Hans Bräuner-Osborne
Hans Bräuner-Osborne
Professor of Molecular Pharmacology, University of Copenhagen
Zweryfikowany adres z sund.ku.dk
Cytowane przez
Cytowane przez
The Concise Guide to PHARMACOLOGY 2019/20: G protein‐coupled receptors
SPH Alexander, A Christopoulos, AP Davenport, E Kelly, A Mathie, ...
British journal of pharmacology 176, S21-S141, 2019
Ligands for glutamate receptors: design and therapeutic prospects
H Bräuner-Osborne, J Egebjerg, EØ Nielsen, U Madsen, ...
Journal of medicinal chemistry 43 (14), 2609-2645, 2000
Extracellular Ca2+ is a danger signal activating the NLRP3 inflammasome through G protein-coupled calcium sensing receptors
M Rossol, M Pierer, N Raulien, D Quandt, U Meusch, K Rothe, K Schubert, ...
Nature communications 3 (1), 1329, 2012
The Concise Guide to PHARMACOLOGY 2021/22: G protein‐coupled receptors
SPH Alexander, A Christopoulos, AP Davenport, E Kelly, A Mathie, ...
British journal of pharmacology 178, S27-S156, 2021
Differential compartmentalization and distinct functions of GABAB receptor variants
R Vigot, S Barbieri, H Bräuner-Osborne, R Turecek, R Shigemoto, ...
Neuron 50 (4), 589-601, 2006
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
The concise guide to pharmacology 2017/18: overview
SPH Alexander, E Kelly, NV Marrion, JA Peters, E Faccenda, SD Harding, ...
British journal of pharmacology 174, S1-S16, 2017
The concise guide to PHARMACOLOGY 2015/16: Overview
SPH Alexander, E Kelly, N Marrion, JA Peters, HE Benson, E Faccenda, ...
British journal of pharmacology 172 (24), 5729-5743, 2015
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
Agonists and inverse agonists for the herpesvirus 8-encoded constitutively active seven-transmembrane oncogene product, ORF-74
MM Rosenkilde, TN Kledal, H Bräuner-Osborne, TW Schwartz
Journal of Biological Chemistry 274 (2), 956-961, 1999
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
The agonist-binding domain of the calcium-sensing receptor is located at the amino-terminal domain
H Bräuner-Osborne, AA Jensen, PO Sheppard, P O'Hara, ...
Journal of Biological Chemistry 274 (26), 18382-18386, 1999
Positive allosteric modulation of the human metabotropic glutamate receptor 4 (hmGluR4) by SIB‐1893 and MPEP
JM Mathiesen, N Svendsen, H Bräuner‐Osborne, C Thomsen, ...
British journal of pharmacology 138 (6), 1026-1030, 2003
Discovery of human signaling systems: pairing peptides to G protein-coupled receptors
SR Foster, AS Hauser, L Vedel, RT Strachan, XP Huang, AC Gavin, ...
Cell 179 (4), 895-908. e21, 2019
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
Real-time trafficking and signaling of the glucagon-like peptide-1 receptor
SN Roed, P Wismann, CR Underwood, N Kulahin, H Iversen, ...
Molecular and cellular endocrinology 382 (2), 938-949, 2014
Pharmacology of muscarinic acetylcholine receptor subtypes (m1–m5): high throughput assays in mammalian cells
H Bräuner-Osborne, MR Brann
European journal of pharmacology 295 (1), 93-102, 1996
Different domains of the glucagon and glucagon‐like peptide‐1 receptors provide the critical determinants of ligand selectivity
S Runge, BS Wulff, K Madsen, H Bräuner‐Osborne, LB Knudsen
British journal of pharmacology 138 (5), 787-794, 2003
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
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