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Naunyn-Schmiedeberg'S Archives of Pharmacology|March 10, 2004
Functional 5-HT receptors in human occipital arteryRaphaela Verheggen, Andreas Meier, Inga Werner, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 17, 2020
An inactive receptor-G protein complex maintains the dynamic range of agonist-induced signalingWonjo Jang, C Elizabeth Adams, Heng Liu, et al.
ACS Chemical Neuroscience|February 24, 2015
Downregulation of 5-HT7 Serotonin Receptors by the Atypical Antipsychotics Clozapine and Olanzapine. Role of Motifs in the C-Terminal Domain and Interaction with GASP-1Ornella Manfra, Kathleen Van Craenenbroeck, Kamila Skieterska, et al.
European Journal of Immunology|November 11, 2008
The heterotrimeric G-protein alpha-subunit Galphaq regulates TCR-mediated immune responses through an Lck-dependent pathwayJacob Ngai, Trond Methi, Kjetil Wessel Andressen, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 4, 2018
Preassociation between the 5-HT7 serotonin receptor and G protein Gs: molecular determinants and association with low potency activation of adenylyl cyclaseAndrea Hembre Ulsund, Marie Dahl, Thomas M Frimurer, et al.
British Journal of Pharmacology|September 27, 2016
Functional pharmacological characterization of SER100 in cardiovascular health and diseaseInmaculada C Villar, Kristen J Bubb, Amie J Moyes, et al.
Plos One|October 3, 2012
Retinoic acid signalling is activated in the postischemic heart and may influence remodellingDusan Bilbija, Fred Haugen, Julia Sagave, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|September 9, 2011
Agents increasing cyclic GMP amplify 5-HT4-elicited positive inotropic response in failing rat cardiac ventricleFaraz Afzal, Eirik Qvigstad, Jan Magnus Aronsen, et al.
European Journal of Medicinal Chemistry|May 29, 2013
Synthesis and pharmacological properties of a new hydrophilic and orally bioavailable 5-HT4 antagonistBjarne Brudeli, Lise Román Moltzau, Cam H T Nguyen, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 27, 2013
NSC23766, a widely used inhibitor of Rac1 activation, additionally acts as a competitive antagonist at muscarinic acetylcholine receptorsMagdolna Levay, Kurt Allen Krobert, Karola Wittig, et al.
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