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International Journal of Clinical and Experimental Pathology|January 15, 2020
A single nucleotide polymorphism CTSB rs12898 is associated with primary hepatic cancer in a Chinese populationMinghua Cui, Quanzhu Chen, Chaojun He, et al.
Cell Metabolism|April 9, 2019
Transmembrane 4 L Six Family Member 5 Senses Arginine for mTORC1 SignalingJae Woo Jung, Stephani Joy Y Macalino, Minghua Cui, et al.
Journal of Chemical Information and Modeling|March 14, 2025
Employing Automated Machine Learning (AutoML) Methods to Facilitate the In Silico ADMET Properties PredictionHerim Han, Bilal Shaker, Jin Hee Lee, et al.
Experimental Dermatology|March 27, 2015
Anti-angiogenic activity of thienopyridine derivative LCB03-0110 by targeting VEGFR-2 and JAK/STAT3 SignallingByung-Hak Kim, Yoonji Lee, Hyun Yoo, et al.
Bioorganic & Medicinal Chemistry|February 6, 2018
Potent human glutaminyl cyclase inhibitors as potential anti-Alzheimer's agents: Structure-activity relationship study of Arg-mimetic regionVan T H Ngo, Van-Hai Hoang, Phuong-Thao Tran, et al.
Bioorganic & Medicinal Chemistry|October 4, 2015
5-Lipoxygenase inhibitors suppress RANKL-induced osteoclast formation via NFATc1 expressionJu-Hee Kang, Zheng Ting, Mi-ran Moon, et al.
Bioorganic & Medicinal Chemistry|April 30, 2018
Structure-activity relationship investigation of Phe-Arg mimetic region of human glutaminyl cyclase inhibitorsVan T H Ngo, Van-Hai Hoang, Phuong-Thao Tran, et al.
Journal of Medicinal Chemistry|February 25, 2017
Discovery of Potent Human Glutaminyl Cyclase Inhibitors as Anti-Alzheimer's Agents Based on Rational DesignVan-Hai Hoang, Phuong-Thao Tran, Minghua Cui, et al.
Journal of Medicinal Chemistry|August 15, 2019
Discovery of Conformationally Restricted Human Glutaminyl Cyclase Inhibitors as Potent Anti-Alzheimer's Agents by Structure-Based DesignVan-Hai Hoang, Van T H Ngo, Minghua Cui, et al.
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