwon National University. The author has contributed to research in topics: Syk & Proto-oncogene tyrosine-protein kinase Src. The author has an hindex of 25, co-authored 51 publications receiving 1779 citations. Previous affiliations of Tae Woong Kim include UPRRP College of Natural Sciences.

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Cordycepin inhibits lipopolysaccharide-induced inflammation by the suppression of NF-κB through Akt and p38 inhibition in RAW 264.7 macrophage cells

TL;DR: Results suggest that cordycepin inhibits the production of NO production by down-regulation of iNOS and COX-2 gene expression via the suppression of NF-kappaB activation, Akt and p38 phosphorylation, and may provide a potential therapeutic approach for inflammation-associated disorders.
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Differential regulation of NO availability from macrophages and endothelial cells by the garlic component S-allyl cysteine.

TL;DR: It is demonstrated that garlic extract and SAC, due to their antioxidant activity, differentially regulate NO production by inhibiting iNOS expression in macrophages while increasing NO in endothelial cells, which may contribute to the anti-inflammatory effect and prevention of atherosclerosis by these reagents.
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Phellinus linteus inhibits inflammatory mediators by suppressing redox-based NF-κB and MAPKs activation in lipopolysaccharide-induced RAW 264.7 macrophage

TL;DR: It is suggested that PLBF inhibits the production of NO and PGE2 through the down-regulation of iNOS and COX-2 gene expression via ROS-based NF-kappaB and MAPKs activation, and may provide a potential therapeutic approach for inflammation-associated disorders.
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Cordycepin-induced apoptosis and autophagy in breast cancer cells are independent of the estrogen receptor

TL;DR: It is demonstrated that cordycepin effectively kills MDA-MB-231 and MCF-7 human breast cancer cell lines in culture and should be considered a clinically useful, ER-independent, chemotherapeutic agent for human Breast cancer.
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In vitro and in vivo anti-inflammatory activities of Polygonum hydropiper methanol extract.

TL;DR: Ph-ME exerts strong anti-inflammatory activity by suppressing Src/Syk/NF-κB and IRAK/AP-1/CREB pathways, which contribute to its major ethno-pharmacological role as an anti-gastritis remedy.