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Jong Woo Kim

Researcher at Electronics and Telecommunications Research Institute

Publications -  24
Citations -  377

Jong Woo Kim is an academic researcher from Electronics and Telecommunications Research Institute. The author has contributed to research in topics: Thin-film transistor & Oxide thin-film transistor. The author has an hindex of 10, co-authored 24 publications receiving 311 citations. Previous affiliations of Jong Woo Kim include Myongji University.

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The Cyclic Peptide Ecumicin Targeting ClpC1 Is Active against Mycobacterium tuberculosis In Vivo

TL;DR: Genome mining of lab-generated, spontaneous ecumicin-resistant M. tuberculosis strains identified the ClpC1 ATPase complex as the putative target, and this was confirmed by a drug affinity response test, and ecumICin may serve as a lead compound for anti-TB drug development.
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Platycodin D, a triterpenoid sapoinin from Platycodon grandiflorum, ameliorates cisplatin-induced nephrotoxicity in mice.

TL;DR: In histopathological examination, pretreatment with PD showed ameliorated renal injury such as intraluminal cast formation and epithelial desquamation and over-expression of nuclear factor-kappa B p65 and apoptotic cells were suppressed by PD pretreatment.
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Triterpenoid Saponins Isolated from Platycodon grandiflorum Inhibit Hepatitis C Virus Replication.

TL;DR: It is demonstrated that combinatorial treatment of PGSM and IFN-α efficiently suppressed colony formation with significant reduction in drug resistant variant of HCV, suggesting that triterpenoid saponin may represent a novel anti-HCV therapeutic agent.
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An efficient approach for cloning the dNDP‐glucose synthase gene from actinomycetes and its application in Streptomyces spectabilis, a spectinomycin producer

TL;DR: By DNA sequence analysis, seven amplified fragments showed high homology with dTDP-glucose synthase genes that participate in the biosynthesis of secondary metabolites or in deoxy-sugar moieties in lipopolysaccharides.
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Talosins A and B: new isoflavonol glycosides with potent antifungal activity from Kitasatospora kifunensis MJM341. I. Taxonomy, fermentation, isolation, and biological activities.

TL;DR: These talosins are the first isoflavonol glycosides with a 6-deoxy-talose sugar component and they may be useful as antifungal agents with low toxicity because of no visible cytotoxicity against the human hepatic HepG2 cell.