Petrine Wellendorph
Cytowane przez
Cytowane przez
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
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
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
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
Molecular pharmacology of promiscuous seven transmembrane receptors sensing organic nutrients
P Wellendorph, LD Johansen, H Bräuner-Osborne
Molecular pharmacology 76 (3), 453-465, 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
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
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
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
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
Pharmacological characterization of mouse GPRC6A, an Lα‐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
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
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
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
The rat GPRC6A: cloning and characterization
P Wellendorph, N Burhenne, B Christiansen, B Walter, H Schmale, ...
Gene 396 (2), 257-267, 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
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
(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
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
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
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