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A Hsu

Showing results (351-360 of 361) with videos related to

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Journal of Medicinal Chemistry|September 9, 2015
Identification of Substituted Naphthotriazolediones as Novel Tryptophan 2,3-Dioxygenase (TDO) Inhibitors through Structure-Based Virtual ScreeningJian-Sung Wu, Shu-Yu Lin, Fang-Yu Liao, et al.
Bioorganic & Medicinal Chemistry|April 27, 2013
Discovery of 3-phenyl-1H-5-pyrazolylamine derivatives containing a urea pharmacophore as potent and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3)Wen-Hsing Lin, John T-A Hsu, Shu-Yi Hsieh, et al.
Journal of Medicinal Chemistry|June 17, 2010
Fast-forwarding hit to lead: aurora and epidermal growth factor receptor kinase inhibitor lead identificationMohane Selvaraj Coumar, Chang-Ying Chu, Cheng-Wei Lin, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 24, 2013
Aurora kinase inhibitors reveal mechanisms of HURP in nucleation of centrosomal and kinetochore microtubulesJiun-Ming Wu, Chiung-Tong Chen, Mohane Selvaraj Coumar, et al.
Antimicrobial Agents and Chemotherapy|December 3, 1998
ABT-378, a highly potent inhibitor of the human immunodeficiency virus proteaseH L Sham, D J Kempf, A Molla, et al.
Communications Earth & Environment|March 18, 2025
Integrated fire management as an adaptation and mitigation strategy to altered fire regimesI Oliveras Menor, N Prat-Guitart, G L Spadoni, et al.
Journal of Medicinal Chemistry|October 22, 2010
Design and synthesis of tetrahydropyridothieno[2,3-d]pyrimidine scaffold based epidermal growth factor receptor (EGFR) kinase inhibitors: the role of side chain chirality and Michael acceptor group for maximal potencyChia-Hsien Wu, Mohane Selvaraj Coumar, Chang-Ying Chu, et al.
Oncotarget|November 19, 2016
Discovery of BPR1K871, a quinazoline based, multi-kinase inhibitor for the treatment of AML and solid tumors: Rational design, synthesis, in vitro and in vivo evaluationYung Chang Hsu, Mohane Selvaraj Coumar, Wen-Chieh Wang, et al.
Geroscience|January 25, 2020
Loss of vacuolar acidity results in iron-sulfur cluster defects and divergent homeostatic responses during aging in Saccharomyces cerevisiaeKenneth L Chen, Toby N Ven, Matthew M Crane, et al.
Applied Biochemistry and Biotechnology|November 16, 2013
Patents and literatureA Rembaum, R P Rohrbach, S Klose, et al.
Pageof 37

Showing results (351-360 of 361) with videos related to

Sort By:
Pageof 37
Journal of Medicinal Chemistry|September 9, 2015
Identification of Substituted Naphthotriazolediones as Novel Tryptophan 2,3-Dioxygenase (TDO) Inhibitors through Structure-Based Virtual ScreeningJian-Sung Wu, Shu-Yu Lin, Fang-Yu Liao, et al.
Bioorganic & Medicinal Chemistry|April 27, 2013
Discovery of 3-phenyl-1H-5-pyrazolylamine derivatives containing a urea pharmacophore as potent and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3)Wen-Hsing Lin, John T-A Hsu, Shu-Yi Hsieh, et al.
Journal of Medicinal Chemistry|June 17, 2010
Fast-forwarding hit to lead: aurora and epidermal growth factor receptor kinase inhibitor lead identificationMohane Selvaraj Coumar, Chang-Ying Chu, Cheng-Wei Lin, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 24, 2013
Aurora kinase inhibitors reveal mechanisms of HURP in nucleation of centrosomal and kinetochore microtubulesJiun-Ming Wu, Chiung-Tong Chen, Mohane Selvaraj Coumar, et al.
Antimicrobial Agents and Chemotherapy|December 3, 1998
ABT-378, a highly potent inhibitor of the human immunodeficiency virus proteaseH L Sham, D J Kempf, A Molla, et al.
Communications Earth & Environment|March 18, 2025
Integrated fire management as an adaptation and mitigation strategy to altered fire regimesI Oliveras Menor, N Prat-Guitart, G L Spadoni, et al.
Journal of Medicinal Chemistry|October 22, 2010
Design and synthesis of tetrahydropyridothieno[2,3-d]pyrimidine scaffold based epidermal growth factor receptor (EGFR) kinase inhibitors: the role of side chain chirality and Michael acceptor group for maximal potencyChia-Hsien Wu, Mohane Selvaraj Coumar, Chang-Ying Chu, et al.
Oncotarget|November 19, 2016
Discovery of BPR1K871, a quinazoline based, multi-kinase inhibitor for the treatment of AML and solid tumors: Rational design, synthesis, in vitro and in vivo evaluationYung Chang Hsu, Mohane Selvaraj Coumar, Wen-Chieh Wang, et al.
Geroscience|January 25, 2020
Loss of vacuolar acidity results in iron-sulfur cluster defects and divergent homeostatic responses during aging in Saccharomyces cerevisiaeKenneth L Chen, Toby N Ven, Matthew M Crane, et al.
Applied Biochemistry and Biotechnology|November 16, 2013
Patents and literatureA Rembaum, R P Rohrbach, S Klose, et al.
Pageof 37