Veröffentlichungswege
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- Universität Regensburg (10)
- Chemie und Pharmazie (10)
- Institut für Pharmazie (10)
- Lehrstuhl Pharmazeutische / Medizinische Chemie II (Prof. Buschauer) (10)
- Institut für Pharmazie (10)
- Chemie und Pharmazie (10)
Gruppieren nach: Datum | Autoren | Institutionen | Titel eines Journals oder einer Zeitschrift | Dokumentenart | Keine Gruppierung
Anzahl der Einträge in dieser Kategorie: 10.
2023
Hoffelner, Beate Sandra, Andreev, Stanislav
, Plank, Nicole und Koch, Pierre
(2023)
Photocaging of Pyridinylimidazole-Based Covalent JNK3 Inhibitors Affords Spatiotemporal Control of the Binding Affinity in Live Cells.
Pharmaceuticals 16 (2), S. 264.
2021
Höring, Carina
, Conrad, Marcus, Söldner, Christian A.
, Wang, Jinan
, Sticht, Heinrich
, Strasser, Andrea und Miao, Yinglong
(2021)
Specific Engineered G Protein Coupling to Histamine Receptors Revealed from Cellular Assay Experiments and Accelerated Molecular Dynamics Simulations.
International Journal of Molecular Sciences 22 (18), S. 1-21.
2020
Höring, Carina
, Seibel, Ulla
, Tropmann, Katharina, Grätz, Lukas
, Mönnich, Denise
, Pitzl, Sebastian, Bernhardt, Günther
, Pockes, Steffen
und Strasser, Andrea
(2020)
A Dynamic, Split-Luciferase-Based Mini-G Protein Sensor to Functionally Characterize Ligands at All Four Histamine Receptor Subtypes.
International Journal of Molecular Sciences 21 (22), S. 8440.
Forster, Lisa
, Grätz, Lukas, Mönnich, Denise, Bernhardt, Günther und Pockes, Steffen
(2020)
A Split Luciferase Complementation Assay for the Quantification of β-Arrestin2 Recruitment to Dopamine D2-Like Receptors.
International Journal of Molecular Sciences 21 (17), S. 6103.
2018
Littmann, Timo, Ozawa, Takeaki, Hoffmann, Carsten, Buschauer, Armin und Bernhardt, Günther
(2018)
A split luciferase-based probe for quantitative proximal determination of Gαq signalling in live cells.
Scientific Reports 8 (17179), S. 1-10.
2015
Wifling, David
, Bernhardt, Günther, Dove, Stefan und Buschauer, Armin
(2015)
The extracellular loop 2 (ECL2) of the human histamine H4 receptor substantially contributes to ligand binding and constitutive activity.
PLoS One 10 (1), S. 1-14.
Huber, Stefan, Huettner, Johannes Philip, Hacker, Kristina, Bernhardt, Günther, König, Jörg
und Buschauer, Armin
(2015)
Esters of bendamustine are by far more potent cytotoxic agents than the parent compound against human sarcoma and carcinoma cells.
PLoS One 10 (7), PLoSe0133743.
2014
Wittmann, Hans-Joachim, Seifert, Roland und Strasser, Andrea
(2014)
Mathematical analysis of the sodium sensitivity of the human histamine H3 receptor.
In silico pharmacology 2.
2013
Nordemann, Uwe, Wifling, David
, Schnell, David, Bernhardt, Günther, Stark, Holger
, Seifert, Roland und Buschauer, Armin
(2013)
Luciferase reporter gene assay on human, murine and rat histamine H4 receptor orthologs: correlations and discrepancies between distal and proximal readouts.
PLoS One 8 (9), e73961.
2012
Memminger, Martin, Keller, Max, Lopuch, Miroslaw, Pop, Nathalie, Bernhardt, Günther, von Angerer, Erwin und Buschauer, Armin
(2012)
The Neuropeptide Y Y1 receptor: a diagnostic marker? Expression in MCF-7 breast cancer cells is down-regulated by antiestrogens in vitro and in xenografts.
PLoS ONE 7 (12), e51032.
