Papers associated with oocyte (and kcnj3)

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	Dopamine-induced arrestin recruitment and desensitization of the dopamine D4 receptor is regulated by G protein-coupled receptor kinase-2., Burström V., Front Pharmacol. January 1, 2023; 14 1087171.
	The activity of the serotonergic 5-HT1A receptor is modulated by voltage and sodium levels., Tauber M., J Biol Chem. June 1, 2022; 298 (6): 101978.
	Voltage dependence of the cannabinoid CB1 receptor., Goldberger E., Front Pharmacol. January 1, 2022; 13 1022275.
	WIN55,212-2, a Dual Modulator of Cannabinoid Receptors and G Protein-Coupled Inward Rectifier Potassium Channels., An D., Biomedicines. April 28, 2021; 9 (5):
	Identification of a unique endoplasmic retention motif in the Xenopus GIRK5 channel and its contribution to oocyte maturation., Rangel-Garcia CI., FEBS Open Bio. April 1, 2021; 11 (4): 1093-1108.
	Ligand with Two Modes of Interaction with the Dopamine D2 Receptor-An Induced-Fit Mechanism of Insurmountable Antagonism., Ågren R., ACS Chem Neurosci. October 7, 2020; 11 (19): 3130-3143.
	Sodium ions allosterically modulate the M2 muscarinic receptor., Friedman S., Sci Rep. July 7, 2020; 10 (1): 11177.
	A Collision Coupling Model Governs the Activation of Neuronal GIRK1/2 Channels by Muscarinic-2 Receptors., Berlin S., Front Pharmacol. April 7, 2020; 11 1216.
	Hydrogen Sulfide Impairs Meiosis Resumption in Xenopuslaevis Oocytes., Gelaude A., Cells. January 17, 2020; 9 (1):
	The coupling of the M2 muscarinic receptor to its G protein is voltage dependent., Ben-Chaim Y., PLoS One. October 31, 2019; 14 (10): e0224367.
	A Photoswitchable Agonist for the Histamine H3 Receptor, a Prototypic Family A G-Protein-Coupled Receptor., Hauwert NJ., Angew Chem Int Ed Engl. March 26, 2019; 58 (14): 4531-4535.
	Mutual action by Gγ and Gβ for optimal activation of GIRK channels in a channel subunit-specific manner., Tabak G., Sci Rep. January 24, 2019; 9 (1): 508.
	The Beta-Arrestin-Biased Dopamine D2 Receptor Ligand, UNC9994, Is a Partial Agonist at G-Protein-Mediated Potassium Channel Activation., Ågren R., Int J Neuropsychopharmacol. December 1, 2018; 21 (12): 1102-1108.
	Point mutation of a conserved aspartate, D69, in the muscarinic M 2  receptor does not modify voltage-sensitive agonist potency., Ågren R., Biochem Biophys Res Commun. January 29, 2018; 496 (1): 101-104.
	Mechanism of Assembly and Cooperativity of Homomeric and Heteromeric Metabotropic Glutamate Receptors., Levitz J., Neuron. October 5, 2016; 92 (1): 143-159.
	A Quantitative Model of the GIRK1/2 Channel Reveals That Its Basal and Evoked Activities Are Controlled by Unequal Stoichiometry of Gα and Gβγ., Yakubovich D., PLoS Comput Biol. November 6, 2015; 11 (11): e1004598.
	RGS4 regulates partial agonism of the M2 muscarinic receptor-activated K+ currents., Chen IS., J Physiol. March 15, 2014; 592 (6): 1237-48.
	Voltage affects the dissociation rate constant of the m2 muscarinic receptor., Ben Chaim Y., PLoS One. September 3, 2013; 8 (9): e74354.
	The polarization of the G-protein activated potassium channel GIRK5 to the vegetal pole of Xenopus laevis oocytes is driven by a di-leucine motif., Díaz-Bello B., PLoS One. May 15, 2013; 8 (5): e64096.
	Molecular basis of the facilitation of the heterooligomeric GIRK1/GIRK4 complex by cAMP dependent protein kinase., Treiber F., Biochim Biophys Acta. April 1, 2013; 1828 (4): 1214-21.
	RGS proteins maintain robustness of GPCR-GIRK coupling by selective stimulation of the G protein subunit Gαo., Chuang HH., Sci Signal. February 21, 2012; 5 (212): ra15.
	Engineering of an artificial light-modulated potassium channel., Caro LN., PLoS One. January 1, 2012; 7 (8): e43766.
	Discovery, characterization, and structure-activity relationships of an inhibitor of inward rectifier potassium (Kir) channels with preference for Kir2.3, Kir3.x, and Kir7.1., Raphemot R., Front Pharmacol. November 30, 2011; 2 75.
	β2-Adrenergic ion-channel coupled receptors as conformational motion detectors., Caro LN., PLoS One. March 9, 2011; 6 (3): e18226.
	Inhibition of g protein-activated inwardly rectifying k channels by phencyclidine., Kobayashi T., Curr Neuropharmacol. March 1, 2011; 9 (1): 244-6.
	Identification of selective agonists and antagonists to g protein-activated inwardly rectifying potassium channels: candidate medicines for drug dependence and pain., Nishizawa D., Curr Neuropharmacol. March 1, 2011; 9 (1): 113-7.
	Inhibition of G protein-activated inwardly rectifying K+ channels by different classes of antidepressants., Kobayashi T., PLoS One. January 1, 2011; 6 (12): e28208.
	Intron 4 containing novel GABAB1 isoforms impair GABAB receptor function., Lee C, Lee C., PLoS One. November 16, 2010; 5 (11): e14044.
	Inhibition of G-protein-activated inwardly rectifying K+ channels by the selective norepinephrine reuptake inhibitors atomoxetine and reboxetine., Kobayashi T., Neuropsychopharmacology. June 1, 2010; 35 (7): 1560-9.
	Pregnenolone sulfate potentiates the inwardly rectifying K channel Kir2.3., Kobayashi T., PLoS One. July 21, 2009; 4 (7): e6311.
	Inhibitory effects of the antiepileptic drug ethosuximide on G protein-activated inwardly rectifying K+ channels., Kobayashi T., Neuropharmacology. February 1, 2009; 56 (2): 499-506.
	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., Int J Neuropsychopharmacol. May 1, 2008; 11 (3): 293-307.
	Subunit stoichiometry of heterologously expressed G-protein activated inwardly rectifying potassium channels analysed by fluorescence intensity ratio measurement., Grasser E., Pflugers Arch. March 1, 2008; 455 (6): 1017-24.
	Inhibition by cocaine of G protein-activated inwardly rectifying K+ channels expressed in Xenopus oocytes., Kobayashi T., Toxicol In Vitro. June 1, 2007; 21 (4): 656-64.
	Functional activation by central monoamines of human dopamine D(4) receptor polymorphic variants coupled to GIRK channels in Xenopus oocytes., Wedemeyer C., Eur J Pharmacol. May 21, 2007; 562 (3): 165-73.
	Differential agonist and inverse agonist profile of antipsychotics at D2L receptors coupled to GIRK potassium channels., Heusler P., Neuropharmacology. March 1, 2007; 52 (4): 1106-13.
	Testosterone and progesterone rapidly attenuate plasma membrane Gbetagamma-mediated signaling in Xenopus laevis oocytes by signaling through classical steroid receptors., Evaul K., Mol Endocrinol. January 1, 2007; 21 (1): 186-96.
	Inhibition of G protein-activated inwardly rectifying K+ channels by the antidepressant paroxetine., Kobayashi T., J Pharmacol Sci. November 1, 2006; 102 (3): 278-87.
	Inhibition of G protein-activated inwardly rectifying K+ channels by ifenprodil., Kobayashi T., Neuropsychopharmacology. March 1, 2006; 31 (3): 516-24.
	Tyrosine phosphorylation of K(ir)3.1 in spinal cord is induced by acute inflammation, chronic neuropathic pain, and behavioral stress., Ippolito DL., J Biol Chem. December 16, 2005; 280 (50): 41683-93.
	Effects of interferon-alpha on cloned opioid receptors expressed in Xenopus oocytes., Kobayashi T., Life Sci. December 10, 2004; 76 (4): 407-15.
	Carboxy-terminal determinants of conductance in inward-rectifier K channels., Zhang YY., J Gen Physiol. December 1, 2004; 124 (6): 729-39.
	Modulators of G protein-activated inwardly rectifying K+ channels: potentially therapeutic agents for addictive drug users., Kobayashi T., Ann N Y Acad Sci. October 1, 2004; 1025 590-4.
	beta-Funaltrexamine, a gauge for the recognition site of wildtype and mutant H297Q mu-opioid receptors., Spivak CE., Synapse. July 1, 2003; 49 (1): 55-60.
	Effects of ginsenoside on G protein-coupled inwardly rectifying K+ channel activity expressed in Xenopus oocytes., Choi S., Eur J Pharmacol. May 9, 2003; 468 (2): 83-92.
	Inhibition of G protein-activated inwardly rectifying K+ channels by fluoxetine (Prozac)., Kobayashi T., Br J Pharmacol. March 1, 2003; 138 (6): 1119-28.
	Effects of extracellular sodium on mu-opioid receptors coupled to potassium channels coexpressed in Xenopus oocytes., Oz M., Pflugers Arch. March 1, 2003; 445 (6): 716-20.
	Opioid receptor coupling to GIRK channels. In vitro studies using a Xenopus oocyte expression system and in vivo studies on weaver mutant mice., Ikeda K., Methods Mol Med. January 1, 2003; 84 53-64.
	Functional characterization of an endogenous Xenopus oocyte adenosine receptor., Kobayashi T., Br J Pharmacol. January 1, 2002; 135 (2): 313-22.
	Three functional isoforms of GAR-2, a Caenorhabditis elegans G-protein-linked acetylcholine receptor, are produced by alternative splicing., Suh SJ., Biochem Biophys Res Commun. November 16, 2001; 288 (5): 1238-43.

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