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Journal of Medicinal Chemistry|November 21, 2019
Structure-Based Discovery of SD-36 as a Potent, Selective, and Efficacious PROTAC Degrader of STAT3 ProteinHaibin Zhou, Longchuan Bai, Renqi Xu, et al.
Plant Biotechnology Journal|March 25, 2026
CitPH4 Confers Resistance to Citrus Canker by Activating Papain-Like Cysteine ProteaseTao Yuan, Rongyan Huang, Zhihao Lu, et al.
Journal of Medicinal Chemistry|July 18, 2018
Structure-Based Discovery of CF53 as a Potent and Orally Bioavailable Bromodomain and Extra-Terminal (BET) Bromodomain InhibitorYujun Zhao, Bing Zhou, Longchuan Bai, et al.
Cancer Research|February 18, 2017
Targeted Degradation of BET Proteins in Triple-Negative Breast CancerLongchuan Bai, Bing Zhou, Chao-Yie Yang, et al.
Cancer Research|August 23, 2014
SAR405838: an optimized inhibitor of MDM2-p53 interaction that induces complete and durable tumor regressionShaomeng Wang, Wei Sun, Yujun Zhao, et al.
Acta Pharmaceutica Sinica. B|February 23, 2023
PRMT6 promotes tumorigenicity and cisplatin response of lung cancer through triggering 6PGD/ENO1 mediated cell metabolismMingming Sun, Leilei Li, Yujia Niu, et al.
Microscopy and Microanalysis : the Official Journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada|September 3, 2024
Towards Establishing Best Practice in the Analysis of Hydrogen and Deuterium by Atom Probe TomographyBaptiste Gault, Aparna Saksena, Xavier Sauvage, et al.
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