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

Papers associated with p2rx4



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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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.            

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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

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.

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.

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.

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.

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