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Chulhee Choi

Researcher at KAIST

Publications -  200
Citations -  7862

Chulhee Choi is an academic researcher from KAIST. The author has contributed to research in topics: Apoptosis & Tumor necrosis factor alpha. The author has an hindex of 47, co-authored 189 publications receiving 6740 citations. Previous affiliations of Chulhee Choi include Yonsei University & University of Alabama at Birmingham.

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Regulation of PDGF signalling and vascular remodelling by peroxiredoxin II

TL;DR: Prx II deficiency results in increased production of H2O2, enhanced activation of PDGF receptor (PDGFR) and phospholipase Cγ1, and subsequently increased cell proliferation and migration in response to PDGF, demonstrating a localized role for endogenous H2 O2 in PDGF signalling, and indicating a biological function of Prx II in cardiovascular disease.
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Exosome engineering for efficient intracellular delivery of soluble proteins using optically reversible protein–protein interaction module

TL;DR: A new tool for intracellular delivery of target proteins, named ‘exosomes for protein loading via optically reversible protein–protein interactions’ (EXPLORs), which is able to successfully load cargo proteins into newly generated exosomes using optogenetic control of protein-protein interactions between the cargo and an exosome-localized partner.
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Fas ligand/Fas system in the brain: regulator of immune and apoptotic responses

TL;DR: The FasL-Fas system should be considered as a double-edged sword in the CNS: maintaining the immune suppressed status in normal brain and inducing neuronal cell death and inflammation in a variety of neurologic disorders.
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Continuous blood cell separation by hydrophoretic filtration

TL;DR: The device can be useful for the binary separation of a wide range of biological particles by size and offers potential for a power-free cell sorter to be integrated into disposable lab-on-a-chip devices.
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Role of NADPH oxidase 4 in lipopolysaccharide-induced proinflammatory responses by human aortic endothelial cells

TL;DR: Nox4 plays a central role in LPS-induced proinflammatory responses by endothelial cells in an ROS-dependent manner.