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Dong Cheng

Showing results (611-620 of 625) with videos related to

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Journal of Medicinal Chemistry|August 15, 2022
Identification of Monosaccharide Derivatives as Potent, Selective, and Orally Bioavailable Inhibitors of Human and Mouse Galectin-3Chunjian Liu, Prasada Rao Jalagam, Jianxin Feng, et al.
Bioorganic & Medicinal Chemistry Letters|June 9, 2023
Discovery of novel pyridinones as MGAT2 inhibitors for the treatment of metabolic disordersFang Moore, Wei Wang, Guohua Zhao, et al.
World Journal of Gastroenterology|June 20, 2025
Evaluating log odds of positive lymph nodes as a prognostic tool in differentiated gastric cancer: A retrospective studyMing-Cong Deng, Ken Chen, Qi-Mei Bao, et al.
Cell Metabolism|November 2, 2022
MGAT2 inhibitor decreases liver fibrosis and inflammation in murine NASH models and reduces body weight in human adults with obesityDong Cheng, Bradley A Zinker, Yi Luo, et al.
Communications Medicine|October 25, 2023
Selective MCL-1 inhibitor ABBV-467 is efficacious in tumor models but is associated with cardiac troponin increases in patientsJunichiro Yuda, Christine Will, Darren C Phillips, et al.
Cancer Research|March 25, 2018
A Large-Scale, Exome-Wide Association Study of Han Chinese Women Identifies Three Novel Loci Predisposing to Breast CancerBo Zhang, Men-Yun Chen, Yu-Jun Shen, et al.
Journal of Medicinal Chemistry|September 19, 2023
Discovery of <b>12</b> (BMS-986172) as a Highly Potent MGAT2 Inhibitor that Achieved Targeted Efficacious Exposures at a Low Human Dose for the Treatment of Metabolic DisordersWei Meng, Robert Brigance, James Mignone, et al.
Molecular Cancer Therapeutics|May 5, 2017
Discovery and Characterization of Novel Nonsubstrate and Substrate NAMPT InhibitorsJulie L Wilsbacher, Min Cheng, Dong Cheng, et al.
Bioorganic & Medicinal Chemistry Letters|June 15, 2017
SAR and characterization of non-substrate isoindoline urea inhibitors of nicotinamide phosphoribosyltransferase (NAMPT)Michael L Curtin, H Robin Heyman, Richard F Clark, et al.
Journal of Medicinal Chemistry|October 6, 2021
Screening Hit to Clinical Candidate: Discovery of BMS-963272, a Potent, Selective MGAT2 Inhibitor for the Treatment of Metabolic DisordersHuji Turdi, Hannguang Chao, Jon J Hangeland, et al.
Pageof 63

Showing results (611-620 of 625) with videos related to

Sort By:
Pageof 63
Journal of Medicinal Chemistry|August 15, 2022
Identification of Monosaccharide Derivatives as Potent, Selective, and Orally Bioavailable Inhibitors of Human and Mouse Galectin-3Chunjian Liu, Prasada Rao Jalagam, Jianxin Feng, et al.
Bioorganic & Medicinal Chemistry Letters|June 9, 2023
Discovery of novel pyridinones as MGAT2 inhibitors for the treatment of metabolic disordersFang Moore, Wei Wang, Guohua Zhao, et al.
World Journal of Gastroenterology|June 20, 2025
Evaluating log odds of positive lymph nodes as a prognostic tool in differentiated gastric cancer: A retrospective studyMing-Cong Deng, Ken Chen, Qi-Mei Bao, et al.
Cell Metabolism|November 2, 2022
MGAT2 inhibitor decreases liver fibrosis and inflammation in murine NASH models and reduces body weight in human adults with obesityDong Cheng, Bradley A Zinker, Yi Luo, et al.
Communications Medicine|October 25, 2023
Selective MCL-1 inhibitor ABBV-467 is efficacious in tumor models but is associated with cardiac troponin increases in patientsJunichiro Yuda, Christine Will, Darren C Phillips, et al.
Cancer Research|March 25, 2018
A Large-Scale, Exome-Wide Association Study of Han Chinese Women Identifies Three Novel Loci Predisposing to Breast CancerBo Zhang, Men-Yun Chen, Yu-Jun Shen, et al.
Journal of Medicinal Chemistry|September 19, 2023
Discovery of <b>12</b> (BMS-986172) as a Highly Potent MGAT2 Inhibitor that Achieved Targeted Efficacious Exposures at a Low Human Dose for the Treatment of Metabolic DisordersWei Meng, Robert Brigance, James Mignone, et al.
Molecular Cancer Therapeutics|May 5, 2017
Discovery and Characterization of Novel Nonsubstrate and Substrate NAMPT InhibitorsJulie L Wilsbacher, Min Cheng, Dong Cheng, et al.
Bioorganic & Medicinal Chemistry Letters|June 15, 2017
SAR and characterization of non-substrate isoindoline urea inhibitors of nicotinamide phosphoribosyltransferase (NAMPT)Michael L Curtin, H Robin Heyman, Richard F Clark, et al.
Journal of Medicinal Chemistry|October 6, 2021
Screening Hit to Clinical Candidate: Discovery of BMS-963272, a Potent, Selective MGAT2 Inhibitor for the Treatment of Metabolic DisordersHuji Turdi, Hannguang Chao, Jon J Hangeland, et al.
Pageof 63