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Seong Who Kim

Researcher at University of Ulsan

Publications -  93
Citations -  12875

Seong Who Kim is an academic researcher from University of Ulsan. The author has contributed to research in topics: Mesenchymal stem cell & Autophagy. The author has an hindex of 30, co-authored 91 publications receiving 10960 citations. Previous affiliations of Seong Who Kim include Asan Medical Center.

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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

Daniel J. Klionsky, +2522 more
- 21 Jan 2016 - 
TL;DR: In this paper, the authors present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macro-autophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
Journal ArticleDOI

Guidelines for the use and interpretation of assays for monitoring autophagy

Daniel J. Klionsky, +1287 more
- 01 Apr 2012 - 
TL;DR: These guidelines are presented for the selection and interpretation of methods for use by investigators who aim to examine macroautophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
Journal ArticleDOI

Comparative Analysis of Human Mesenchymal Stem Cells from Bone Marrow, Adipose Tissue, and Umbilical Cord Blood as Sources of Cell Therapy

TL;DR: It is found that recombinant Ang-1 as potential soluble paracrine factor or its small interference RNA (siRNA) was responsible for this beneficial effect in part by preventing inflammation.
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Bromocriptine activates NQO1 via Nrf2-PI3K/Akt signaling: novel cytoprotective mechanism against oxidative damage.

TL;DR: It is shown that bromocriptine upregulates the expression and activity of NQO1, attenuates the increase in the protein-bound quinone in H(2)O(2)-treated PC 12 cells, and protects PC12 cells against oxidative damage.
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miR-140-5p suppresses BMP2-mediated osteogenesis in undifferentiated human mesenchymal stem cells

TL;DR: It is proposed that miR‐140‐5p functionally inhibits osteogenic lineage commitment in undifferentiated hMSCs and increases the expression of BMP signaling components and critical regulators of osteogenic differentiation.