Gunther Schmalzing
Affiliations: | Goethe University, Frankfurt am Main |
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Sign in to add traineeArmaz Aschrafi | grad student | 1998-2002 | Goethe University, Frankfurt am Main |
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Grohs L, Cheng L, Cönen S, et al. (2023) Diclofenac and other non-steroidal anti-inflammatory drugs (NSAIDs) are competitive antagonists of the human P2X3 receptor. Frontiers in Pharmacology. 14: 1120360 |
Schmalzing G, Markwardt F. (2022) Established Protocols for cRNA Expression and Voltage-Clamp Characterization of the P2X7 Receptor in Xenopus laevis Oocytes. Methods in Molecular Biology (Clifton, N.J.). 2510: 157-192 |
Schiller IC, Jacobson KA, Wen Z, et al. (2022) Dihydropyridines Potentiate ATP-Induced Currents Mediated by the Full-Length Human P2X5 Receptor. Molecules (Basel, Switzerland). 27 |
Trang M, Schmalzing G, Müller CE, et al. (2020) Dissection of P2X4 and P2X7 Receptor Current Components in BV-2 Microglia. International Journal of Molecular Sciences. 21 |
Illes P, Müller CE, Jacobson KA, et al. (2020) Update of P2X receptor properties and their pharmacology: IUPHAR Review 30. British Journal of Pharmacology |
Rühlmann AH, Körner J, Hausmann R, et al. (2020) Uncoupling sodium channel dimers rescues the phenotype of a pain-linked Nav1.7 mutation. British Journal of Pharmacology |
Obrecht AS, Urban N, Schaefer M, et al. (2019) Identification of aurintricarboxylic acid as a potent allosteric antagonist of P2X1 and P2X3 receptors. Neuropharmacology. 107749 |
Stephan G, Huang L, Tang Y, et al. (2018) Author Correction: The ASIC3/P2X3 cognate receptor is a pain-relevant and ligand-gated cationic channel. Nature Communications. 9: 3351 |
Kaluza L, Meents JE, Hampl M, et al. (2018) Loss-of-function of Nav1.8/D1639N linked to human pain can be rescued by lidocaine. Pflugers Archiv : European Journal of Physiology |
Hiller SD, Heldmann S, Richter K, et al. (2018) β-Nicotinamide Adenine Dinucleotide (β-NAD) Inhibits ATP-Dependent IL-1β Release from Human Monocytic Cells. International Journal of Molecular Sciences. 19 |