Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (77) GO Terms (6) Nucleotides (123) Proteins (58) Interactants (71) Wiki
XB-GENEPAGE-967964

Papers associated with p2rx4



???displayGene.coCitedPapers???

???pagination.result.count???

???pagination.result.page??? 1 2 ???pagination.result.next???

Sort Newest To Oldest Sort Oldest To Newest

P2X4: an ATP-activated ionotropic receptor cloned from rat brain., Soto F, Garcia-Guzman M, Gomez-Hernandez JM, Hollmann M, Karschin C, Stühmer W., Proc Natl Acad Sci U S A. April 16, 1996; 93 (8): 3684-8.


Cloning and tissue distribution of a novel P2X receptor from rat brain., Soto F, Garcia-Guzman M, Karschin C, Stühmer W., Biochem Biophys Res Commun. June 14, 1996; 223 (2): 456-60.


Neuropharmacology: a part for purines in pattern generation., Halliday FC, Gibb AJ., Curr Biol. January 1, 1997; 7 (1): R47-9.


Characterization of recombinant human P2X4 receptor reveals pharmacological differences to the rat homologue., Garcia-Guzman M, Soto F, Gomez-Hernandez JM, Lund PE, Stühmer W., Mol Pharmacol. January 1, 1997; 51 (1): 109-18.


Effects of neuroamines and divalent cations on cloned and mutated ATP-gated channels., Nakazawa K, Ohno Y., Eur J Pharmacol. April 23, 1997; 325 (1): 101-8.


The human P2X4 receptor gene is alternatively spliced., Dhulipala PD, Wang YX, Kotlikoff MI., Gene. January 30, 1998; 207 (2): 259-66.


A pyridoxine cyclic phosphate and its 6-azoaryl derivative selectively potentiate and antagonize activation of P2X1 receptors., Jacobson KA, Kim YC, Wildman SS, Mohanram A, Harden TK, Boyer JL, King BF, Burnstock G., J Med Chem. June 18, 1998; 41 (13): 2201-6.


Central P2X4 and P2X6 channel subunits coassemble into a novel heteromeric ATP receptor., Lê KT, Babinski K, Séguéla P., J Neurosci. September 15, 1998; 18 (18): 7152-9.


Antagonistic properties of the suramin analogue NF023 at heterologously expressed P2X receptors., Soto F, Lambrecht G, Nickel P, Stühmer W, Busch AE., Neuropharmacology. January 1, 1999; 38 (1): 141-9.


Modulation of ATP-responses at recombinant rP2X4 receptors by extracellular pH and zinc., Wildman SS, King BF, Burnstock G., Br J Pharmacol. February 1, 1999; 126 (3): 762-8.


Molecular cloning, functional characterization and possible cooperativity between the murine P2X4 and P2X4a receptors., Townsend-Nicholson A, King BF, Wildman SS, Burnstock G., Brain Res Mol Brain Res. February 5, 1999; 64 (2): 246-54.


Selectivity of diadenosine polyphosphates for rat P2X receptor subunits., Wildman SS, Brown SG, King BF, Burnstock G., Eur J Pharmacol. February 12, 1999; 367 (1): 119-23.


Differential modulation by copper and zinc of P2X2 and P2X4 receptor function., Xiong K, Peoples RW, Montgomery JP, Chiang Y, Stewart RR, Weight FF, Li C., J Neurophysiol. May 1, 1999; 81 (5): 2088-94.


Site-specific splice variation of the human P2X4 receptor., Carpenter D, Meadows HJ, Brough S, Chapman G, Clarke C, Coldwell M, Davis R, Harrison D, Meakin J, McHale M, Rice SQ, Tomlinson WJ, Wood M, Sanger GJ., Neurosci Lett. October 8, 1999; 273 (3): 183-6.


Mutation of histidine 286 of the human P2X4 purinoceptor removes extracellular pH sensitivity., Clarke CE, Benham CD, Bridges A, George AR, Meadows HJ., J Physiol. March 15, 2000; 523 Pt 3 697-703.


Zinc and copper modulate differentially the P2X4 receptor., Acuña-Castillo C, Morales B, Huidobro-Toro JP., J Neurochem. April 1, 2000; 74 (4): 1529-37.


Molecular cloning and functional expression of Xenopus laevis oocyte ATP-activated P2X4 channels., Juranka PF, Haghighi AP, Gaertner T, Cooper E, Morris CE., Biochim Biophys Acta. May 2, 2001; 1512 (1): 111-24.            


Formation of carnosine-Cu(II) complexes prevents and reverts the inhibitory action of copper in P2X4 and P2X7 receptors., Coddou C, Villalobos C, González J, Acuña-Castillo C, Loeb B, Huidobro-Toro JP., J Neurochem. February 1, 2002; 80 (4): 626-33.


Ethanol sensitivity in ATP-gated P2X receptors is subunit dependent., Davies DL, Machu TK, Guo Y, Alkana RL., Alcohol Clin Exp Res. June 1, 2002; 26 (6): 773-8.


The human prion octarepeat fragment prevents and reverses the inhibitory action of copper in the P2X4 receptor without modifying the zinc action., Lorca RA, Chacón M, Barría MI, Inestrosa NC, Huidobro-Toro JP., J Neurochem. May 1, 2003; 85 (3): 709-16.


Neuromodulator role of zinc and copper during prolonged ATP applications to P2X4 purinoceptors., Coddou C, Morales B, Huidobro-Toro JP., Eur J Pharmacol. July 4, 2003; 472 (1-2): 49-56.


Histidine 140 plays a key role in the inhibitory modulation of the P2X4 nucleotide receptor by copper but not zinc., Coddou C, Morales B, González J, Grauso M, Gordillo F, Bull P, Rassendren F, Huidobro-Toro JP., J Biol Chem. September 19, 2003; 278 (38): 36777-85.


Role of extracellular histidines in agonist sensitivity of the rat P2X4 receptor., Xiong K, Stewart RR, Hu XQ, Werby E, Peoples RW, Weight FF, Li C., Neurosci Lett. July 29, 2004; 365 (3): 195-9.


Role of extracellular histidines in antagonist sensitivity of the rat P2X4 receptor., Xiong K, Stewart RR, Weight FF, Li C., Neurosci Lett. September 2, 2004; 367 (2): 197-200.


Trimeric architecture of homomeric P2X2 and heteromeric P2X1+2 receptor subtypes., Aschrafi A, Sadtler S, Niculescu C, Rettinger J, Schmalzing G., J Mol Biol. September 3, 2004; 342 (1): 333-43.


Heavy metals modulate the activity of the purinergic P2X4 receptor., Coddou C, Lorca RA, Acuña-Castillo C, Grauso M, Rassendren F, Huidobro-Toro JP., Toxicol Appl Pharmacol. January 15, 2005; 202 (2): 121-31.


Biochemical and functional evidence for heteromeric assembly of P2X1 and P2X4 subunits., Nicke A, Kerschensteiner D, Soto F., J Neurochem. February 1, 2005; 92 (4): 925-33.


Secondary structure and gating rearrangements of transmembrane segments in rat P2X4 receptor channels., Silberberg SD, Chang TH, Swartz KJ., J Gen Physiol. April 1, 2005; 125 (4): 347-59.                


The mechanism by which ethanol inhibits rat P2X4 receptors is altered by mutation of histidine 241., Xiong K, Hu XQ, Stewart RR, Weight FF, Li C., Br J Pharmacol. July 1, 2005; 145 (5): 576-86.


Regulatory interdependence of cloned epithelial Na+ channels and P2X receptors., Wildman SS, Marks J, Churchill LJ, Peppiatt CM, Chraibi A, Shirley DG, Horisberger JD, King BF, Unwin RJ., J Am Soc Nephrol. September 1, 2005; 16 (9): 2586-97.


Differential effects of propofol and ethanol on P2X4 receptors expressed in Xenopus oocytes., Davies DL, Kuo ST, Alkana RL., Int Congr Ser. November 1, 2005; 1283 285-287.


Basolateral P2X4-like receptors regulate the extracellular ATP-stimulated epithelial Na+ channel activity in renal epithelia., Zhang Y, Sanchez D, Gorelik J, Klenerman D, Lab M, Edwards C, Korchev Y., Am J Physiol Renal Physiol. June 1, 2007; 292 (6): F1734-40.


Dissecting the facilitator and inhibitor allosteric metal sites of the P2X4 receptor channel: critical roles of CYS132 for zinc potentiation and ASP138 for copper inhibition., Coddou C, Acuña-Castillo C, Bull P, Huidobro-Toro JP., J Biol Chem. December 21, 2007; 282 (51): 36879-86.


Cysteine substitution mutagenesis and the effects of methanethiosulfonate reagents at P2X2 and P2X4 receptors support a core common mode of ATP action at P2X receptors., Roberts JA, Digby HR, Kara M, El Ajouz S, Sutcliffe MJ, Evans RJ., J Biol Chem. July 18, 2008; 283 (29): 20126-36.                


Phosphoinositides regulate P2X4 ATP-gated channels through direct interactions., Bernier LP, Ase AR, Chevallier S, Blais D, Zhao Q, Boué-Grabot E, Logothetis D, Séguéla P., J Neurosci. November 26, 2008; 28 (48): 12938-45.


Homotrimeric complexes are the dominant assembly state of native P2X7 subunits., Nicke A., Biochem Biophys Res Commun. December 19, 2008; 377 (3): 803-8.


Conserved extracellular cysteines differentially regulate the inhibitory effect of ethanol in rat P2X4 receptors., Yi CL, Liu YW, Xiong KM, Stewart RR, Peoples RW, Tian X, Zhou L, Ai YX, Li ZW, Wang QW, Li CY., Biochem Biophys Res Commun. March 27, 2009; 381 (1): 102-6.


Neurosteroids differentially modulate P2X ATP-gated channels through non-genomic interactions., Codocedo JF, Rodríguez FE, Huidobro-Toro JP., J Neurochem. July 1, 2009; 110 (2): 734-44.


Reactive oxygen species potentiate the P2X2 receptor activity through intracellular Cys430., Coddou C, Codocedo JF, Li S, Lillo JG, Acuña-Castillo C, Bull P, Stojilkovic SS, Huidobro-Toro JP., J Neurosci. September 30, 2009; 29 (39): 12284-91.


A point mutation in the ectodomain-transmembrane 2 interface eliminates the inhibitory effects of ethanol in P2X4 receptors., Popova M, Asatryan L, Ostrovskaya O, Wyatt LR, Li K, Alkana RL, Davies DL., J Neurochem. January 1, 2010; 112 (1): 307-17.


Selective potentiation of homomeric P2X2 ionotropic ATP receptors by a fast non-genomic action of progesterone., De Roo M, Boué-Grabot E, Schlichter R., Neuropharmacology. March 1, 2010; 58 (3): 569-77.


Ivermectin antagonizes ethanol inhibition in purinergic P2X4 receptors., Asatryan L, Popova M, Perkins D, Trudell JR, Alkana RL, Davies DL., J Pharmacol Exp Ther. September 1, 2010; 334 (3): 720-8.


Purinergic receptor-mediated Ca signaling in the olfactory bulb and the neurogenic area of the lateral ventricles., Hassenklöver T, Schulz P, Peters A, Schwartz P, Schild D, Manzini I., Purinergic Signal. December 1, 2010; 6 (4): 429-45.                


Discovery of potent competitive antagonists and positive modulators of the P2X2 receptor., Baqi Y, Hausmann R, Rosefort C, Rettinger J, Schmalzing G, Müller CE., J Med Chem. February 10, 2011; 54 (3): 817-30.


Cross-talk between P2X4 and gamma-aminobutyric acid, type A receptors determines synaptic efficacy at a central synapse., Jo YH, Donier E, Martinez A, Garret M, Toulmé E, Boué-Grabot E., J Biol Chem. June 3, 2011; 286 (22): 19993-20004.


Cysteine scanning mutagenesis (residues Glu52-Gly96) of the human P2X1 receptor for ATP: mapping agonist binding and channel gating., Allsopp RC, El Ajouz S, Schmid R, Evans RJ., J Biol Chem. August 19, 2011; 286 (33): 29207-17.              


Molecular basis of selective antagonism of the P2X1 receptor for ATP by NF449 and suramin: contribution of basic amino acids in the cysteine-rich loop., El-Ajouz S, Ray D, Allsopp RC, Evans RJ., Br J Pharmacol. January 1, 2012; 165 (2): 390-400.          


Covalent modification of mutant rat P2X2 receptors with a thiol-reactive fluorophore allows channel activation by zinc or acidic pH without ATP., Dellal SS, Hume RI., PLoS One. January 1, 2012; 7 (10): e47147.                    


Cloning and characterization of a P2X receptor expressed in the central nervous system of Lymnaea stagnalis., Bavan S, Straub VA, Webb TE, Ennion SJ., PLoS One. January 1, 2012; 7 (11): e50487.                


[Mg(2+) inhibits ATP-activated current mediated by rat P2X4 receptors expressed in Xenopus oocytes]., Peng F, Zhang YQ, Zhang YQ, Zeng Y, Zhou YL., Sheng Li Xue Bao. February 25, 2012; 64 (1): 75-81.

???pagination.result.page??? 1 2 ???pagination.result.next???