Publications by Kjetil Wessel Andressen
24 publications found
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Discovery and pharmacological profile of new hydrophilic 5-HT4 receptor antagonists
Bioorg. Med. Chem. Lett., 24 (18), 4598-4602
DOI 10.1016/j.bmcl.2014.06.083 -
Synthesis and pharmacological properties of novel hydrophilic 5-HT4 receptor antagonists
Bioorg. Med. Chem., 18 (24), 8600-8613
DOI 10.1016/j.bmc.2010.10.011 -
An inactive receptor-G protein complex maintains the dynamic range of agonist-induced signaling
Proc. Natl. Acad. Sci. U. S. A., 117 (48), 30755-30762
DOI 10.1073/pnas.2010801117 -
The atypical antipsychotics clozapine and olanzapine promote down-regulation and display functional selectivity at human 5-HT7 receptors
Br. J. Pharmacol., 172 (15), 3846-3860
DOI 10.1111/bph.13169 -
Acidic biphenyl derivatives: Synthesis and biological activity of a new series of potent 5-HT4 receptor antagonists
Bioorg. Med. Chem., 21 (22), 7134-7145
DOI 10.1016/j.bmc.2013.09.004 -
Cloning, genomic organization and functionality of 5-HT7 receptor splice variants from mouse brain
Gene, 426 (1-2), 23-31
DOI 10.1016/j.gene.2008.08.011 -
Related GPCRs couple differently to G(s): preassociation between G protein and 5-HT7 serotonin receptor reveals movement of Gas upon receptor activation
Faseb J., 32 (2), 1059-1069
DOI 10.1096/fj.201700486R -
The Inotropic Effect of the Active Metabolite of Levosimendan, OR-1896, Is Mediated through Inhibition of PDE3 in Rat Ventricular Myocardium
PLoS One, 10 (3), e0115547
DOI 10.1371/journal.pone.0115547 -
Biochemical and pharmacological study of N-linked glycosylation of the human serotonin 5-HT7(a) receptor
FEBS J., 279 (11), 1994-2003
DOI 10.1111/j.1742-4658.2012.08581.x -
Exercise Training Stabilizes RyR2-Dependent Ca2+ Release in Post-infarction Heart Failure
Front. Cardiovasc. Med., 7, 623922
DOI 10.3389/fcvm.2020.623922 -
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-1
ACS Chem. Neurosci., 6 (7), 1206-1218
DOI 10.1021/cn500339p -
Synthesis and in vitro evaluation of small-molecule [F-18] labeled gonadotropin-releasing hormone (GnRH) receptor antagonists as potential PET imaging agents for GnRH receptor expression
Bioorg. Med. Chem. Lett., 24 (7), 1846-1850
DOI 10.1016/j.bmcl.2014.02.002 -
5-HT4-elicited positive inotropic response is mediated by cAMP and regulated by PDE3 in failing rat and human cardiac ventricles
Br. J. Pharmacol., 155 (7), 1005-1014
DOI 10.1038/bjp.2008.339 -
Preassociation between the 5-HT7 serotonin receptor and G protein G(s): molecular determinants and association with low potency activation of adenylyl cyclase
Faseb J., 33 (3), 3870-3886
DOI 10.1096/fj.201800805RR -
Radiosynthesis of high affinity fluorine-18 labeled GnRH peptide analogues: in vitro studies and in vivo assessment of brain uptake in rats
MedChemComm, 6 (4), 708-714
DOI 10.1039/c4md00486h -
Synthesis and pharmacological properties of a new hydrophilic and orally bioavailable 5-HT4 antagonist
Eur. J. Med. Chem., 64, 629-637
DOI 10.1016/j.ejmech.2013.03.060 -
Brain penetrant small molecule F-18-GnRH receptor (GnRH-R) antagonists: Synthesis and preliminary positron emission tomography imaging in rats
Nucl. Med. Biol., 43 (8), 478-489
DOI 10.1016/j.nucmedbio.2016.05.003 -
Disheveled regulates precoupling of heterotrimeric G proteins to Frizzled 6
Faseb J., 28 (5), 2293-2305
DOI 10.1096/fj.13-246363 -
The heterotrimeric G-protein alpha-subunit G alpha q regulates TCR-mediated immune responses through an Lck-dependent pathway
Eur. J. Immunol., 38 (11), 3208-3218
DOI 10.1002/eji.200838195 -
FRET-based cyclic GMP biosensors measure low cGMP concentrations in cardiomyocytes and neurons
Commun. Biol., 2, 394
DOI 10.1038/s42003-019-0641-x -
Identification of essential residues for binding and activation in the human 5-HT7(a) serotonin receptor by molecular modeling and site-directed mutagenesis
Front. Behav. Neurosci., 9, 92
DOI 10.3389/fnbeh.2015.00092 -
The serotonin 5-HT7 receptors: two decades of research
Exp. Brain Res., 230 (4), 555-568
DOI 10.1007/s00221-013-3694-y -
Substrate specificities of G protein-coupled receptor kinase-2 and -3 at cardiac myocyte receptors provide basis for distinct roles in regulation of myocardial function
Mol. Pharmacol., 72 (3), 582-591
DOI 10.1124/mol.107.035766 -
PDE3 inhibition by C-type natriuretic peptide-induced cGMP enhances cAMP-mediated signaling in both non-failing and failing hearts
Eur. J. Pharmacol., 812, 174-183
DOI 10.1016/j.ejphar.2017.07.014