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Young Mi Kim

Researcher at Pusan National University

Publications -  146
Citations -  2262

Young Mi Kim is an academic researcher from Pusan National University. The author has contributed to research in topics: Prodrug & Aminosalicylic acid. The author has an hindex of 24, co-authored 136 publications receiving 2053 citations.

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Sphingosylphosphorylcholine induces differentiation of human mesenchymal stem cells into smooth-muscle-like cells through a TGF-β-dependent mechanism

TL;DR: SPC induces differentiation of human adipose-tissue-derived mesenchymal stem cells to smooth-muscle-like cell types through Gi/o-ERK-dependent autocrine secretion of TGF-β, which activates a Smad2-SRF/myocardin-dependent pathway.
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Cancer‐Derived Lysophosphatidic Acid Stimulates Differentiation of Human Mesenchymal Stem Cells to Myofibroblast‐Like Cells

TL;DR: It is suggested that cancer‐derived LPA stimulates differentiation of hADSCs to myofibroblast‐like cells and increases SDF‐1 expression through activating autocrine TGF‐β1‐Smad signaling pathway.
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Metabolic and Pharmacological Properties of Rutin, a Dietary Quercetin Glycoside, for Treatment of Inflammatory Bowel Disease

TL;DR: The data suggest that rutin acted as a quercetin deliverer to the large intestine and its anti-inflammatory action in TNBS-induced colitis rats may be through quercETin-mediated inhibition of TNF-α-induced NFκB activation.
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Angiotensin II-induced differentiation of adipose tissue-derived mesenchymal stem cells to smooth muscle-like cells

TL;DR: The results suggest that Ang II induces differentiation of human adipose tissue-derived mesenchymal stem cells to contractile smooth muscle-like cells through ERK-dependent activation of the autocrine TGF-beta1-Smad2 crosstalk pathway.
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A Rho Kinase/Myocardin-Related Transcription Factor-A–Dependent Mechanism Underlies the Sphingosylphosphorylcholine-Induced Differentiation of Mesenchymal Stem Cells Into Contractile Smooth Muscle Cells

TL;DR: The results suggest that SPC induced differentiation of hADSCs into contractile SMCs through a mechanism involving RhoA/Rho kinase–dependent nuclear translocation of MRTF-A, and pharmacological inhibition of Rho Kinase blocked this effect.