Papers associated with right (and p2rx4)

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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.
	Comparative Embryonic Spatio-Temporal Expression Profile Map of the Xenopus P2X Receptor Family., Blanchard C., Front Cell Neurosci. January 1, 2019; 13 340.
	Interaction of Purinergic P2X4 and P2X7 Receptor Subunits., Schneider M., Front Pharmacol. May 26, 2017; 8 860.
	Conserved extracellular cysteines differentially regulate the potentiation produced by Zn2+ in rat P2X4 receptors., Li CY., Eur J Pharmacol. May 5, 2013; 707 (1-3): 11-6.
	[Mg(2+) inhibits ATP-activated current mediated by rat P2X4 receptors expressed in Xenopus oocytes]., Peng F., Sheng Li Xue Bao. February 25, 2012; 64 (1): 75-81.
	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.
	The mechanism by which ethanol inhibits rat P2X4 receptors is altered by mutation of histidine 241., Xiong K., Br J Pharmacol. July 1, 2005; 145 (5): 576-86.
	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.
	Ethanol sensitivity in ATP-gated P2X receptors is subunit dependent., Davies DL., Alcohol Clin Exp Res. June 1, 2002; 26 (6): 773-8.
	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.
	Modulation of ATP-responses at recombinant rP2X4 receptors by extracellular pH and zinc., Wildman SS., Br J Pharmacol. February 1, 1999; 126 (3): 762-8.
	Antagonistic properties of the suramin analogue NF023 at heterologously expressed P2X receptors., Soto F., Neuropharmacology. January 1, 1999; 38 (1): 141-9.

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