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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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Functional coupling of the nociceptin/orphanin FQ receptor with the G-protein-activated K+ (GIRK) channel., Ikeda K, Kobayashi K, Kobayashi T, Ichikawa T, Kumanishi T, Kishida H, Yano R, Manabe T., Brain Res Mol Brain Res. April 1, 1997; 45 (1): 117-26.


Positive and negative coupling of the metabotropic glutamate receptors to a G protein-activated K+ channel, GIRK, in Xenopus oocytes., Sharon D, Vorobiov D, Dascal N., J Gen Physiol. April 1, 1997; 109 (4): 477-90.        


Specific regions of heteromeric subunits involved in enhancement of G protein-gated K+ channel activity., Chan KW, Sui JL, Vivaudou M, Logothetis DE., J Biol Chem. March 7, 1997; 272 (10): 6548-55.


Effects of sigma ligands on the nociceptin/orphanin FQ receptor co-expressed with the G-protein-activated K+ channel in Xenopus oocytes., Kobayashi T, Ikeda K, Togashi S, Itoh N, Kumanishi T., Br J Pharmacol. March 1, 1997; 120 (6): 986-7.


Inwardly rectifying potassium channels: their molecular heterogeneity and function., Isomoto S, Kondo C, Kurachi Y., Jpn J Physiol. February 1, 1997; 47 (1): 11-39.


Subunit interactions in the assembly of neuronal Kir3.0 inwardly rectifying K+ channels., Döring F, Wischmeyer E, Spauschus A, Thomzig A, Veh R, Karschin A., Mol Cell Neurosci. January 1, 1997; 9 (3): 194-206.


ATP-dependent regulation of a G protein-coupled K+ channel (GIRK1/GIRK4) expressed in oocytes., Kim D, Watson M, Indyk V., Am J Physiol. January 1, 1997; 272 (1 Pt 2): H195-206.


Subunit stoichiometry of a heteromultimeric G protein-coupled inward-rectifier K+ channel., Silverman SK, Lester HA, Dougherty DA., J Biol Chem. November 29, 1996; 271 (48): 30524-8.


Control of channel activity through a unique amino acid residue of a G protein-gated inwardly rectifying K+ channel subunit., Chan KW, Sui JL, Vivaudou M, Logothetis DE., Proc Natl Acad Sci U S A. November 26, 1996; 93 (24): 14193-8.


Na+ activation of the muscarinic K+ channel by a G-protein-independent mechanism., Sui JL, Chan KW, Logothetis DE., J Gen Physiol. November 1, 1996; 108 (5): 381-91.


Identification of domains of the cardiac inward rectifying K+ channel, CIR, involved in the heteromultimer formation and in the G-protein gating., Kubo Y, Iizuka M., Biochem Biophys Res Commun. October 3, 1996; 227 (1): 240-7.


Metabotropic glutamate receptors activate G-protein-coupled inwardly rectifying potassium channels in Xenopus oocytes., Saugstad JA, Segerson TP, Westbrook GL., J Neurosci. October 1, 1996; 16 (19): 5979-85.


Effects of sigma ligands on the cloned mu-, delta- and kappa-opioid receptors co-expressed with G-protein-activated K+ (GIRK) channel in Xenopus oocytes., Kobayashi T, Ikeda K, Ichikawa T, Togashi S, Kumanishi T., Br J Pharmacol. September 1, 1996; 119 (1): 73-80.


Functional selectivity of orphanin FQ for its receptor coexpressed with potassium channel subunits in Xenopus laevis oocytes., Matthes H, Seward EP, Kieffer B, North RA., Mol Pharmacol. September 1, 1996; 50 (3): 447-50.


The weaver mutation changes the ion selectivity of the affected inwardly rectifying potassium channel GIRK2., Tong Y, Wei J, Zhang S, Strong JA, Dlouhy SR, Hodes ME, Ghetti B, Yu L., FEBS Lett. July 15, 1996; 390 (1): 63-8.


Cloning of a G protein-activated inwardly rectifying potassium channel from human cerebellum., Schoots O, Yue KT, MacDonald JF, Hampson DR, Nobrega JN, Dixon LM, Van Tol HH., Brain Res Mol Brain Res. July 1, 1996; 39 (1-2): 23-30.


Functional expression and cellular mRNA localization of a G protein-activated K+ inward rectifier isolated from rat brain., Dissmann E, Wischmeyer E, Spauschus A, Pfeil DV, Karschin C, Karschin A., Biochem Biophys Res Commun. June 14, 1996; 223 (2): 474-9.


Mutation of a conserved serine in TM4 of opioid receptors confers full agonistic properties to classical antagonists., Claude PA, Wotta DR, Zhang XH, Prather PL, McGinn TM, Erickson LJ, Loh HH, Law PY., Proc Natl Acad Sci U S A. June 11, 1996; 93 (12): 5715-9.


Inhibition of an inwardly rectifying K+ channel by G-protein alpha-subunits., Schreibmayer W, Dessauer CW, Vorobiov D, Gilman AG, Lester HA, Davidson N, Dascal N., Nature. April 18, 1996; 380 (6575): 624-7.


D2, D3, and D4 dopamine receptors couple to G protein-regulated potassium channels in Xenopus oocytes., Werner P, Hussy N, Buell G, Jones KA, North RA., Mol Pharmacol. April 1, 1996; 49 (4): 656-61.


Specificity of coupling of muscarinic receptor isoforms to a novel chick inward-rectifying acetylcholine-sensitive K+ channel., Gadbut AP, Riccardi D, Wu L, Hebert SC, Galper JB., J Biol Chem. March 15, 1996; 271 (11): 6398-402.


A recombinant inwardly rectifying potassium channel coupled to GTP-binding proteins., Chan KW, Langan MN, Sui JL, Kozak JA, Pabon A, Ladias JA, Logothetis DE., J Gen Physiol. March 1, 1996; 107 (3): 381-97.


Coexpression with potassium channel subunits used to clone the Y2 receptor for neuropeptide Y., Rimland JM, Seward EP, Humbert Y, Ratti E, Trist DG, North RA., Mol Pharmacol. March 1, 1996; 49 (3): 387-90.


Cloning of a Xenopus laevis inwardly rectifying K+ channel subunit that permits GIRK1 expression of IKACh currents in oocytes., Hedin KE, Lim NF, Clapham DE., Neuron. February 1, 1996; 16 (2): 423-9.


Functional effects of the mouse weaver mutation on G protein-gated inwardly rectifying K+ channels., Slesinger PA, Patil N, Liao YJ, Jan YN, Jan LY, Cox DR., Neuron. February 1, 1996; 16 (2): 321-31.


A unique P-region residue is required for slow voltage-dependent gating of a G protein-activated inward rectifier K+ channel expressed in Xenopus oocytes., Kofuji P, Doupnik CA, Davidson N, Lester HA., J Physiol. February 1, 1996; 490 ( Pt 3) 633-45.


A G-protein-activated inwardly rectifying K+ channel (GIRK4) from human hippocampus associates with other GIRK channels., Spauschus A, Lentes KU, Wischmeyer E, Dissmann E, Karschin C, Karschin A., J Neurosci. February 1, 1996; 16 (3): 930-8.


The K+ channel inward rectifier subunits form a channel similar to neuronal G protein-gated K+ channel., Velimirovic BM, Gordon EA, Lim NF, Navarro B, Clapham DE., FEBS Lett. January 22, 1996; 379 (1): 31-7.


A novel ubiquitously distributed isoform of GIRK2 (GIRK2B) enhances GIRK1 expression of the G-protein-gated K+ current in Xenopus oocytes., Isomoto S, Kondo C, Takahashi N, Matsumoto S, Yamada M, Takumi T, Horio Y, Kurachi Y., Biochem Biophys Res Commun. January 5, 1996; 218 (1): 286-91.


Localization and interaction of epitope-tagged GIRK1 and CIR inward rectifier K+ channel subunits., Kennedy ME, Nemec J, Clapham DE., Neuropharmacology. January 1, 1996; 35 (7): 831-9.


Molecular properties of neuronal G-protein-activated inwardly rectifying K+ channels., Lesage F, Guillemare E, Fink M, Duprat F, Heurteaux C, Fosset M, Romey G, Barhanin J, Lazdunski M., J Biol Chem. December 1, 1995; 270 (48): 28660-7.


Identification of domains conferring G protein regulation on inward rectifier potassium channels., Kunkel MT, Peralta EG., Cell. November 3, 1995; 83 (3): 443-9.


Pancreatic islet cells express a family of inwardly rectifying K+ channel subunits which interact to form G-protein-activated channels., Ferrer J, Nichols CG, Makhina EN, Salkoff L, Bernstein J, Gerhard D, Wasson J, Ramanadham S, Permutt A., J Biol Chem. November 3, 1995; 270 (44): 26086-91.


Involvement of G-protein alpha il subunits in activation of G-protein gated inward rectifying K+ channels (GIRK1) by human NPY1 receptors., Brown NA, McAllister G, Weinberg D, Milligan G, Seabrook GR., Br J Pharmacol. November 1, 1995; 116 (5): 2346-8.


Identification of structural elements involved in G protein gating of the GIRK1 potassium channel., Slesinger PA, Reuveny E, Jan YN, Jan LY., Neuron. November 1, 1995; 15 (5): 1145-56.


Evidence that direct binding of G beta gamma to the GIRK1 G protein-gated inwardly rectifying K+ channel is important for channel activation., Huang CL, Slesinger PA, Casey PJ, Jan YN, Jan LY., Neuron. November 1, 1995; 15 (5): 1133-43.


Inhibition of function in Xenopus oocytes of the inwardly rectifying G-protein-activated atrial K channel (GIRK1) by overexpression of a membrane-attached form of the C-terminal tail., Dascal N, Doupnik CA, Ivanina T, Bausch S, Wang W, Lin C, Garvey J, Chavkin C, Lester HA, Davidson N., Proc Natl Acad Sci U S A. July 18, 1995; 92 (15): 6758-62.


Heterologous multimeric assembly is essential for K+ channel activity of neuronal and cardiac G-protein-activated inward rectifiers., Duprat F, Lesage F, Guillemare E, Fink M, Hugnot JP, Bigay J, Lazdunski M, Romey G, Barhanin J., Biochem Biophys Res Commun. July 17, 1995; 212 (2): 657-63.


Evidence that neuronal G-protein-gated inwardly rectifying K+ channels are activated by G beta gamma subunits and function as heteromultimers., Kofuji P, Davidson N, Lester HA., Proc Natl Acad Sci U S A. July 3, 1995; 92 (14): 6542-6.


Intrinsic gating properties of a cloned G protein-activated inward rectifier K+ channel., Doupnik CA, Lim NF, Kofuji P, Davidson N, Lester HA., J Gen Physiol. July 1, 1995; 106 (1): 1-23.


Cloning and functional characterization of a novel ATP-sensitive potassium channel ubiquitously expressed in rat tissues, including pancreatic islets, pituitary, skeletal muscle, and heart., Inagaki N, Tsuura Y, Namba N, Masuda K, Gonoi T, Horie M, Seino Y, Mizuta M, Seino S., J Biol Chem. March 17, 1995; 270 (11): 5691-4.


The G-protein-gated atrial K+ channel IKACh is a heteromultimer of two inwardly rectifying K(+)-channel proteins., Krapivinsky G, Gordon EA, Wickman K, Velimirović B, Krapivinsky L, Clapham DE., Nature. March 9, 1995; 374 (6518): 135-41.


Functional couplings of the delta- and the kappa-opioid receptors with the G-protein-activated K+ channel., Ikeda K, Kobayashi T, Ichikawa T, Usui H, Kumanishi T., Biochem Biophys Res Commun. March 8, 1995; 208 (1): 302-8.


A G protein-gated K channel is activated via beta 2-adrenergic receptors and G beta gamma subunits in Xenopus oocytes., Lim NF, Dascal N, Labarca C, Davidson N, Lester HA., J Gen Physiol. March 1, 1995; 105 (3): 421-39.


Kappa-opioid receptors couple to inwardly rectifying potassium channels when coexpressed by Xenopus oocytes., Henry DJ, Grandy DK, Lester HA, Davidson N, Chavkin C., Mol Pharmacol. March 1, 1995; 47 (3): 551-7.


Activation of inwardly rectifying potassium channels (GIRK1) by co-expressed rat brain cannabinoid receptors in Xenopus oocytes., Henry DJ, Chavkin C., Neurosci Lett. February 17, 1995; 186 (2-3): 91-4.


Agonist-induced desensitization of the mu opioid receptor-coupled potassium channel (GIRK1)., Kovoor A, Henry DJ, Chavkin C., J Biol Chem. January 13, 1995; 270 (2): 589-95.


Functional characterization and localization of a cardiac-type inwardly rectifying K+ channel., Iizuka M, Kubo Y, Tsunenari I, Pan CX, Akiba I, Kono T., Recept Channels. January 1, 1995; 3 (4): 299-315.


Colocalization of mu opioid receptors with GIRK1 potassium channels in the rat brain: an immunocytochemical study., Bausch SB, Patterson TA, Ehrengruber MU, Lester HA, Davidson N, Chavkin C., Recept Channels. January 1, 1995; 3 (3): 221-41.


Cloning provides evidence for a family of inward rectifier and G-protein coupled K+ channels in the brain., Lesage F, Duprat F, Fink M, Guillemare E, Coppola T, Lazdunski M, Hugnot JP., FEBS Lett. October 10, 1994; 353 (1): 37-42.

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