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Journal of Molecular Modeling|July 24, 2012
Structure-based design of nitrogen-linked macrocyclic kinase inhibitors leading to the clinical candidate SB1317/TG02, a potent inhibitor of cyclin dependant kinases (CDKs), Janus kinase 2 (JAK2), and Fms-like tyrosine kinase-3 (FLT3)Anders Poulsen, Anthony William, Stéphanie Blanchard, et al.Journal of Biomolecular Screening|November 14, 2006
SIRT1 modulating compounds from high-throughput screening as anti-inflammatory and insulin-sensitizing agentsVasantha M Nayagam, Xukun Wang, Yong Cheng Tan, et al.The Biochemical Journal|May 16, 2018
Structural and ligand-binding analysis of the YAP-binding domain of transcription factor TEAD4Yan Li, Shuang Liu, Elizabeth Yihui Ng, et al.Structure (London, England : 1993)|November 24, 2015
Targeting the Central Pocket in Human Transcription Factor TEAD as a Potential Cancer Therapeutic StrategyAjaybabu V Pobbati, Xiao Han, Alvin W Hung, et al.The Biochemical Journal|January 28, 2017
Discovery and characterisation of the automethylation properties of PRDM9Xiaoying Koh-Stenta, Anders Poulsen, Rong Li, et al.Critical Reviews in Food Science and Nutrition|June 6, 2025
Toward harmonizing protein data in food composition databases: evaluating perspectives, methods and implicationsLarissa E Pferdmenges, Paolo C Colombani, Monica Hauger Carlsen, et al.Biochemistry|November 29, 2014
Probing the binding mechanism of Mnk inhibitors by docking and molecular dynamics simulationsSrinivasaraghavan Kannan, Anders Poulsen, Hai Yan Yang, et al.Combinatorial Chemistry & High Throughput Screening|October 18, 2016
A Phenotypic Screen for Small-Molecule Inhibitors of Constitutively Active Mutant Thrombopoietin Receptor Implicated in Myeloproliferative NeoplasmsAnna Ngo, Ann Zhufang Koay, Christian Pecquet, et al.Journal of Computer-Aided Molecular Design|June 25, 2008
Structure-based design of Aurora A & B inhibitorsAnders Poulsen, Anthony William, Angeline Lee, et al.Bioorganic & Medicinal Chemistry Letters|May 18, 2012
Thieno[3,2-d]pyrimidin-4(3H)-one derivatives as PDK1 inhibitors discovered by fragment-based screeningAngeline C-H Lee, Pondy Murugappan Ramanujulu, Anders Poulsen, et al.Pageof 7