| Structure, pharmacology and therapeutic prospects of family C G-protein coupled receptors H Brauner-Osborne, P Wellendorph, AA Jensen Current drug targets 8 (1), 169-184, 2007 | 333 | 2007 |
| Deorphanization of GPRC6A: a promiscuous L-α-amino acid receptor with preference for basic amino acids P Wellendorph, KB Hansen, A Balsgaard, JR Greenwood, J Egebjerg, ... Molecular pharmacology 67 (3), 589-597, 2005 | 242 | 2005 |
| Specific γ‐hydroxybutyrate‐binding sites but loss of pharmacological effects of γ‐hydroxybutyrate in GABAB(1)‐deficient mice K Kaupmann, JF Cryan, P Wellendorph, C Mombereau, G Sansig, ... European Journal of Neuroscience 18 (10), 2722-2730, 2003 | 224 | 2003 |
| Molecular cloning, expression, and sequence analysis of GPRC6A, a novel family C G-protein-coupled receptor P Wellendorph, H Bräuner-Osborne Gene 335, 37-46, 2004 | 200 | 2004 |
| Molecular pharmacology of promiscuous seven transmembrane receptors sensing organic nutrients P Wellendorph, LD Johansen, H Bräuner-Osborne Molecular pharmacology 76 (3), 453-465, 2009 | 182 | 2009 |
| Molecular basis for amino acid sensing by family CG‐protein‐coupled receptors P Wellendorph, H Bräuner‐Osborne British journal of pharmacology 156 (6), 869-884, 2009 | 143 | 2009 |
| Molecular cloning and pharmacology of functionally distinct isoforms of the human histamine H3 receptor P Wellendorph, MW Goodman, ES Burstein, NR Nash, MR Brann, ... Neuropharmacology 42 (7), 929-940, 2002 | 140 | 2002 |
| GHB receptor targets in the CNS: focus on high-affinity binding sites T Bay, LF Eghorn, AB Klein, P Wellendorph Biochemical pharmacology 87 (2), 220-228, 2014 | 126 | 2014 |
| The GPCR, class C, group 6, subtype A (GPRC6A) receptor: from cloning to physiological function C Clemmensen, S Smajilovic, P Wellendorph, H Bräuner‐Osborne British journal of pharmacology 171 (5), 1129-1141, 2014 | 123 | 2014 |
| α4βδ GABAA receptors are high-affinity targets for γ-hydroxybutyric acid (GHB) N Absalom, LF Eghorn, IS Villumsen, N Karim, T Bay, JV Olsen, ... Proceedings of the National Academy of Sciences 109 (33), 13404-13409, 2012 | 114 | 2012 |
| Pharmacological characterization of mouse GPRC6A, an L‐α‐amino‐acid receptor modulated by divalent cations B Christiansen, KB Hansen, P Wellendorph, H Bräuner‐Osborne British journal of pharmacology 150 (6), 798-807, 2007 | 100 | 2007 |
| Potency of GABA at human recombinant GABAA receptors expressed in Xenopus oocytes: a mini review N Karim, P Wellendorph, N Absalom, GAR Johnston, JR Hanrahan, ... Amino acids 44, 1139-1149, 2013 | 83 | 2013 |
| No evidence for a bone phenotype in GPRC6A knockout mice under normal physiological conditions P Wellendorph, LD Johansen, AA Jensen, E Casanova, M Gassmann, ... J Mol Endocrinol 42 (3), 215-23, 2009 | 81 | 2009 |
| Delineation of the GPRC6A receptor signaling pathways using a mammalian cell line stably expressing the receptor SE Jacobsen, L Nørskov-Lauritsen, ARB Thomsen, S Smajilovic, ... Journal of pharmacology and experimental therapeutics 347 (2), 298-309, 2013 | 78 | 2013 |
| The rat GPRC6A: cloning and characterization P Wellendorph, N Burhenne, B Christiansen, B Walter, H Schmale, ... Gene 396 (2), 257-267, 2007 | 70 | 2007 |
| Design, Synthesis, and Pharmacological Characterization of N-and O-Substituted 5, 6, 7, 8-Tetrahydro-4 H-isoxazolo [4, 5-d] azepin-3-ol Analogues: Novel 5-HT2A/5-HT2C Receptor … AA Jensen, N Plath, MHF Pedersen, V Isberg, J Krall, P Wellendorph, ... Journal of Medicinal Chemistry 56 (3), 1211-1227, 2013 | 67 | 2013 |
| The l-α-amino acid receptor GPRC6A is expressed in the islets of Langerhans but is not involved in l-arginine-induced insulin release S Smajilovic, C Clemmensen, LD Johansen, P Wellendorph, JJ Holst, ... Amino acids 44, 383-390, 2013 | 62 | 2013 |
| (1S, 3S)-3-Amino-4-difluoromethylenyl-1-cyclopentanoic Acid (CPP-115), a Potent γ-Aminobutyric Acid Aminotransferase Inactivator for the Treatment of Cocaine … Y Pan, MR Gerasimov, T Kvist, P Wellendorph, KK Madsen, E Pera, H Lee, ... Journal of medicinal chemistry 55 (1), 357-366, 2012 | 56 | 2012 |
| Novel cyclic γ-hydroxybutyrate (GHB) analogs with high affinity and stereoselectivity of binding to GHB sites in rat brain P Wellendorph, S Høg, JR Greenwood, A de Lichtenberg, B Nielsen, ... Journal of Pharmacology and Experimental Therapeutics 315 (1), 346-351, 2005 | 54 | 2005 |
| 3-Hydroxy-2′-methoxy-6-methylflavone: A potent anxiolytic with a unique selectivity profile at GABAA receptor subtypes N Karim, N Gavande, P Wellendorph, GAR Johnston, JR Hanrahan, ... Biochemical Pharmacology 82 (12), 1971-1983, 2011 | 52 | 2011 |
Hans Bräuner-OsborneProfessor of Molecular Pharmacology, University of CopenhagenVerifierad e-postadress på sund.ku.dk