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

Papers associated with kcnj3



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Molecular cloning and characterization of a novel splicing variant of the Kir3.2 subunit predominantly expressed in mouse testis., Inanobe A, Horio Y, Fujita A, Tanemoto M, Hibino H, Inageda K, Kurachi Y., J Physiol. November 15, 1999; 521 Pt 1 19-30.

Calcium sensing properties of the GABA(B) receptor., Wise A, Green A, Main MJ, Wilson R, Fraser N, Marshall FH., Neuropharmacology. November 1, 1999; 38 (11): 1647-56.

Molecular mechanism for sodium-dependent activation of G protein-gated K+ channels., Ho IH, Murrell-Lagnado RD., J Physiol. November 1, 1999; 520 Pt 3 645-51.

Reverse physiology in drosophila: identification of a novel allatostatin-like neuropeptide and its cognate receptor structurally related to the mammalian somatostatin/galanin/opioid receptor family., Birgül N, Weise C, Kreienkamp HJ, Richter D., EMBO J. November 1, 1999; 18 (21): 5892-900.

Synergistic activation of G protein-gated inwardly rectifying potassium channels by the betagamma subunits of G proteins and Na(+) and Mg(2+) ions., Petit-Jacques J, Sui JL, Logothetis DE., J Gen Physiol. November 1, 1999; 114 (5): 673-84.                

Cannabinoid receptors can activate and inhibit G protein-coupled inwardly rectifying potassium channels in a xenopus oocyte expression system., McAllister SD, Griffin G, Satin LS, Abood ME., J Pharmacol Exp Ther. November 1, 1999; 291 (2): 618-26.

Mechanisms of inward-rectifier K+ channel inhibition by tertiapin-Q., Jin W, Klem AM, Lewis JH, Lu Z., Biochemistry. October 26, 1999; 38 (43): 14294-301.

Synthesis of a stable form of tertiapin: a high-affinity inhibitor for inward-rectifier K+ channels., Jin W, Lu Z., Biochemistry. October 26, 1999; 38 (43): 14286-93.

The inwardly rectifying K(+) channel subunit GIRK1 rescues the GIRK2 weaver phenotype., Hou P, Yan S, Tang W, Nelson DJ., J Neurosci. October 1, 1999; 19 (19): 8327-36.

Identification of melanin concentrating hormone (MCH) as the natural ligand for the orphan somatostatin-like receptor 1 (SLC-1)., Bächner D, Kreienkamp H, Weise C, Buck F, Richter D., FEBS Lett. September 3, 1999; 457 (3): 522-4.

Agonist-dependent desensitization of the kappa opioid receptor by G protein receptor kinase and beta-arrestin., Appleyard SM, Celver J, Pineda V, Kovoor A, Wayman GA, Chavkin C., J Biol Chem. August 20, 1999; 274 (34): 23802-7.

DmGluRA, a Drosophila metabotropic glutamate receptor, activates G-protein inwardly rectifying potassium channels in Xenopus oocytes., Raymond V, Hamon A, Grau Y, Lapied B., Neurosci Lett. July 2, 1999; 269 (1): 1-4.

Bombesin receptors inhibit G protein-coupled inwardly rectifying K+ channels expressed in Xenopus oocytes through a protein kinase C-dependent pathway., Stevens EB, Shah BS, Pinnock RD, Lee K., Mol Pharmacol. June 1, 1999; 55 (6): 1020-7.

New roles for RGS2, 5 and 8 on the ratio-dependent modulation of recombinant GIRK channels expressed in Xenopus oocytes., Herlitze S, Ruppersberg JP, Mark MD., J Physiol. June 1, 1999; 517 ( Pt 2) 341-52.

Functional expression and characterization of G-protein-gated inwardly rectifying K+ channels containing GIRK3., Jelacic TM, Sims SM, Clapham DE., J Membr Biol. May 15, 1999; 169 (2): 123-9.

Distinct domains of the CB1 cannabinoid receptor mediate desensitization and internalization., Jin W, Brown S, Roche JP, Hsieh C, Celver JP, Kovoor A, Chavkin C, Mackie K., J Neurosci. May 15, 1999; 19 (10): 3773-80.

Effect of extracellular cations on the inward rectifying K+ channels Kir2.1 and Kir3.1/Kir3.4., Owen JM, Quinn CC, Leach R, Findlay JB, Boyett MR., Exp Physiol. May 1, 1999; 84 (3): 471-88.

RGS7 and RGS8 differentially accelerate G protein-mediated modulation of K+ currents., Saitoh O, Kubo Y, Odagiri M, Ichikawa M, Yamagata K, Sekine T., J Biol Chem. April 2, 1999; 274 (14): 9899-904.

Molecular determinants for sodium-dependent activation of G protein-gated K+ channels., Ho IH, Murrell-Lagnado RD., J Biol Chem. March 26, 1999; 274 (13): 8639-48.

The cardiac acetylcholine-activated, inwardly rectifying K+-channel subunit GIRK1 gives rise to an inward current induced by free oxygen radicals., Jeglitsch G, Ramos P, Encabo A, Tritthart HA, Esterbauer H, Groschner K, Schreibmayer W., Free Radic Biol Med. February 1, 1999; 26 (3-4): 253-9.

Coupling of the expressed cannabinoid CB1 and CB2 receptors to phospholipase C and G protein-coupled inwardly rectifying K+ channels., Ho BY, Uezono Y, Takada S, Takase I, Izumi F., Recept Channels. January 1, 1999; 6 (5): 363-74.

Cloning and expression of a G protein-linked acetylcholine receptor from Caenorhabditis elegans., Lee YS, Park YS, Chang DJ, Hwang JM, Min CK, Kaang BK, Cho NJ., J Neurochem. January 1, 1999; 72 (1): 58-65.

GABA(B) receptors function as a heteromeric assembly of the subunits GABA(B)R1 and GABA(B)R2., Jones KA, Borowsky B, Tamm JA, Craig DA, Durkin MM, Dai M, Yao WJ, Johnson M, Gunwaldsen C, Huang LY, Tang C, Shen Q, Salon JA, Morse K, Laz T, Smith KE, Nagarathnam D, Noble SA, Branchek TA, Gerald C., Nature. December 17, 1998; 396 (6712): 674-9.

The CGRP receptor can couple via pertussis toxin sensitive and insensitive G proteins., Main MJ, Brown J, Brown S, Fraser NJ, Foord SM., FEBS Lett. December 11, 1998; 441 (1): 6-10.

Endomorphins fully activate a cloned human mu opioid receptor., Gong J, Strong JA, Zhang S, Yue X, DeHaven RN, Daubert JD, Cassel JA, Yu G, Mansson E, Yu L., FEBS Lett. November 13, 1998; 439 (1-2): 152-6.

Agonist induced homologous desensitization of mu-opioid receptors mediated by G protein-coupled receptor kinases is dependent on agonist efficacy., Kovoor A, Celver JP, Wu A, Chavkin C., Mol Pharmacol. October 1, 1998; 54 (4): 704-11.

A novel high-affinity inhibitor for inward-rectifier K+ channels., Jin W, Lu Z., Biochemistry. September 22, 1998; 37 (38): 13291-9.

Cloned human and rat galanin GALR3 receptors. Pharmacology and activation of G-protein inwardly rectifying K+ channels., Smith KE, Walker MW, Artymyshyn R, Bard J, Borowsky B, Tamm JA, Yao WJ, Vaysse PJ, Branchek TA, Gerald C, Jones KA., J Biol Chem. September 4, 1998; 273 (36): 23321-6.

Asymmetrical contributions of subunit pore regions to ion selectivity in an inward rectifier K+ channel., Silverman SK, Lester HA, Dougherty DA., Biophys J. September 1, 1998; 75 (3): 1330-9.

Human D2 and D4 dopamine receptors couple through betagamma G-protein subunits to inwardly rectifying K+ channels (GIRK1) in a Xenopus oocyte expression system: selective antagonism by L-741,626 and L-745,870 respectively., Pillai G, Brown NA, McAllister G, Milligan G, Seabrook GR., Neuropharmacology. August 1, 1998; 37 (8): 983-7.

Agonist-independent inactivation and agonist-induced desensitization of the G protein-activated K+ channel (GIRK) in Xenopus oocytes., Vorobiov D, Levin G, Lotan I, Dascal N., Pflugers Arch. June 1, 1998; 436 (1): 56-68.

Activation of inwardly rectifying K+ channels by GABA-B receptors expressed in Xenopus oocytes., Uezono Y, Akihara M, Kaibara M, Kawano C, Shibuya I, Ueda Y, Yanagihara N, Toyohira Y, Yamashita H, Taniyama K, Izumi F., Neuroreport. March 9, 1998; 9 (4): 583-7.

Direct activation of inward rectifier potassium channels by PIP2 and its stabilization by Gbetagamma., Huang CL, Feng S, Hilgemann DW., Nature. February 19, 1998; 391 (6669): 803-6.

Effects of clozapine on the delta- and kappa-opioid receptors and the G-protein-activated K+ (GIRK) channel expressed in Xenopus oocytes., Kobayashi T, Ikeda K, Kumanishi T., Br J Pharmacol. February 1, 1998; 123 (3): 421-6.

Regulation of K+ and Ca++ channels by a family of neuropeptide Y receptors., Sun L, Philipson LH, Miller RJ., J Pharmacol Exp Ther. February 1, 1998; 284 (2): 625-32.

Ion permeation through a G-protein activated (GIRK1/GIRK5) inwardly rectifying potassium channel., Luchian T, Schreibmayer W., Biochim Biophys Acta. January 19, 1998; 1368 (2): 167-70.

Mechanosensitivity of the cardiac muscarinic potassium channel. A novel property conferred by Kir3.4 subunit., Ji S, John SA, Lu Y, Weiss JN., J Biol Chem. January 16, 1998; 273 (3): 1324-8.

In vivo incorporation of unnatural amino acids into ion channels in Xenopus oocyte expression system., Nowak MW, Gallivan JP, Silverman SK, Labarca CG, Dougherty DA, Lester HA., Methods Enzymol. January 1, 1998; 293 504-29.

Probing the G-protein regulation of GIRK1 and GIRK4, the two subunits of the KACh channel, using functional homomeric mutants., Vivaudou M, Chan KW, Sui JL, Jan LY, Reuveny E, Logothetis DE., J Biol Chem. December 12, 1997; 272 (50): 31553-60.

Coupling of rat somatostatin receptor subtypes to a G-protein gated inwardly rectifying potassium channel (GIRK1)., Kreienkamp HJ, Hönck HH, Richter D., FEBS Lett. December 8, 1997; 419 (1): 92-4.

RGS8 accelerates G-protein-mediated modulation of K+ currents., Saitoh O, Kubo Y, Miyatani Y, Asano T, Nakata H., Nature. December 4, 1997; 390 (6659): 525-9.

A C-terminal peptide of the GIRK1 subunit directly blocks the G protein-activated K+ channel (GIRK) expressed in Xenopus oocytes., Luchian T, Dascal N, Dessauer C, Platzer D, Davidson N, Lester HA, Schreibmayer W., J Physiol. November 15, 1997; 505 ( Pt 1) 13-22.

Mu and delta opioid receptors are differentially desensitized by the coexpression of beta-adrenergic receptor kinase 2 and beta-arrestin 2 in xenopus oocytes., Kovoor A, Nappey V, Kieffer BL, Chavkin C., J Biol Chem. October 31, 1997; 272 (44): 27605-11.

Defective gamma-aminobutyric acid type B receptor-activated inwardly rectifying K+ currents in cerebellar granule cells isolated from weaver and Girk2 null mutant mice., Slesinger PA, Stoffel M, Jan YN, Jan LY., Proc Natl Acad Sci U S A. October 28, 1997; 94 (22): 12210-7.

RGS proteins reconstitute the rapid gating kinetics of gbetagamma-activated inwardly rectifying K+ channels., Doupnik CA, Davidson N, Lester HA, Kofuji P., Proc Natl Acad Sci U S A. September 16, 1997; 94 (19): 10461-6.

Identification of regions that regulate the expression and activity of G protein-gated inward rectifier K+ channels in Xenopus oocytes., Stevens EB, Woodward R, Ho IH, Murrell-Lagnado R., J Physiol. September 15, 1997; 503 ( Pt 3) 547-62.

Opioid receptors from a lower vertebrate (Catostomus commersoni): sequence, pharmacology, coupling to a G-protein-gated inward-rectifying potassium channel (GIRK1), and evolution., Darlison MG, Greten FR, Harvey RJ, Kreienkamp HJ, Stühmer T, Zwiers H, Lederis K, Richter D., Proc Natl Acad Sci U S A. July 22, 1997; 94 (15): 8214-9.

Activation of heteromeric G protein-gated inward rectifier K+ channels overexpressed by adenovirus gene transfer inhibits the excitability of hippocampal neurons., Ehrengruber MU, Doupnik CA, Xu Y, Xu Y, Garvey J, Jasek MC, Lester HA, Davidson N., Proc Natl Acad Sci U S A. June 24, 1997; 94 (13): 7070-5.

Cloning and characterization of Kir3.1 (GIRK1) C-terminal alternative splice variants., Nelson CS, Marino JL, Allen CN., Brain Res Mol Brain Res. June 1, 1997; 46 (1-2): 185-96.

Molecular determinants for assembly of G-protein-activated inwardly rectifying K+ channels., Woodward R, Stevens EB, Murrell-Lagnado RD., J Biol Chem. April 18, 1997; 272 (16): 10823-30.

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