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Wen-Hsiung Chan

Researcher at Chung Yuan Christian University

Publications -  51
Citations -  1895

Wen-Hsiung Chan is an academic researcher from Chung Yuan Christian University. The author has contributed to research in topics: Apoptosis & Reactive oxygen species. The author has an hindex of 21, co-authored 48 publications receiving 1712 citations. Previous affiliations of Wen-Hsiung Chan include Chang Gung University.

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Fluorescent gold nanoclusters as a biocompatible marker for in vitro and in vivo tracking of endothelial cells.

TL;DR: In vivo study using hindlimb ischemic mice with an intramuscular injection of FANC-labeled human EPC showed that the cells preserved an angiogenic potential and exhibited traceable signals after 21 days, demonstrating that FANC is a promising biocompatible fluorescent probe.
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Curcumin inhibits UV irradiation‐induced oxidative stress and apoptotic biochemical changes in human epidermoid carcinoma A431 cells

TL;DR: It is demonstrated that curcumin (Cur), the yellow pigment of Curcuma longa with known anti‐oxidant and anti‐inflammatory properties, can prevent UV irradiation‐induced apoptotic changes, including c‐Jun N‐terminal kinase (JNK) activation, loss of mitochondrial membrane potential (MMP), mitochondrial release of cytochrome C, caspase‐3 activation, and cleavage/activation of PAK2 in A431 cells.
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Curcumin prevents methylglyoxal-induced oxidative stress and apoptosis in mouse embryonic stem cells and blastocysts.

TL;DR: The hypothesis that curcumin inhibits MG‐induced apoptosis in mouse ESC‐B5 cells and blastocysts by blocking ROS formation and subsequent apoptotic biochemical events is supported.

Synthesis of Fluorescent Metallic Nanoclusters toward Biomedical Application: Recent Progress and Present Challenges

TL;DR: In this review, a new class of fluorescent labels by biocognition molecules to fluorescent noble-metal nanoclusters such as Au and Ag are produced, which are more biocompatible and stable against photobleaching compared with organic dyes and are ideal fluorophores for multicolor and multiplexing applications in biomedical engineering and molecular biotechnology.
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Apoptotic signaling in methylglyoxal-treated human osteoblasts involves oxidative stress, c-Jun N-terminal kinase, caspase-3, and p21-activated kinase 2.

TL;DR: It is shown for the first time that MG treatment triggers apoptosis in osteoblasts via specific apoptotic signaling, and causes BMD loss in vivo.