Papers associated with nerve (and kcnj3)

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	Involvement of spinal G-protein inwardly rectifying potassium (GIRK) channels in the enhanced antinociceptive effects of the activation of both μ-opioid and cannabinoid CB1 receptors., Takemura Y., J Pharmacol Sci. July 1, 2022; 149 (3): 85-92.
	Four and a half LIM protein 1C (FHL1C): a binding partner for voltage-gated potassium channel K(v1.5)., Poparic I., PLoS One. January 1, 2011; 6 (10): e26524.
	Intron 4 containing novel GABAB1 isoforms impair GABAB receptor function., Lee C, Lee C., PLoS One. November 16, 2010; 5 (11): e14044.
	Trace amines depress D(2)-autoreceptor-mediated responses on midbrain dopaminergic cells., Ledonne A., Br J Pharmacol. July 1, 2010; 160 (6): 1509-20.
	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.
	Identification of the structural determinant responsible for the phosphorylation of G-protein activated potassium channel 1 by cAMP-dependent protein kinase., Müllner C., FEBS J. November 1, 2009; 276 (21): 6218-26.
	Pregnenolone sulfate potentiates the inwardly rectifying K channel Kir2.3., Kobayashi T., PLoS One. July 21, 2009; 4 (7): e6311.
	Divergent regulation of GIRK1 and GIRK2 subunits of the neuronal G protein gated K+ channel by GalphaiGDP and Gbetagamma., Rubinstein M., J Physiol. July 15, 2009; 587 (Pt 14): 3473-91.
	Differential voltage-sensitivity of D2-like dopamine receptors., Sahlholm K., Biochem Biophys Res Commun. September 26, 2008; 374 (3): 496-501.
	Identification of peptides that inhibit regulator of G protein signaling 4 function., Wang Y., Pharmacology. January 1, 2008; 82 (2): 97-104.
	Inhibition of G protein-activated inwardly rectifying K+ channels by ifenprodil., Kobayashi T., Neuropsychopharmacology. March 1, 2006; 31 (3): 516-24.
	G protein-activated inwardly rectifying K+ channel inhibition and rescue of weaver mouse motor functions by antidepressants., Takahashi T., Neurosci Res. February 1, 2006; 54 (2): 104-11.
	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.
	Tertiapin-Q blocks recombinant and native large conductance K+ channels in a use-dependent manner., Kanjhan R., J Pharmacol Exp Ther. September 1, 2005; 314 (3): 1353-61.
	Phosphorylation of a tyrosine at the N-terminus regulates the surface expression of GIRK5 homomultimers., Mora SI., FEBS Lett. June 6, 2005; 579 (14): 3019-23.
	Gbetagamma-dependent and Gbetagamma-independent basal activity of G protein-activated K+ channels., Rishal I., J Biol Chem. April 29, 2005; 280 (17): 16685-94.
	Cytoplasmic domain structures of Kir2.1 and Kir3.1 show sites for modulating gating and rectification., Pegan S., Nat Neurosci. March 1, 2005; 8 (3): 279-87.
	Molecular cloning and characterization of a new RGS protein of Medaka., Itoh M., Gene. January 31, 2005; 345 (2): 165-71.
	RFamide-related peptides signal through the neuropeptide FF receptor and regulate pain-related responses in the rat., Pertovaara A., Neuroscience. January 1, 2005; 134 (3): 1023-32.
	Kinetic modeling of Na(+)-induced, Gbetagamma-dependent activation of G protein-gated K(+) channels., Yakubovich D., J Mol Neurosci. January 1, 2005; 25 (1): 7-19.
	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.
	K+ activation of kir3.1/kir3.4 and kv1.4 K+ channels is regulated by extracellular charges., Claydon TW., Biophys J. October 1, 2004; 87 (4): 2407-18.
	Inhibition of G protein-activated inwardly rectifying K+ channels by various antidepressant drugs., Kobayashi T., Neuropsychopharmacology. October 1, 2004; 29 (10): 1841-51.
	The sensitivity of G protein-activated K+ channels toward halothane is essentially determined by the C terminus., Milovic S., J Biol Chem. August 13, 2004; 279 (33): 34240-9.
	Gbetagamma-activated inwardly rectifying K(+) (GIRK) channel activation kinetics via Galphai and Galphao-coupled receptors are determined by Galpha-specific interdomain interactions that affect GDP release rates., Zhang Q., J Biol Chem. July 9, 2004; 279 (28): 29787-96.
	A retinal-specific regulator of G-protein signaling interacts with Galpha(o) and accelerates an expressed metabotropic glutamate receptor 6 cascade., Dhingra A., J Neurosci. June 23, 2004; 24 (25): 5684-93.
	Molecular determinants responsible for differential cellular distribution of G protein-gated inwardly rectifying K+ channels., Mirshahi T., J Biol Chem. March 19, 2004; 279 (12): 11890-7.
	betaL-betaM loop in the C-terminal domain of G protein-activated inwardly rectifying K(+) channels is important for G(betagamma) subunit activation., Finley M., J Physiol. March 16, 2004; 555 (Pt 3): 643-57.
	Molecular basis for the inhibition of G protein-coupled inward rectifier K(+) channels by protein kinase C., Mao J., Proc Natl Acad Sci U S A. January 27, 2004; 101 (4): 1087-92.
	The selectivity filter may act as the agonist-activated gate in the G protein-activated Kir3.1/Kir3.4 K+ channel., Claydon TW., J Biol Chem. December 12, 2003; 278 (50): 50654-63.
	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.
	Serine 329 of the mu-opioid receptor interacts differently with agonists., Pil J., J Pharmacol Exp Ther. March 1, 2003; 304 (3): 924-30.
	Inhibition of G-protein-coupled inward rectifying K+ channels by intracellular acidosis., Mao J., J Biol Chem. February 28, 2003; 278 (9): 7091-8.
	Gating properties of GIRK channels activated by Galpha(o)- and Galpha(i)-coupled muscarinic m2 receptors in Xenopus oocytes: the role of receptor precoupling in RGS modulation., Zhang Q., J Physiol. December 1, 2002; 545 (2): 355-73.
	Early embryonic expression of ion channels and pumps in chick and Xenopus development., Rutenberg J., Dev Dyn. December 1, 2002; 225 (4): 469-84.
	Activation of the cloned muscarinic potassium channel by G protein beta gamma subunits., Reuveny E., Nature. July 14, 1994; 370 (6485): 143-6.
	Primary structure and functional expression of a rat G-protein-coupled muscarinic potassium channel., Kubo Y., Nature. August 26, 1993; 364 (6440): 802-6.

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