Hans Bräuner

Prodekan for forskning

Fakultetsservice
Blegdamsvej 3
2200 København N.
- hans.brauner@sund.ku.dk
- https://sund.ku.dk/
Telefon: +45 35 33 44 69

ORCID: 0000-0001-9495-7388

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2017
Udgivet
THE CONCISE GUIDE TO PHARMACOLOGY 2017/18: Overview
CGTP Collaborators, C. C., dec. 2017, I: British Journal of Pharmacology. 174, s. S1-S16
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
Applying label-free dynamic mass redistribution assay for studying endogenous FPR1 receptor signalling in human neutrophils
Christensen, H. B., Gloriam, David E., Pedersen, D. S., Cowland, J. B., Borregaard, N. & Bräuner, Hans, 15 jul. 2017, I: Journal of Pharmacological and Toxicological Methods. 88, Pt 1, s. 72-78 7 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
Robust GLP-1 secretion by basic L-amino acids does not require the GPRC6A receptor
Clemmensen, Christoffer, Jørgensen, C. V., Smajilovic, S. & Bräuner, Hans, 2017, I: Diabetes, Obesity and Metabolism. 19, 4, s. 599-603
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
Investigating Internalization and Intracellular Trafficking of GPCRs: New Techniques and Real-Time Experimental Approaches
Foster, S. R. & Bräuner, Hans, 11 okt. 2017, Handbook of Experimental Pharmacology. Springer, Bind 245. s. 41-61 (Handbook of Experimental Pharmacology).
Publikation: Bidrag til bog/antologi/rapport › Bidrag til bog/antologi › Forskning › fagfællebedømt
Udgivet
Identification of Histamine H3 Receptor Ligands Using a New Crystal Structure Fragment-based Method
Frandsen, I. O., Boesgaard, M. W., Fidom, K., Hauser, Alexander Sebastian, Isberg, V., Bräuner, Hans, Wellendorph, Petrine & Gloriam, David E., 6 jul. 2017, I: Scientific Reports. 7, 1, 10 s., 4829.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
Structural insight to mutation effects uncover a common allosteric site in class C GPCRs
Harpsøe, Kasper, Boesgaard, M. W., Munk, C., Bräuner, Hans & Gloriam, David E., 2017, I: Bioinformatics (Oxford, England). 33, 8, s. 1116-1120 5 s., btw784.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
Investigating the molecular mechanism of positive and negative allosteric modulators in the calcium-sensing receptor dimer
Jacobsen, S. E., Gether, Ulrik & Bräuner, Hans, 2017, I: Scientific Reports. 7, 14 s., 46355.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
The GPRC6A Receptor displays Constitutive Internalization and Sorting to the Slow Recycling Pathway
Jacobsen, S. E., Ammendrup-Johnsen, I., Jansen, A. M., Gether, Ulrik, Madsen, Kenneth Lindegaard & Bräuner, Hans, 2017, I: The Journal of Biological Chemistry. 292, 17, s. 6910-6926
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
Detailed characterization of the in vitro pharmacological and pharmacokinetic properties of N-(2-hydroxybenzyl)-2,5-dimethoxy-4-cyanophenylethylamine (25CN-NBOH), a highly selective and brain-penetrant 5-HT2A receptor agonist
Jensen, Anders A., McCorvy, J. D., Petersen, S. L., Bundgaard, C., Liebscher, G., Kenakin, T. P., Bräuner, Hans, Kehler, J. & Kristensen, Jesper Langgaard, 2017, I: Journal of Pharmacology and Experimental Therapeutics. 361, 3, s. 441-453
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Udgivet
The orphan G protein-coupled receptor GPR139 is activated by the peptides: Adrenocorticotropic hormone (ACTH), α-, and β-melanocyte stimulating hormone (α-MSH, and β-MSH), and the conserved core motif HFRW
Jensen, A. C. N., Shehata, M. A., Hauser, Alexander Sebastian, Isberg, V., Mokrosinski, J., Farooqi, I. S., Pedersen, D. S., Gloriam, David E. & Bräuner, Hans, 1 jan. 2017, I: Neurochemistry International. 102, s. 105-113
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

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ID: 1302910

Forskning

Hans Bräuner

Fakultetsservice

THE CONCISE GUIDE TO PHARMACOLOGY 2017/18: Overview

Applying label-free dynamic mass redistribution assay for studying endogenous FPR1 receptor signalling in human neutrophils

Robust GLP-1 secretion by basic L-amino acids does not require the GPRC6A receptor

Investigating Internalization and Intracellular Trafficking of GPCRs: New Techniques and Real-Time Experimental Approaches

Identification of Histamine H3 Receptor Ligands Using a New Crystal Structure Fragment-based Method

Structural insight to mutation effects uncover a common allosteric site in class C GPCRs

Investigating the molecular mechanism of positive and negative allosteric modulators in the calcium-sensing receptor dimer

The GPRC6A Receptor displays Constitutive Internalization and Sorting to the Slow Recycling Pathway

Detailed characterization of the in vitro pharmacological and pharmacokinetic properties of N-(2-hydroxybenzyl)-2,5-dimethoxy-4-cyanophenylethylamine (25CN-NBOH), a highly selective and brain-penetrant 5-HT2A receptor agonist

The orphan G protein-coupled receptor GPR139 is activated by the peptides: Adrenocorticotropic hormone (ACTH), α-, and β-melanocyte stimulating hormone (α-MSH, and β-MSH), and the conserved core motif HFRW

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