Papers associated with oocyte (and kcnj3)

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	Expression levels of RGS7 and RGS4 proteins determine the mode of regulation of the G protein-activated K(+) channel and control regulation of RGS7 by G beta 5., Keren-Raifman T., FEBS Lett. March 9, 2001; 492 (1-2): 20-8.
	Slow modal gating of single G protein-activated K+ channels expressed in Xenopus oocytes., Yakubovich D., 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., J Gen Physiol. May 1, 2000; 115 (5): 547-58.
	Inhibition by various antipsychotic drugs of the G-protein-activated inwardly rectifying K(+) (GIRK) channels expressed in xenopus oocytes., Kobayashi T., Br J Pharmacol. April 1, 2000; 129 (8): 1716-22.
	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., 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., J Pharmacol Exp Ther. November 1, 1999; 291 (2): 618-26.
	Agonist-dependent desensitization of the kappa opioid receptor by G protein receptor kinase and beta-arrestin., Appleyard SM., J Biol Chem. August 20, 1999; 274 (34): 23802-7.
	Distinct domains of the CB1 cannabinoid receptor mediate desensitization and internalization., Jin W., J Neurosci. May 15, 1999; 19 (10): 3773-80.
	Cloning and expression of a G protein-linked acetylcholine receptor from Caenorhabditis elegans., Lee YS., J Neurochem. January 1, 1999; 72 (1): 58-65.
	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., Neuropharmacology. August 1, 1998; 37 (8): 983-7.
	Effects of clozapine on the delta- and kappa-opioid receptors and the G-protein-activated K+ (GIRK) channel expressed in Xenopus oocytes., Kobayashi T., Br J Pharmacol. February 1, 1998; 123 (3): 421-6.
	In vivo incorporation of unnatural amino acids into ion channels in Xenopus oocyte expression system., Nowak MW., 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., J Biol Chem. December 12, 1997; 272 (50): 31553-60.
	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., J Biol Chem. October 31, 1997; 272 (44): 27605-11.
	Functional coupling of the nociceptin/orphanin FQ receptor with the G-protein-activated K+ (GIRK) channel., Ikeda K., 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., 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., J Biol Chem. March 7, 1997; 272 (10): 6548-55.
	A recombinant inwardly rectifying potassium channel coupled to GTP-binding proteins., Chan KW., J Gen Physiol. March 1, 1996; 107 (3): 381-97.
	Cloning of a Xenopus laevis inwardly rectifying K+ channel subunit that permits GIRK1 expression of IKACh currents in oocytes., Hedin KE., Neuron. February 1, 1996; 16 (2): 423-9.
	Heterologous multimeric assembly is essential for K+ channel activity of neuronal and cardiac G-protein-activated inward rectifiers., Duprat F., Biochem Biophys Res Commun. July 17, 1995; 212 (2): 657-63.

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