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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.
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.
Time resolved kinetics of direct G beta 1 gamma 2 interactions with the carboxyl terminus of Kir3.4 inward rectifier K+ channel subunits. , Doupnik CA, Dessauer CW, Slepak VZ, Gilman AG, Davidson N, Lester HA., Neuropharmacology. January 1, 1996; 35 (7): 923-31.
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.
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 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.
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.
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.
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.
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.
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.
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.
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.
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.
A regenerative link in the ionic fluxes through the weaver potassium channel underlies the pathophysiology of the mutation. , Silverman SK, Kofuji P, Dougherty DA, Davidson N, Lester HA., Proc Natl Acad Sci U S A. December 24, 1996; 93 (26): 15429-34.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Activation of inwardly rectifying K+ channels by distinct PtdIns(4,5)P2 interactions. , Zhang H , He C, Yan X, Mirshahi T, Logothetis DE., Nat Cell Biol. July 1, 1999; 1 (3): 183-8.
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.
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.
Distinct specificities of inwardly rectifying K(+) channels for phosphoinositides. , Rohács T, Chen J , Prestwich GD, Logothetis DE., J Biol Chem. December 17, 1999; 274 (51): 36065-72.
Inhibition by various antipsychotic drugs of the G-protein-activated inwardly rectifying K(+) ( GIRK) channels expressed in xenopus oocytes. , Kobayashi T, Ikeda K, Kumanishi T., Br J Pharmacol. April 1, 2000; 129 (8): 1716-22.
Slow modal gating of single G protein-activated K+ channels expressed in Xenopus oocytes. , Yakubovich D, Pastushenko V, Bitler A, Dessauer CW, Dascal N ., J Physiol. May 1, 2000; 524 Pt 3 737-55.
Heterologous facilitation of G protein-activated K(+) channels by beta-adrenergic stimulation via cAMP-dependent protein kinase. , Müllner C, Vorobiov D, Bera AK, Uezono Y, Yakubovich D, Frohnwieser-Steinecker B, Dascal N , Schreibmayer W., J Gen Physiol. May 1, 2000; 115 (5): 547-58.
TrkB activation by brain-derived neurotrophic factor inhibits the G protein-gated inward rectifier Kir3 by tyrosine phosphorylation of the channel. , Rogalski SL, Appleyard SM, Pattillo A, Terman GW, Chavkin C., J Biol Chem. August 18, 2000; 275 (33): 25082-8.
Cs+ block of the cardiac muscarinic K+ channel, GIRK1/ GIRK4, is not dependent on the aspartate residue at position 173. , Dibb KM, Leach R, Lancaster MK, Findlay JB, Boyett MR., Pflugers Arch. September 1, 2000; 440 (5): 740-4.
G-protein mediated gating of inward-rectifier K+ channels. , Mark MD, Herlitze S., Eur J Biochem. October 1, 2000; 267 (19): 5830-6.
Single channel studies of inward rectifier potassium channel regulation by muscarinic acetylcholine receptors. , Bard J, Kunkel MT, Peralta EG., J Gen Physiol. November 1, 2000; 116 (5): 645-52.
Residues and mechanisms for slow activation and Ba2+ block of the cardiac muscarinic K+ channel, Kir3.1/ Kir3.4. , Lancaster MK, Dibb KM, Quinn CC, Leach R, Lee JK , Lee JK , Findlay JB, Boyett MR., J Biol Chem. November 17, 2000; 275 (46): 35831-9.
Inhibition of a Gi-activated potassium channel ( GIRK1/4) by the Gq-coupled m1 muscarinic acetylcholine receptor. , Hill JJ, Peralta EG., J Biol Chem. February 23, 2001; 276 (8): 5505-10.
Identification of G protein-coupled, inward rectifier potassium channel gene products from the rat anterior pituitary gland. , Gregerson KA, Flagg TP, O'Neill TJ, Anderson M, Lauring O, Horel JS, Welling PA., Endocrinology. July 1, 2001; 142 (7): 2820-32.
G protein-gated inwardly rectifying potassium channels are targets for volatile anesthetics. , Weigl LG, Schreibmayer W., Mol Pharmacol. August 1, 2001; 60 (2): 282-9.
Gbeta residues that do not interact with Galpha underlie agonist-independent activity of K+ channels. , Mirshahi T, Robillard L, Zhang H , Hébert TE, Logothetis DE., J Biol Chem. March 1, 2002; 277 (9): 7348-55.
Functional expression of a novel ginsenoside Rf binding protein from rat brain mRNA in Xenopus laevis oocytes. , Choi S, Jung SY, Ko YS, Koh SR, Rhim H, Nah SY., Mol Pharmacol. April 1, 2002; 61 (4): 928-35.