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Residues in Transmembrane Segments of the P2X4 Receptor Contribute to Channel Function and Ethanol Sensitivity. , Popova M., Int J Mol Sci. April 2, 2020; 21 (7):
Bile acids inhibit human purinergic receptor P2X4 in a heterologous expression system. , Ilyaskin AV., J Gen Physiol. June 3, 2019; 151 (6): 820-833.
Mapping the binding site of the P2X receptor antagonist PPADS reveals the importance of orthosteric site charge and the cysteine-rich head region. , Huo H., J Biol Chem. August 17, 2018; 293 (33): 12820-12831.
Interaction of Purinergic P2X4 and P2X7 Receptor Subunits. , Schneider M., Front Pharmacol. May 26, 2017; 8 860.
High Ca(2+) permeability of a peptide-gated DEG/ENaC from Hydra. , Dürrnagel S., J Gen Physiol. October 1, 2012; 140 (4): 391-402.
[Characteristic and effect of cadmium on ATP-activated currents mediated by P2X4 receptors]. , Zhang YQ , Zhang YQ ., Zhongguo Ying Yong Sheng Li Xue Za Zhi. September 1, 2012; 28 (5): 430-4.
Covalent modification of mutant rat P2X2 receptors with a thiol-reactive fluorophore allows channel activation by zinc or acidic pH without ATP. , Dellal SS., PLoS One. January 1, 2012; 7 (10): e47147.
Cysteine scanning mutagenesis (residues Glu52-Gly96) of the human P2X1 receptor for ATP: mapping agonist binding and channel gating. , Allsopp RC., J Biol Chem. August 19, 2011; 286 (33): 29207-17.
Purinergic receptor-mediated Ca signaling in the olfactory bulb and the neurogenic area of the lateral ventricles. , Hassenklöver T ., Purinergic Signal. December 1, 2010; 6 (4): 429-45.
Secondary structure and gating rearrangements of transmembrane segments in rat P2X4 receptor channels. , Silberberg SD., J Gen Physiol. April 1, 2005; 125 (4): 347-59.
Molecular cloning and functional expression of Xenopus laevis oocyte ATP-activated P2X4 channels. , Juranka PF., Biochim Biophys Acta. May 2, 2001; 1512 (1): 111-24.
Differential modulation by copper and zinc of P2X2 and P2X4 receptor function. , Xiong K., J Neurophysiol. May 1, 1999; 81 (5): 2088-94.