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Journal of Medicinal Chemistry|March 8, 2011
Design, synthesis, and structure-activity relationship exploration of 1-substituted 4-aroyl-3-hydroxy-5-phenyl-1H-pyrrol-2(5H)-one analogues as inhibitors of the annexin A2-S100A10 protein interactionTummala R K Reddy, Chan Li, Xiaoxia Guo, et al.The Journal of Biological Chemistry|November 24, 2004
UTP induces osteopontin expression through a coordinate action of NFkappaB, activator protein-1, and upstream stimulatory factor in arterial smooth muscle cellsMarie-Ange Renault, Sandra Jalvy, Mylène Potier, et al.Virology Journal|November 20, 2016
Annexin A2 antibodies but not inhibitors of the annexin A2 heterotetramer impair productive HIV-1 infection of macrophages in vitroAndrew W Woodham, Adriana M Sanna, Julia R Taylor, et al.European Journal of Pharmacology|December 6, 2005
Analysis of human Nav1.8 expressed in SH-SY5Y neuroblastoma cellsLodewijk V Dekker, Zoe Daniels, Caroline Hick, et al.ACS Omega|May 5, 2020
Use of BODIPY-Labeled ATP Analogues in the Development and Validation of a Fluorescence Polarization-Based Assay for Screening of Kinase InhibitorsBernardo Pereira Moreira, Tom Armstrong, Izabella Cristina Andrade Batista, et al.Acta Crystallographica. Section D, Structural Biology|June 18, 2019
Crystal structures of the recombinant β-factor XIIa protease with bound Thr-Arg and Pro-Arg substrate mimeticsMonika Pathak, Rosa Manna, Chan Li, et al.Breast Cancer Research : BCR|November 30, 2013
Critical research gaps and translational priorities for the successful prevention and treatment of breast cancerSuzanne A Eccles, Eric O Aboagye, Simak Ali, et al.Pageof 3