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European Journal of Medicinal Chemistry|November 17, 2018
Discovery, synthesis of novel fusidic acid derivatives possessed amino-terminal groups at the 3-hydroxyl position with anticancer activityJingxuan Ni, Mengqi Guo, Yucheng Cao, et al.
Toxicology and Applied Pharmacology|February 7, 2018
H6, a novel hederagenin derivative, reverses multidrug resistance in vitro and in vivoYanting Yang, Daokun Guan, Lei Lei, et al.
Oncotarget|May 12, 2016
Targeting radioresistant breast cancer cells by single agent CHK1 inhibitor via enhancing replication stressYao Zhang, Jinzhi Lai, Zhanwen Du, et al.
Journal of Ophthalmology|August 25, 2020
Portable Handheld Slit-Lamp Based on a Smartphone Camera for Cataract ScreeningShenming Hu, Hong Wu, Xinze Luan, et al.
Theranostics|December 11, 2024
Low PPP2R2A expression promotes sensitivity to CHK1 inhibition in high-grade serous ovarian cancerZhaojun Qiu, Deepika Sigh, Yujie Liu, et al.
The Journal of Clinical Investigation|December 18, 2025
PPP2R2A insufficiency enhances PD-L1 immune checkpoint blockade efficacy in lung cancer through cGAS-STING activationZhaojun Qiu, No-Joon Song, Anqi Li, et al.
Cell Death & Disease|July 8, 2026
L-2-Hydroxyglutarate sensitizes ferroptosis through ATF3/CHAC1-mediated glutathione degradation in hepatocellular carcinomaCaixia Xi, Junfeng Pang, Mohammad Oliaeimotlagh, et al.
Analytical Biochemistry|January 9, 2016
Building homogeneous time-resolved fluorescence resonance energy transfer assays for characterization of bivalent inhibitors of an inhibitor of apoptosis protein targetCharu Chaudhry, Jonathan Davis, Yong Zhang, et al.
Acta Crystallographica. Section D, Structural Biology|May 4, 2016
Crystal structures of apo and inhibitor-bound TGFβR2 kinase domain: insights into TGFβR isoform selectivityAndrew J Tebben, Maxim Ruzanov, Mian Gao, et al.
Scientific Reports|July 8, 2024
Agreement and repeatability of scotopic pupil size measurement with the 2WIN-S portable refractor in Chinese adultsYibing Zhou, Xingru He, Ziming Liu, et al.
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