Papers associated with p2rx4

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	Agonist binding evokes extensive conformational changes in the extracellular domain of the ATP-gated human P2X1 receptor ion channel., Roberts JA, Allsopp RC, El Ajouz S, Vial C, Schmid R, Young MT, Evans RJ., Proc Natl Acad Sci U S A. March 20, 2012; 109 (12): 4663-7.
	P2X2 and P2X5 subunits define a new heteromeric receptor with P2X7-like properties., Compan V, Ulmann L, Stelmashenko O, Chemin J, Chaumont S, Rassendren F., J Neurosci. March 21, 2012; 32 (12): 4284-96.
	P2X4 receptor channels form large noncytolytic pores in resting and activated microglia., Bernier LP, Ase AR, Boué-Grabot E, Séguéla P., Glia. May 1, 2012; 60 (5): 728-37.
	Involvement of the cysteine-rich head domain in activation and desensitization of the P2X1 receptor., Lörinczi É, Bhargava Y, Marino SF, Taly A, Kaczmarek-Hájek K, Barrantes-Freer A, Dutertre S, Grutter T, Rettinger J, Nicke A., Proc Natl Acad Sci U S A. July 10, 2012; 109 (28): 11396-401.
	Ivermectin reduces alcohol intake and preference in mice., Yardley MM, Wyatt L, Khoja S, Asatryan L, Ramaker MJ, Finn DA, Alkana RL, Huynh N, Louie SG, Petasis NA, Bortolato M, Davies DL., Neuropharmacology. August 1, 2012; 63 (2): 190-201.
	[Characteristic and effect of cadmium on ATP-activated currents mediated by P2X4 receptors]., Zhang YQ, Zhang YQ, Tian WH, Peng F, Xu Z, Nie YL., Zhongguo Ying Yong Sheng Li Xue Za Zhi. September 1, 2012; 28 (5): 430-4.
	High Ca(2+) permeability of a peptide-gated DEG/ENaC from Hydra., Dürrnagel S, Falkenburger BH, Gründer S., J Gen Physiol. October 1, 2012; 140 (4): 391-402.
	Salt bridge switching from Arg290/Glu167 to Arg290/ATP promotes the closed-to-open transition of the P2X2 receptor., Hausmann R, Günther J, Kless A, Kuhlmann D, Kassack MU, Bahrenberg G, Markwardt F, Schmalzing G., Mol Pharmacol. January 1, 2013; 83 (1): 73-84.
	Conserved extracellular cysteines differentially regulate the potentiation produced by Zn2+ in rat P2X4 receptors., Li CY, Xiong KM, Wu YX, Liu YW, Chen L, Stewart RR, Peoples RW, Yi CL., Eur J Pharmacol. May 5, 2013; 707 (1-3): 11-6.
	Tryptophan 46 is a site for ethanol and ivermectin action in P2X4 receptors., Popova M, Trudell J, Li K, Alkana R, Davies D, Asatryan L., Purinergic Signal. December 1, 2013; 9 (4): 621-32.
	Avermectins differentially affect ethanol intake and receptor function: implications for developing new therapeutics for alcohol use disorders., Asatryan L, Yardley MM, Khoja S, Trudell JR, Hyunh N, Louie SG, Petasis NA, Alkana RL, Davies DL., Int J Neuropsychopharmacol. June 1, 2014; 17 (6): 907-16.
	Signal transmission within the P2X2 trimeric receptor., Keceli B, Kubo Y., J Gen Physiol. June 1, 2014; 143 (6): 761-82.
	Basolateral P2X₄channels stimulate ENaC activity in Xenopus cortical collecting duct A6 cells., Thai TL, Yu L, Eaton DC, Duke BJ, Al-Khalili O, Lam HY, Ma H, Bao HF., Am J Physiol Renal Physiol. October 1, 2014; 307 (7): F806-13.
	Use of chimeras, point mutants, and molecular modeling to map the antagonist-binding site of 4,4',4″,4‴-(carbonylbis-(imino-5,1,3-benzenetriylbis(carbonylimino)))tetrakisbenzene-1,3-disulfonic acid (NF449) at P2X1 receptors for ATP., Farmer LK, Schmid R, Evans RJ., J Biol Chem. January 16, 2015; 290 (3): 1559-69.
	Lidocaine preferentially inhibits the function of purinergic P2X7 receptors expressed in Xenopus oocytes., Okura D, Horishita T, Ueno S, Yanagihara N, Sudo Y, Uezono Y, Minami T, Kawasaki T, Sata T., Anesth Analg. March 1, 2015; 120 (3): 597-605.
	Two P2X1 receptor transcripts able to form functional channels are present in most human monocytes., López-López C, Jaramillo-Polanco J, Portales-Pérez DP, Gómez-Coronado KS, Rodríguez-Meléndez JG, Cortés-García JD, Espinosa-Luna R, Montaño LM, Barajas-López C., Eur J Pharmacol. December 15, 2016; 793 82-88.
	Preclinical development of moxidectin as a novel therapeutic for alcohol use disorder., Huynh N, Arabian N, Naito A, Louie S, Jakowec MW, Asatryan L, Davies DL., Neuropharmacology. February 1, 2017; 113 (Pt A): 60-70.
	Structural insights into the nucleotide base specificity of P2X receptors., Kasuya G, Fujiwara Y, Tsukamoto H, Morinaga S, Ryu S, Touhara K, Ishitani R, Furutani Y, Hattori M, Nureki O., Sci Rep. March 23, 2017; 7 45208.
	Interaction of Purinergic P2X4 and P2X7 Receptor Subunits., Schneider M, Prudic K, Pippel A, Klapperstück M, Braam U, Müller CE, Schmalzing G, Markwardt F., Front Pharmacol. May 26, 2017; 8 860.
	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, Fryatt AG, Farmer LK, Schmid R, Evans RJ., J Biol Chem. August 17, 2018; 293 (33): 12820-12831.
	Comparative Embryonic Spatio-Temporal Expression Profile Map of the Xenopus P2X Receptor Family., Blanchard C, Boué-Grabot E, Massé K., Front Cell Neurosci. January 1, 2019; 13 340.
	Bile acids inhibit human purinergic receptor P2X4 in a heterologous expression system., Ilyaskin AV, Sure F, Nesterov V, Haerteis S, Korbmacher C., J Gen Physiol. June 3, 2019; 151 (6): 820-833.
	A challenge finding P2X1 and P2X4 ligands., Beswick P, Wahab B, Honey MA, Paradowski M, Jiang K, Lochner M, Murrell-Lagnado RD, Thompson AJ., Neuropharmacology. October 1, 2019; 157 107674.
	Identification of aurintricarboxylic acid as a potent allosteric antagonist of P2X1 and P2X3 receptors., Obrecht AS, Urban N, Schaefer M, Röse A, Kless A, Meents JE, Lampert A, Abdelrahman A, Müller CE, Schmalzing G, Hausmann R., Neuropharmacology. November 1, 2019; 158 107749.
	Residues in Transmembrane Segments of the P2X4 Receptor Contribute to Channel Function and Ethanol Sensitivity., Popova M, Rodriguez L, Trudell JR, Nguyen S, Bloomfield M, Davies DL, Asatryan L., Int J Mol Sci. April 2, 2020; 21 (7):
	Cross-Talk between P2X and NMDA Receptors., Rodriguez L, Yi C, Chu C, Duriez Q, Watanabe S, Ryu M, Reyes B, Asatryan L, Boué-Grabot E, Davies D., Int J Mol Sci. September 29, 2020; 21 (19):
	Dissection of P2X4 and P2X7 Receptor Current Components in BV-2 Microglia., Trang M, Schmalzing G, Müller CE, Markwardt F., Int J Mol Sci. November 11, 2020; 21 (22):

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