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Nature Microbiology|July 15, 2020
Targeting the trypanosome kinetochore with CLK1 protein kinase inhibitorsManuel Saldivia, Eric Fang, Xiaolei Ma, et al.Journal of the American Chemical Society|December 9, 2022
An Activity-Based Oxaziridine Platform for Identifying and Developing Covalent Ligands for Functional Allosteric Methionine Sites: Redox-Dependent Inhibition of Cyclin-Dependent Kinase 4Angel Gonzalez-Valero, Audrey G Reeves, Annika C S Page, et al.Journal of Medicinal Chemistry|September 27, 2024
Identification of Potent, Broad-Spectrum Coronavirus Main Protease Inhibitors for Pandemic PreparednessDavid T Barkan, Keira Garland, Lei Zhang, et al.Journal of Medicinal Chemistry|October 11, 2017
Synthesis, Binding Mode, and Antihyperglycemic Activity of Potent and Selective (5-Imidazol-2-yl-4-phenylpyrimidin-2-yl)[2-(2-pyridylamino)ethyl]amine Inhibitors of Glycogen Synthase Kinase 3Allan S Wagman, Rustum S Boyce, Sean P Brown, et al.Genome Research|December 14, 2005
The Oryza bacterial artificial chromosome library resource: construction and analysis of 12 deep-coverage large-insert BAC libraries that represent the 10 genome types of the genus OryzaJetty S S Ammiraju, Meizhong Luo, José L Goicoechea, et al.Plos One|April 7, 2017
Inhibition of prenylated KRAS in a lipid environmentJohanna M Jansen, Charles Wartchow, Wolfgang Jahnke, et al.Journal of Medicinal Chemistry|March 1, 2022
Discovery and Preclinical Pharmacology of INE963, a Potent and Fast-Acting Blood-Stage Antimalarial with a High Barrier to Resistance and Potential for Single-Dose Cures in Uncomplicated MalariaBenjamin R Taft, Fumiaki Yokokawa, Tom Kirrane, et al.Analytical Biochemistry|January 10, 2009
A global benchmark study using affinity-based biosensorsRebecca L Rich, Giuseppe A Papalia, Peter J Flynn, et al.Pageof 3