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Summary Expression Phenotypes Gene Literature (308) GO Terms (6) Nucleotides (92) Proteins (53) Interactants (177) Wiki
XB-GENEPAGE-1004370

Papers associated with kcnj3



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Evidence for sequential ion-binding loci along the inner pore of the IRK1 inward-rectifier K+ channel., Shin HG, Xu Y, Xu Y, Lu Z., J Gen Physiol. August 1, 2005; 126 (2): 123-35.                            

Tertiapin-Q blocks recombinant and native large conductance K+ channels in a use-dependent manner., Kanjhan R, Coulson EJ, Adams DJ, Bellingham MC., J Pharmacol Exp Ther. September 1, 2005; 314 (3): 1353-61.

A difference in inward rectification and polyamine block and permeation between the Kir2.1 and Kir3.1/Kir3.4 K+ channels., Makary SM, Claydon TW, Enkvetchakul D, Nichols CG, Boyett MR., J Physiol. November 1, 2005; 568 (Pt 3): 749-66.

Differential ion current activation by human 5-HT(1A) receptors in Xenopus oocytes: evidence for agonist-directed trafficking of receptor signalling., Heusler P, Pauwels PJ, Wurch T, Newman-Tancredi A, Tytgat J, Colpaert FC, Cussac D., Neuropharmacology. December 1, 2005; 49 (7): 963-76.

Tyrosine phosphorylation of K(ir)3.1 in spinal cord is induced by acute inflammation, chronic neuropathic pain, and behavioral stress., Ippolito DL, Xu M, Bruchas MR, Wickman K, Chavkin C., J Biol Chem. December 16, 2005; 280 (50): 41683-93.

G protein-activated inwardly rectifying K+ channel inhibition and rescue of weaver mouse motor functions by antidepressants., Takahashi T, Kobayashi T, Ozaki M, Takamatsu Y, Ogai Y, Ohta M, Yamamoto H, Ikeda K., Neurosci Res. February 1, 2006; 54 (2): 104-11.

Inhibition of G protein-activated inwardly rectifying K+ channels by ifenprodil., Kobayashi T, Washiyama K, Ikeda K., Neuropsychopharmacology. March 1, 2006; 31 (3): 516-24.

Hydrogen-bonding dynamics between adjacent blades in G-protein beta-subunit regulates GIRK channel activation., Mirshahi T, Logothetis DE, Rosenhouse-Dantsker A., Biophys J. April 15, 2006; 90 (8): 2776-85.

Effects of the abused inhalant toluene on ethanol-sensitive potassium channels expressed in oocytes., Del Re AM, Dopico AM, Woodward JJ., Dev Biol. May 4, 2006; 1087 (1): 75-82.

Modulation of basal and receptor-induced GIRK potassium channel activity and neuronal excitability by the mammalian PINS homolog LGN., Wiser O, Qian X, Ehlers M, Ja WW, Roberts RW, Reuveny E, Jan YN, Jan LY., Neuron. May 18, 2006; 50 (4): 561-73.

Base of pore loop is important for rectification, activation, permeation, and block of Kir3.1/Kir3.4., Makary SM, Claydon TW, Dibb KM, Boyett MR., Biophys J. June 1, 2006; 90 (11): 4018-34.

Heterotrimeric G proteins form stable complexes with adenylyl cyclase and Kir3.1 channels in living cells., Rebois RV, Robitaille M, Galés C, Dupré DJ, Baragli A, Trieu P, Ethier N, Bouvier M, Hébert TE., J Cell Sci. July 1, 2006; 119 (Pt 13): 2807-18.

Inhibition of G protein-activated inwardly rectifying K+ channels by the antidepressant paroxetine., Kobayashi T, Washiyama K, Ikeda K., J Pharmacol Sci. November 1, 2006; 102 (3): 278-87.

RGS3 and RGS4 differentially associate with G protein-coupled receptor-Kir3 channel signaling complexes revealing two modes of RGS modulation. Precoupling and collision coupling., Jaén C, Doupnik CA., J Biol Chem. November 10, 2006; 281 (45): 34549-60.

Testosterone and progesterone rapidly attenuate plasma membrane Gbetagamma-mediated signaling in Xenopus laevis oocytes by signaling through classical steroid receptors., Evaul K, Jamnongjit M, Bhagavath B, Hammes SR., Mol Endocrinol. January 1, 2007; 21 (1): 186-96.

Inhibitory effect of gabapentin on N-methyl-D-aspartate receptors expressed in Xenopus oocytes., Hara K, Sata T., Acta Anaesthesiol Scand. January 1, 2007; 51 (1): 122-8.

The GIRK1 brain variant GIRK1d and its functional impact on heteromultimeric GIRK channels., Steinecker B, Rosker C, Schreibmayer W., J Recept Signal Transduct Res. January 1, 2007; 27 (5-6): 369-82.

Differential agonist and inverse agonist profile of antipsychotics at D2L receptors coupled to GIRK potassium channels., Heusler P, Newman-Tancredi A, Castro-Fernandez A, Cussac D., Neuropharmacology. March 1, 2007; 52 (4): 1106-13.

Galphai3 primes the G protein-activated K+ channels for activation by coexpressed Gbetagamma in intact Xenopus oocytes., Rubinstein M, Peleg S, Berlin S, Brass D, Dascal N., J Physiol. May 15, 2007; 581 (Pt 1): 17-32.

Functional activation by central monoamines of human dopamine D(4) receptor polymorphic variants coupled to GIRK channels in Xenopus oocytes., Wedemeyer C, Goutman JD, Avale ME, Franchini LF, Rubinstein M, Calvo DJ., Eur J Pharmacol. May 21, 2007; 562 (3): 165-73.

Inhibition by cocaine of G protein-activated inwardly rectifying K+ channels expressed in Xenopus oocytes., Kobayashi T, Nishizawa D, Iwamura T, Ikeda K., Toxicol In Vitro. June 1, 2007; 21 (4): 656-64.

The human histamine H3 receptor couples to GIRK channels in Xenopus oocytes., Sahlholm K, Nilsson J, Marcellino D, Fuxe K, Arhem P., Eur J Pharmacol. July 19, 2007; 567 (3): 206-10.

Characterizations of a loss-of-function mutation in the Kir3.4 channel subunit., Calloe K, Ravn LS, Schmitt N, Sui JL, Duno M, Haunso S, Grunnet M, Svendsen JH, Olesen SP., Biochem Biophys Res Commun. December 28, 2007; 364 (4): 889-95.

Identification of peptides that inhibit regulator of G protein signaling 4 function., Wang Y, Lee Y, Zhang J, Young KH., Pharmacology. January 1, 2008; 82 (2): 97-104.

Subunit stoichiometry of heterologously expressed G-protein activated inwardly rectifying potassium channels analysed by fluorescence intensity ratio measurement., Grasser E, Steinecker B, Ahammer H, Schreibmayer W., Pflugers Arch. March 1, 2008; 455 (6): 1017-24.

Agonist and antagonist properties of antipsychotics at human dopamine D4.4 receptors: G-protein activation and K+ channel modulation in transfected cells., Newman-Tancredi A, Heusler P, Martel JC, Ormière AM, Leduc N, Cussac D., Int J Neuropsychopharmacol. May 1, 2008; 11 (3): 293-307.

Voltage-dependence of the human dopamine D2 receptor., Sahlholm K, Nilsson J, Marcellino D, Fuxe K, Arhem P., Synapse. June 1, 2008; 62 (6): 476-80.

Electrophysiology-based analysis of human histamine H(4) receptor pharmacology using GIRK channel coupling in Xenopus oocytes., Sahlholm K, Nilsson J, Marcellino D, Fuxe K, Arhem P., Eur J Pharmacol. September 4, 2008; 591 (1-3): 52-8.

Increases in intracellular calcium triggered by channelrhodopsin-2 potentiate the response of metabotropic glutamate receptor mGluR7., Caldwell JH, Herin GA, Nagel G, Bamberg E, Scheschonka A, Betz H., J Biol Chem. September 5, 2008; 283 (36): 24300-7.

Differential voltage-sensitivity of D2-like dopamine receptors., Sahlholm K, Marcellino D, Nilsson J, Fuxe K, Rhem P., Biochem Biophys Res Commun. September 26, 2008; 374 (3): 496-501.

Activation gating kinetics of GIRK channels are mediated by cytoplasmic residues adjacent to transmembrane domains., Sadja R, Reuveny E., Channels (Austin). January 1, 2009; 3 (3): 205-14.

Inhibitory effects of the antiepileptic drug ethosuximide on G protein-activated inwardly rectifying K+ channels., Kobayashi T, Hirai H, Iino M, Fuse I, Mitsumura K, Washiyama K, Kasai S, Ikeda K., Neuropharmacology. February 1, 2009; 56 (2): 499-506.

Amplitude histogram-based method of analysis of patch clamp recordings that involve extreme changes in channel activity levels., Yakubovich D, Rishal I, Dessauer CW, Dascal N., J Mol Neurosci. March 1, 2009; 37 (3): 201-11.

Heteromeric assembly of inward rectifier channel subunit Kir2.1 with Kir3.1 and with Kir3.4., Ishihara K, Yamamoto T, Kubo Y., Biochem Biophys Res Commun. March 20, 2009; 380 (4): 832-7.

Divergent regulation of GIRK1 and GIRK2 subunits of the neuronal G protein gated K+ channel by GalphaiGDP and Gbetagamma., Rubinstein M, Peleg S, Berlin S, Brass D, Keren-Raifman T, Dessauer CW, Ivanina T, Dascal N., J Physiol. July 15, 2009; 587 (Pt 14): 3473-91.

Pregnenolone sulfate potentiates the inwardly rectifying K channel Kir2.3., Kobayashi T, Washiyama K, Ikeda K., PLoS One. July 21, 2009; 4 (7): e6311.              

Identification of the structural determinant responsible for the phosphorylation of G-protein activated potassium channel 1 by cAMP-dependent protein kinase., Müllner C, Steinecker B, Gorischek A, Schreibmayer W., FEBS J. November 1, 2009; 276 (21): 6218-26.

Further characterization of regulation of Ca(V)2.2 by stargazin., Tselnicker I, Dascal N., Channels (Austin). January 1, 2010; 4 (5): 351-4.

G alpha(i) and G betagamma jointly regulate the conformations of a G betagamma effector, the neuronal G protein-activated K+ channel (GIRK)., Berlin S, Keren-Raifman T, Castel R, Rubinstein M, Dessauer CW, Ivanina T, Dascal N., J Biol Chem. February 26, 2010; 285 (9): 6179-85.

Inhibition of G-protein-activated inwardly rectifying K+ channels by the selective norepinephrine reuptake inhibitors atomoxetine and reboxetine., Kobayashi T, Washiyama K, Ikeda K., Neuropsychopharmacology. June 1, 2010; 35 (7): 1560-9.

Cloning and characterisation of GIRK1 variants resulting from alternative RNA editing of the KCNJ3 gene transcript in a human breast cancer cell line., Wagner V, Stadelmeyer E, Riederer M, Regitnig P, Gorischek A, Devaney T, Schmidt K, Tritthart HA, Hirschberg K, Bauernhofer T, Schreibmayer W., J Cell Biochem. June 1, 2010; 110 (3): 598-608.

Trace amines depress D(2)-autoreceptor-mediated responses on midbrain dopaminergic cells., Ledonne A, Federici M, Giustizieri M, Pessia M, Imbrici P, Millan MJ, Bernardi G, Mercuri NB., Br J Pharmacol. July 1, 2010; 160 (6): 1509-20.

Actions of the prototypical 5-HT1A receptor agonist 8-OH-DPAT at human alpha2-adrenoceptors: (+)8-OH-DPAT, but not (-)8-OH-DPAT is an alpha2B subtype preferential agonist., Heusler P, Rauly-Lestienne I, Tourette A, Tardif S, Ailhaud MC, Croville G, Cussac D., Eur J Pharmacol. August 25, 2010; 640 (1-3): 8-14.

Identification and characterization of Cs(+) -permeable K(+) channel current in mouse cerebellar Purkinje cells in lobules 9 and 10 evoked by molecular layer stimulation., Ishii H, Nakajo K, Yanagawa Y, Kubo Y., Eur J Neurosci. September 1, 2010; 32 (5): 736-48.

Intron 4 containing novel GABAB1 isoforms impair GABAB receptor function., Lee C, Lee C, Mayfield RD, Harris RA., PLoS One. November 16, 2010; 5 (11): e14044.            

Gating of a G protein-sensitive mammalian Kir3.1 prokaryotic Kir channel chimera in planar lipid bilayers., Leal-Pinto E, Gómez-Llorente Y, Sundaram S, Tang QY, Ivanova-Nikolova T, Mahajan R, Baki L, Zhang Z, Chavez J, Ubarretxena-Belandia I, Logothetis DE., J Biol Chem. December 17, 2010; 285 (51): 39790-800.

G protein {beta}{gamma} gating confers volatile anesthetic inhibition to Kir3 channels., Styer AM, Mirshahi UL, Wang C, Girard L, Jin T, Logothetis DE, Mirshahi T., J Biol Chem. December 31, 2010; 285 (53): 41290-9.

Agonist-specific voltage sensitivity at the dopamine D2S receptor--molecular determinants and relevance to therapeutic ligands., Sahlholm K, Barchad-Avitzur O, Marcellino D, Gómez-Soler M, Fuxe K, Ciruela F, Arhem P., Neuropharmacology. January 1, 2011; 61 (5-6): 937-49.

Four and a half LIM protein 1C (FHL1C): a binding partner for voltage-gated potassium channel K(v1.5)., Poparic I, Schreibmayer W, Schoser B, Desoye G, Gorischek A, Miedl H, Hochmeister S, Binder J, Quasthoff S, Wagner K, Windpassinger C, Malle E., PLoS One. January 1, 2011; 6 (10): e26524.            

Inhibition of G protein-activated inwardly rectifying K+ channels by different classes of antidepressants., Kobayashi T, Washiyama K, Ikeda K., PLoS One. January 1, 2011; 6 (12): e28208.            

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