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Biomed Research International|November 7, 2014
H-CRRETAWAC-OH, a lead structure for the development of radiotracer targeting integrin α5β1?Roland Haubner, Simone Maschauer, Jürgen Einsiedel, et al.
Nature Communications|July 27, 2016
Structure-guided development of heterodimer-selective GPCR ligandsHarald Hübner, Tamara Schellhorn, Marie Gienger, et al.
Journal of Medicinal Chemistry|July 18, 2009
Dopamine D2, D3, and D4 selective phenylpiperazines as molecular probes to explore the origins of subtype specific receptor bindingKatharina Ehrlich, Angela Götz, Stefan Bollinger, et al.
European Journal of Medicinal Chemistry|February 11, 2021
Dibenzodiazepinone-type muscarinic receptor antagonists conjugated to basic peptides: Impact of the linker moiety and unnatural amino acids on M<sub>2</sub>R selectivityCorinna G Weinhart, David Wifling, Maximilian F Schmidt, et al.
Pharmaceuticals (Basel, Switzerland)|April 19, 2014
In vivo monitoring of the antiangiogenic effect of neurotensin receptor-mediated radiotherapy by small-animal positron emission tomography: a pilot studySimone Maschauer, Tina Ruckdeschel, Philipp Tripal, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 10, 2014
Covalent agonists for studying G protein-coupled receptor activationDietmar Weichert, Andrew C Kruse, Aashish Manglik, et al.
Nature Communications|May 2, 2022
Activation and allosteric regulation of the orphan GPR88-Gi1 signaling complexGeng Chen, Jun Xu, Asuka Inoue, et al.
Journal of Medicinal Chemistry|February 27, 2023
Discovery of 2-Aminopyrimidines as Potent Agonists for the Bitter Taste Receptor TAS2R14Lukas Waterloo, Harald Hübner, Fabrizio Fierro, et al.
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