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Chaeuk Chung

Researcher at Chungnam National University

Publications -  83
Citations -  1739

Chaeuk Chung is an academic researcher from Chungnam National University. The author has contributed to research in topics: Medicine & Lung cancer. The author has an hindex of 17, co-authored 67 publications receiving 1143 citations. Previous affiliations of Chaeuk Chung include KAIST.

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Yap- and Cdc42-dependent nephrogenesis and morphogenesis during mouse kidney development

TL;DR: It is proposed that Yap responds to Cdc42-dependent signals in nephron progenitor cells to activate a genetic program required to shape the functioning nephrons, in a manner independent of regulation of cell proliferation and apoptosis.
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COVID-19 Patients Upregulate Toll-like Receptor 4-mediated Inflammatory Signaling That Mimics Bacterial Sepsis.

TL;DR: It is reported here that toll-like receptor (TLR) 4-mediated inflammatory signaling molecules are upregulated in peripheral blood mononuclear cells from COVID-19 patients, compared with healthy controls (HC).
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Hippo effector YAP directly regulates the expression of PD-L1 transcripts in EGFR-TKI-resistant lung adenocarcinoma.

TL;DR: Surprisingly, knockdown of PD-L1 was sufficient to decrease cell proliferation and wound healing in the EGFR-TKI-resistant PC9 cells, suggesting a PD1-independent oncogenic function of PD -L1.
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MIR144* inhibits antimicrobial responses against Mycobacterium tuberculosis in human monocytes and macrophages by targeting the autophagy protein DRAM2

TL;DR: This study shows that Mtb significantly induces the expression of MIR144*/hsa-miR-144-5p, which targets the 3′-untranslated region of DRAM2 (DNA damage regulated autophagy modulator 2) in human monocytes and macrophages, and reveals that DR AM2 is a key coordinator of autophagic activation that enhances antimicrobial activity against Mtb.
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Autophagy: A new strategy for host-directed therapy of tuberculosis

TL;DR: Understanding the mechanisms and key players involved in modulating antibacterial autophagy will provide innovative improvements in anti-TB therapy via an autophophagy-targeting approach.