Gunther Schmalzing

Affiliations: 
Goethe University, Frankfurt am Main 
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"Gunther Schmalzing"
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Hausmann R, Franke H, Schmalzing G. (2021) How Prof. Burnstock's enthusiasm supported P2 receptor research in Germany. Purinergic Signalling
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
Stephan G, Huang L, Tang Y, et al. (2018) The ASIC3/P2X3 cognate receptor is a pain-relevant and ligand-gated cationic channel. Nature Communications. 9: 1354
Xie J, Liu S, Wu B, et al. (2016) The protective effect of resveratrol in the transmission of neuropathic pain mediated by the P2X7 receptor in the dorsal root ganglia. Neurochemistry International
Stephan G, Kowalski-Jahn M, Zens C, et al. (2016) Inter-subunit disulfide locking of the human P2X3 receptor elucidates ectodomain movements associated with channel gating. Purinergic Signalling. 12: 221-33
Kowalski M, Hausmann R, Schmid J, et al. (2015) Flexible subunit stoichiometry of functional human P2X2/3 heteromeric receptors. Neuropharmacology
Hausmann R, Kless A, Schmalzing G. (2015) Key sites for P2X receptor function and multimerization: overview of mutagenesis studies on a structural basis. Current Medicinal Chemistry. 22: 799-818
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