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Quan Chen

Researcher at Nankai University

Publications -  244
Citations -  20608

Quan Chen is an academic researcher from Nankai University. The author has contributed to research in topics: Medicine & Mitochondrion. The author has an hindex of 52, co-authored 154 publications receiving 16697 citations. Previous affiliations of Quan Chen include Chinese Academy of Fishery Sciences & Chinese Academy of Sciences.

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High autophagic flux guards ESC identity through coordinating autophagy machinery gene program by FOXO1.

TL;DR: It is shown that mouse ESCs exhibit a high autophagic flux that is maintained by coordinating expression of autophagy core molecular machinery genes through FOXO1, a forkhead family transcription factor.
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Role of Ca2+ signaling in initiation of stretch-induced apoptosis in neonatal heart cells.

TL;DR: It is concluded that stretch-induced Ca( 2+) entry, via the Ca(2+)-induced Ca (2+) release mechanism, plays an important role in initiating apoptotic signaling during mechanical stress.
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G-protein β2 subunit interacts with mitofusin 1 to regulate mitochondrial fusion.

TL;DR: It is reported that guanine nucleotide binding protein-β subunit 2 (Gβ2), a WD40 repeats protein and a member of the β-subunits of the heterotrimeric G proteins, has a crucial function in mitochondrial fusion.
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Cytotoxic Activities of New Jadomycin Derivatives

TL;DR: Structural-activity-relationship analyses clearly demonstrate that the side chains of the oxazolone ring derived from the incorporated amino acids make a significant impact on biological activity and jadomycin offers an ideal scaffold to manipulate structure and could be exploited to make many novel bioactive compounds with altered activities.
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Redox status of thioredoxin-1 (TRX1) determines the sensitivity of human liver carcinoma cells (HepG 2) to arsenic trioxide-induced cell death

TL;DR: TRX1 plays a central role in regulating apoptosis by blocking cyto c release, and inactivation of TRX1 by either mutation or oxidization of the active site cysteines may sensitize tumor cells to As2O3-induced apoptosis.