Interaction of Purinergic P2X4 and P2X7 Receptor Subunits.

Autor: Schneider M; Julius-Bernstein-Institute for Physiology, Martin-Luther-University, Halle, Germany., Prudic K; Julius-Bernstein-Institute for Physiology, Martin-Luther-University, Halle, Germany., Pippel A; Julius-Bernstein-Institute for Physiology, Martin-Luther-University, Halle, Germany., Klapperstück M; Julius-Bernstein-Institute for Physiology, Martin-Luther-University, Halle, Germany., Braam U; Molecular Pharmacology, RWTH Aachen University, Aachen, Germany., Müller CE; Pharmaceutical Institute, Pharmaceutical Chemistry I, University of Bonn, Bonn, Germany., Schmalzing G; Molecular Pharmacology, RWTH Aachen University, Aachen, Germany., Markwardt F; Julius-Bernstein-Institute for Physiology, Martin-Luther-University, Halle, Germany.

Publikováno v: Frontiers in pharmacology [Front Pharmacol] 2017 Nov 22; Vol. 8, pp. 860. Date of Electronic Publication: 2017 Nov 22 (Print Publication: 2017).

P2X7 Receptor-Induced Human Mast Cell Degranulation Is Enhanced by Interleukin 33.

Autor: Salcman, Barbora¹ (AUTHOR) barbora.salcman@manchester.ac.uk, Bahri, Rajia¹ (AUTHOR) rajia.bahri-2@manchester.ac.uk, West, Peter W.¹ (AUTHOR) peter.west@manchester.ac.uk, Tontini, Chiara¹ (AUTHOR) chiara.tontini@postgrad.manchester.ac.uk, Affleck, Karen² (AUTHOR) karen.x.affleck@gsk.com, Bulfone-Paus, Silvia¹ (AUTHOR) silvia.bulfone-paus@manchester.ac.uk

Publikováno v: International Journal of Molecular Sciences. Feb2024, Vol. 25 Issue 3, p1730. 17p.

A hydrophobic residue in position 15 of the rP2X3 receptor slows desensitization and reveals properties beneficial for pharmacological analysis and high-throughput screening.

Autor: Hausmann R; Department of Molecular Pharmacology, Medical Faculty of the RWTH Aachen University, Wendlingweg 2, 52074 Aachen, Germany. Electronic address: rhausmann@ukaachen.de., Bahrenberg G; Grünenthal GmbH, Global Drug Discovery, Department of Molecular Pharmacology, Zieglerstrasse 6, 52078 Aachen, Germany., Kuhlmann D; Department of Molecular Pharmacology, Medical Faculty of the RWTH Aachen University, Wendlingweg 2, 52074 Aachen, Germany., Schumacher M; Department of Molecular Pharmacology, Medical Faculty of the RWTH Aachen University, Wendlingweg 2, 52074 Aachen, Germany., Braam U; Department of Molecular Pharmacology, Medical Faculty of the RWTH Aachen University, Wendlingweg 2, 52074 Aachen, Germany., Bieler D; Grünenthal GmbH, Global Drug Discovery, Department of Molecular Pharmacology, Zieglerstrasse 6, 52078 Aachen, Germany., Schlusche I; Grünenthal GmbH, Global Drug Discovery, Department of Molecular Pharmacology, Zieglerstrasse 6, 52078 Aachen, Germany., Schmalzing G; Department of Molecular Pharmacology, Medical Faculty of the RWTH Aachen University, Wendlingweg 2, 52074 Aachen, Germany.

Publikováno v: Neuropharmacology [Neuropharmacology] 2014 Apr; Vol. 79, pp. 603-15. Date of Electronic Publication: 2014 Jan 19.

Effects of calmodulin antagonists on human adenoidal mast cells.

Autor: Bent, S., Braam, U., Schmutzler, W.

Publikováno v: Agents & Actions; Apr1990, Vol. 30 Issue 1/2, p121-124, 4p

TMEM16A(a)/anoctamin-1 shares a homodimeric architecture with CLC chloride channels.

Autor: Fallah G; Molecular Pharmacology, RWTH Aachen University, Aachen, Germany., Römer T, Detro-Dassen S, Braam U, Markwardt F, Schmalzing G

Publikováno v: Molecular & cellular proteomics : MCP [Mol Cell Proteomics] 2011 Feb; Vol. 10 (2), pp. M110.004697. Date of Electronic Publication: 2010 Oct 25.