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Da Hye Lee

Researcher at Chungnam National University

Publications -  10
Citations -  604

Da Hye Lee is an academic researcher from Chungnam National University. The author has contributed to research in topics: Hippo signaling pathway & Lung cancer. The author has an hindex of 5, co-authored 9 publications receiving 435 citations. Previous affiliations of Da Hye Lee include KAIST.

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YAP/TAZ regulates sprouting angiogenesis and vascular barrier maturation

TL;DR: Results show that YAP/TAZ plays multifaceted roles for EC behaviors, proliferation, junction assembly, and metabolism in sprouting angiogenesis and barrier formation and maturation and could be a potential therapeutic target for treating neovascular diseases.
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LATS-YAP/TAZ controls lineage specification by regulating TGFβ signaling and Hnf4α expression during liver development

TL;DR: It is reported that the Hippo pathway controls liver cell lineage specification and proliferation separately from Notch signalling, using mice and primary hepatoblasts with liver-specific knockout of Lats1 and Lats2 kinase, the direct upstream regulators of YAP and TAZ.
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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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Ablation of Rassf2 induces bone defects and subsequent haematopoietic anomalies in mice

TL;DR: It is shown that Rassf2 knockout mice manifest a multisystemic phenotype including haematopoietic anomalies and defects in bone remodelling and that RASSF2 regulates osteoblast and osteoclast differentiation by inhibiting NF‐κB signalling.
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Circulating regulatory T cells predict efficacy and atypical responses in lung cancer patients treated with PD-1/PD-L1 inhibitors

TL;DR: In this paper, the frequency of pseudoprogression and hyperprogression in lung cancer patients treated with ICIs in the real world and aimed to discover a novel candidate marker to distinguish pseudOProgression from hyper-progression soon after ICI treatment.