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The Journal of Biological Chemistry|November 25, 2010
Amino acid residues constituting the agonist binding site of the human P2X3 receptorMandy Bodnar, Haihong Wang, Thomas Riedel, et al.
The Journal of Biological Chemistry|March 2, 2012
ATP binding site mutagenesis reveals different subunit stoichiometry of functional P2X2/3 and P2X2/6 receptorsRalf Hausmann, Mandy Bodnar, Ronja Woltersdorf, et al.
British Journal of Pharmacology|July 15, 2020
Uncoupling sodium channel dimers restores the phenotype of a pain-linked Nav 1.7 channel mutationAnnika H Rühlmann, Jannis Körner, Ralf Hausmann, et al.
Nature Communications|August 19, 2018
Author Correction: The ASIC3/P2X3 cognate receptor is a pain-relevant and ligand-gated cationic channelGabriele Stephan, Lumei Huang, Yong Tang, et al.
Purinergic Signalling|May 29, 2021
BAC transgenic mice to study the expression of P2X2 and P2Y1 receptorsMarcus Grohmann, Michaela Schumacher, Janka Günther, et al.
British Journal of Pharmacology|October 30, 2020
Update of P2X receptor properties and their pharmacology: IUPHAR Review 30Peter Illes, Christa E Müller, Kenneth A Jacobson, et al.
Nature Communications|April 12, 2018
The ASIC3/P2X3 cognate receptor is a pain-relevant and ligand-gated cationic channelGabriele Stephan, Lumei Huang, Yong Tang, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|May 1, 2026
Functional Analysis of Ligand-Gated Chloride Channels in a Cnidarian Sheds Light on the Evolution of Inhibitory SignalingAbhilasha Ojha, Linda Kloss, Juan D Montenegro, et al.
International Journal of Molecular Sciences|April 13, 2018
β-Nicotinamide Adenine Dinucleotide (β-NAD) Inhibits ATP-Dependent IL-1β Release from Human Monocytic CellsSebastian Daniel Hiller, Sarah Heldmann, Katrin Richter, et al.
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