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L Meagher

Showing results (121-130 of 143) with videos related to

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Journal of the American Chemical Society|November 15, 2007
Design, synthesis, and characterization of a potent, nonpeptide, cell-permeable, bivalent Smac mimetic that concurrently targets both the BIR2 and BIR3 domains in XIAPHaiying Sun, Zaneta Nikolovska-Coleska, Jianfeng Lu, et al.
Scientific Reports|February 5, 2022
Genetic studies of fall armyworm indicate a new introduction into Africa and identify limits to its migratory behaviorRodney N Nagoshi, Georg Goergen, Djima Koffi, et al.
Journal of the American Chemical Society|February 7, 2013
Ordering a dynamic protein via a small-molecule stabilizerNingkun Wang, Chinmay Y Majmudar, William C Pomerantz, et al.
Journal of Medicinal Chemistry|January 2, 2025
Discovery of High-Affinity SMARCA2/4 Bromodomain Ligands and Development of Potent and Exceptionally Selective SMARCA2 PROTAC DegradersLingying Leng, Wenbin Tu, Lin Yang, et al.
Journal of Medicinal Chemistry|May 3, 2017
Structure-Based Discovery of 4-(6-Methoxy-2-methyl-4-(quinolin-4-yl)-9H-pyrimido[4,5-b]indol-7-yl)-3,5-dimethylisoxazole (CD161) as a Potent and Orally Bioavailable BET Bromodomain InhibitorYujun Zhao, Longchuan Bai, Liu Liu, et al.
Journal of Medicinal Chemistry|September 23, 2024
Discovery of AK-1690: A Potent and Highly Selective STAT6 PROTAC DegraderAtsunori Kaneshige, Yiqing Yang, Longchuan Bai, et al.
BMC Genomics|February 7, 2025
Genomic patterns of strain-specific genetic structure, linkage, and selection across fall armyworm populationsAshley E Tessnow, Rodney N Nagoshi, Robert L Meagher, et al.
Nature Chemical Biology|February 2, 2023
A selective small-molecule STAT5 PROTAC degrader capable of achieving tumor regression in vivoAtsunori Kaneshige, Longchuan Bai, Mi Wang, et al.
Journal of Medicinal Chemistry|November 7, 2024
Discovery of SD-436: A Potent, Highly Selective and Efficacious STAT3 PROTAC Degrader Capable of Achieving Complete and Long-Lasting Tumor RegressionRenqi Xu, Haibin Zhou, Longchuan Bai, et al.
Bioorganic & Medicinal Chemistry Letters|August 30, 2008
Discovery of amido-benzisoxazoles as potent c-Kit inhibitorsRoxanne K Kunz, Shannon Rumfelt, Ning Chen, et al.
Pageof 15

Showing results (121-130 of 143) with videos related to

Sort By:
Pageof 15
Journal of the American Chemical Society|November 15, 2007
Design, synthesis, and characterization of a potent, nonpeptide, cell-permeable, bivalent Smac mimetic that concurrently targets both the BIR2 and BIR3 domains in XIAPHaiying Sun, Zaneta Nikolovska-Coleska, Jianfeng Lu, et al.
Scientific Reports|February 5, 2022
Genetic studies of fall armyworm indicate a new introduction into Africa and identify limits to its migratory behaviorRodney N Nagoshi, Georg Goergen, Djima Koffi, et al.
Journal of the American Chemical Society|February 7, 2013
Ordering a dynamic protein via a small-molecule stabilizerNingkun Wang, Chinmay Y Majmudar, William C Pomerantz, et al.
Journal of Medicinal Chemistry|January 2, 2025
Discovery of High-Affinity SMARCA2/4 Bromodomain Ligands and Development of Potent and Exceptionally Selective SMARCA2 PROTAC DegradersLingying Leng, Wenbin Tu, Lin Yang, et al.
Journal of Medicinal Chemistry|May 3, 2017
Structure-Based Discovery of 4-(6-Methoxy-2-methyl-4-(quinolin-4-yl)-9H-pyrimido[4,5-b]indol-7-yl)-3,5-dimethylisoxazole (CD161) as a Potent and Orally Bioavailable BET Bromodomain InhibitorYujun Zhao, Longchuan Bai, Liu Liu, et al.
Journal of Medicinal Chemistry|September 23, 2024
Discovery of AK-1690: A Potent and Highly Selective STAT6 PROTAC DegraderAtsunori Kaneshige, Yiqing Yang, Longchuan Bai, et al.
BMC Genomics|February 7, 2025
Genomic patterns of strain-specific genetic structure, linkage, and selection across fall armyworm populationsAshley E Tessnow, Rodney N Nagoshi, Robert L Meagher, et al.
Nature Chemical Biology|February 2, 2023
A selective small-molecule STAT5 PROTAC degrader capable of achieving tumor regression in vivoAtsunori Kaneshige, Longchuan Bai, Mi Wang, et al.
Journal of Medicinal Chemistry|November 7, 2024
Discovery of SD-436: A Potent, Highly Selective and Efficacious STAT3 PROTAC Degrader Capable of Achieving Complete and Long-Lasting Tumor RegressionRenqi Xu, Haibin Zhou, Longchuan Bai, et al.
Bioorganic & Medicinal Chemistry Letters|August 30, 2008
Discovery of amido-benzisoxazoles as potent c-Kit inhibitorsRoxanne K Kunz, Shannon Rumfelt, Ning Chen, et al.
Pageof 15