Publikationen von 0000-0002-7905-4276
(ORCID: 0000-0002-7905-4276)

Werner, Kristin, Kälble, Solveig, Wolter, Sabine, Schneider, Erich H. , Buschauer, Armin, Neumann, Detlef und Seifert, Roland (2015) Flow cytometric analysis with a fluorescent formyl peptide receptor ligand as a new method to study the pharmacological profile of the histamine H2-receptor. Naunyn Schmiedebergs Archives of Pharmacology 388 (10), S. 1039-1052. Volltext nicht vorhanden.

Schnell, David, Brunskole, Irena, Ladova, Katerina, Schneider, Erich H. , Igel, Patrick, Dove, Stefan, Buschauer, Armin und Seifert, Roland (2011) Expression and functional properties of canine, rat and murine histamine H4-receptors in Sf9 insect cells. Naunyn-Schmiedeberg's Archives of Pharmacology 383 (5), S. 457-470. Volltext nicht vorhanden.

Seifert, Roland, Schneider, Erich H. , Dove, Stefan, Brunskole, Irena, Neumann, Detlef , Strasser, Andrea und Buschauer, Armin (2011) Paradoxical stimulatory effects of the “standard” histamine H4-receptor antagonist JNJ7777120: The H4-receptor joins the club of 7TM receptors exhibiting functional selectivity. Molecular Pharmacology 79 (4), S. 631-638. Volltext nicht vorhanden.

Geiger, Sarah, Nickl, Kathrin, Schneider, Erich H. , Seifert, Roland und Heilmann, Jörg (2010) Establishment of recombinant cannabinoid receptor assays and characterization of several natural and synthetic ligands. Naunyn-Schmiedeberg's Archives of Pharmacology 382 (2), S. 177-191. Volltext nicht vorhanden.

Sander, Kerstin, Kottke, Tim, Hoffend, Claas, Walter, Miriam, Weizel, Lilia, Camelin, Jean-Claude, Ligneau, Xavier, Schneider, Erich H. , Seifert, Roland, Schwartz, Jean-Charles und Stark, Holger (2010) First Metal-Containing Histamine H3 Receptor Ligands. Organic Letters 12 (11), S. 2578-2581. Volltext nicht vorhanden.

Schneider, Erich , Schnell, David, Strasser, Andrea, Dove, Stefan und Seifert, Roland (2010) Impact of the DRY motif and the missing "ionic lock" on constitutive activity and G-protein coupling of the human histamine H4 receptor. J Pharmacol Exp Ther : The journal of pharmacology and experimental therapeutics 333 (2), S. 382-392. Volltext nicht vorhanden.

Schneider, Erich H. , Strasser, Andrea, Thurmond, Robin L. und Seifert, Roland (2010) Structural Requirements for Inverse Agonism and Neutral Antagonism of Indole-, Benzimidazole-, and Thienopyrrole-Derived Histamine H4 Receptor Ligands. Journal of Pharmacology and Experimental Therapeutics 334 (2), S. 513-521. Volltext nicht vorhanden.

Igel, Patrick, Schneider, Erich , Schnell, David, Elz, Sigurd, Seifert, Roland und Buschauer, Armin (2009) N(G)-Acylated imidazolylpropylguanidines as potent histamine H4 receptor agonists: selectivity by variation of the N(G)-substituent. Journal of Medicinal Chemistry 52 (8), S. 2623-2627. Volltext nicht vorhanden.

Sander, Kerstin, Kottke, Tim, Tanrikulu, Yusuf, Proschak, Ewgenij, Weizel, Lilia, Schneider, Erich H. , Seifert, Roland, Schneider, Gisbert und Stark, Holger (2009) 2,4-Diaminopyrimidines as histamine H4 receptor ligands—Scaffold optimization and pharmacological characterization. Bioorganic & Medicinal Chemistry 17 (20), S. 7186-7196. Volltext nicht vorhanden.

Schneider, Erich H. , Schnell, David, Papa, Dan und Seifert, Roland (2009) High Constitutive Activity and a G-Protein-Independent High-Affinity State of the Human Histamine H4-Receptor. Biochemistry 48 (6), S. 1424-1438. Volltext nicht vorhanden.

Schneider, Erich H. und Seifert, Roland (2009) Histamine H4 receptor–RGS fusion proteins expressed in Sf9 insect cells: A sensitive and reliable approach for the functional characterization of histamine H4 receptor ligands. Biochemical Pharmacology 78 (6), S. 607-616. Volltext nicht vorhanden.

Tanrikulu, Yusuf, Proschak, Ewgenij, Werner, Tim, Geppert, Tim, Todoroff, Nickolay, Klenner, Alexander, Kottke, Tim, Sander, Kerstin, Schneider, Erich , Seifert, Roland, Stark, Holger , Clark, Timothy und Schneider, Gisbert (2009) Homology Model Adjustment and Ligand Screening with a Pseudoreceptor of the Human Histamine H4 Receptor. ChemMedChem 4 (5), S. 820-827. Volltext nicht vorhanden.

Ghorai, Prasanta, Kraus, Anja, Keller, Max, Götte, Carsten, Igel, Patrick, Schneider, Erich , Schnell, David, Bernhardt, Günther, Dove, Stefan, Zabel, Manfred, Elz, Sigurd, Seifert, Roland und Buschauer, Armin (2008) Acylguanidines as bioisosteres of guanidines: N(G)-acylated imidazolylpropylguanidines, a new class of histamine H2 receptor agonists. Journal of Medicinal Chemistry 51 (22), S. 7193-7204. Volltext nicht vorhanden.

Ziemek, Ralf, Schneider, Erich , Kraus, Anja, Cabrele, Chiara , Beck-Sickinger, Annette G., Bernhardt, Günther und Buschauer, Armin (2007) Determination of affinity and activity of ligands at the human neuropeptide Y Y4 receptor by flow cytometry and aequorin luminescence. Journal of Receptors and Signal Transduction 27 (4), S. 217-233. Volltext nicht vorhanden.

Schneider, Erich , Keller, Max, Brennauer, Albert, Hoefelschweiger, Bianca K., Gross, Dietmar, Wolfbeis, Otto S. , Bernhardt, Günther und Buschauer, Armin (2007) Synthesis and Characterization of the First Fluorescent Nonpeptide NPY Y1 Receptor Antagonist. ChemBioChem 8 (16), S. 1981-1988. Zugang zum Volltext eingeschränkt.

Schneider, Erich , Mayer, Matthias, Ziemek, Ralf, Li, Liantao, Hutzler, Christoph , Bernhardt, Günther und Buschauer, Armin (2006) A Simple and Powerful Flow Cytometric Method for the Simultaneous Determination of Multiple Parameters at G-Protein-coupled Receptor Subtypes. ChemBioChem 7 (9), S. 1400-1409. Volltext nicht vorhanden.

Xie, Sheng-Xue, Petrache, Georgiana, Schneider, Erich , Ye, Qi-Zhuang, Bernhardt, Günther, Seifert, Roland und Buschauer, Armin (2006) Synthesis and pharmacological characterization of novel fluorescent histamine H2-receptor ligands derived from aminopotentidine. Bioorganic & Medicinal Chemistry Letters 16 (15), S. 3886-3890. Volltext nicht vorhanden.

Li, Liantao, Mayer, Matthias, Schneider, Erich , Schreiber, Elvira, Bernhardt, Günther, Peng, Shiqi und Buschauer, Armin (2003) Preparation of fluorescent nonpeptidic neuropeptide Y receptor ligands: analogues of the quinazoline-type anti-obesity Y5 antagonist CGP 71683A. Arch Pharm (Weinheim) 336 (12), S. 585-590. Volltext nicht vorhanden.