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Scientific Reports|December 7, 2017
Na+ entry through heteromeric TRPC4/C1 channels mediates (-)Englerin A-induced cytotoxicity in synovial sarcoma cellsKatsuhiko Muraki, Kaori Ohnishi, Akiho Takezawa, et al.ACS Chemical Biology|April 17, 2018
Identification of Noncatalytic Lysine Residues from Allosteric Circuits via Covalent ProbesJens Bongard, Marian Lorenz, Ingrid R Vetter, et al.Journal of Medicinal Chemistry|July 11, 2018
Optimizing a Weakly Binding Fragment into a Potent RORγt Inverse Agonist with Efficacy in an in Vivo Inflammation ModelDavid A Carcache, Anna Vulpetti, Joerg Kallen, et al.JCI Insight|March 15, 2017
Retinoic-acid-orphan-receptor-C inhibition suppresses Th17 cells and induces thymic aberrationsChristine Guntermann, Alessandro Piaia, Marie-Laure Hamel, et al.Journal of Immunology (Baltimore, Md. : 1950)|February 23, 2008
Neutropenia with impaired immune response to Streptococcus pneumoniae in ceramide kinase-deficient miceChristine Graf, Barbara Zemann, Philipp Rovina, et al.Chemmedchem|April 5, 2019
Chemical Validation of DegS As a Target for the Development of Antibiotics with a Novel Mode of ActionJens Bongard, Anna Laura Schmitz, Alex Wolf, et al.Journal of Medicinal Chemistry|November 16, 2019
Structure-Based and Property-Driven Optimization of N-Aryl Imidazoles toward Potent and Selective Oral RORγt InhibitorsKlemens Hoegenauer, Joerg Kallen, Eloísa Jiménez-Núñez, et al.Scientific Reports|October 21, 2017
Feasibility and physiological relevance of designing highly potent aminopeptidase-sparing leukotriene A4 hydrolase inhibitorsShin Numao, Franziska Hasler, Claire Laguerre, et al.Circulation Research|July 2, 2015
Sphingosine 1-Phosphate Produced by Sphingosine Kinase 2 Intrinsically Controls Platelet Aggregation In Vitro and In VivoNicole Urtz, Florian Gaertner, Marie-Luise von Bruehl, et al.Nature Communications|April 21, 2016
Identification of pyrazolopyridazinones as PDEδ inhibitorsBjörn Papke, Sandip Murarka, Holger A Vogel, et al.Pageof 11