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Summary Anatomy Item Literature (12667) Expression Attributions Wiki
XB-ANAT-175

Papers associated with nervous system (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.


A revised mechanism of action of hyperaldosteronism-linked mutations in cytosolic domains of GIRK4 (KCNJ5)., Shalomov B., J Physiol. March 1, 2022; 600 (6): 1419-1437.


AsKC11, a Kunitz Peptide from Anemonia sulcata, Is a Novel Activator of G Protein-Coupled Inward-Rectifier Potassium Channels., An D., Mar Drugs. February 15, 2022; 20 (2):


A novel ion conducting route besides the central pore in an inherited mutant of G-protein-gated inwardly rectifying K+ channel., Chen IS., J Physiol. February 1, 2022; 600 (3): 603-622.


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):               


The small molecule GAT1508 activates brain-specific GIRK1/2 channel heteromers and facilitates conditioned fear extinction in rodents., Xu Y., J Biol Chem. March 13, 2020; 295 (11): 3614-3634.  


Cholesterol up-regulates neuronal G protein-gated inwardly rectifying potassium (GIRK) channel activity in the hippocampus., Bukiya AN., J Biol Chem. April 14, 2017; 292 (15): 6135-6147.


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.                  


Baclofen and other GABAB receptor agents are allosteric modulators of the CXCL12 chemokine receptor CXCR4., Guyon A., J Neurosci. July 10, 2013; 33 (28): 11643-54.


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.                


Voltage sensitivities and deactivation kinetics of histamine H₃ and H₄ receptors., Sahlholm K., Biochim Biophys Acta. December 1, 2012; 1818 (12): 3081-9.


Inhibition of g protein-activated inwardly rectifying k channels by phencyclidine., Kobayashi T., Curr Neuropharmacol. March 1, 2011; 9 (1): 244-6.    


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.            


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.


Further characterization of regulation of Ca(V)2.2 by stargazin., Tselnicker I., Channels (Austin). January 1, 2010; 4 (5): 351-4.


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.


The human histamine H3 receptor couples to GIRK channels in Xenopus oocytes., Sahlholm K., Eur J Pharmacol. July 19, 2007; 567 (3): 206-10.


Galphai3 primes the G protein-activated K+ channels for activation by coexpressed Gbetagamma in intact Xenopus oocytes., Rubinstein M., J Physiol. May 15, 2007; 581 (Pt 1): 17-32.


Inhibitory effect of gabapentin on N-methyl-D-aspartate receptors expressed in Xenopus oocytes., Hara K., Acta Anaesthesiol Scand. January 1, 2007; 51 (1): 122-8.


The GIRK1 brain variant GIRK1d and its functional impact on heteromultimeric GIRK channels., Steinecker B., J Recept Signal Transduct Res. January 1, 2007; 27 (5-6): 369-82.


RGS3 and RGS4 differentially associate with G protein-coupled receptor-Kir3 channel signaling complexes revealing two modes of RGS modulation. Precoupling and collision coupling., Jaén C., J Biol Chem. November 10, 2006; 281 (45): 34549-60.


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.


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.


Mutation of critical GIRK subunit residues disrupts N- and C-termini association and channel function., Sarac R., J Neurosci. February 16, 2005; 25 (7): 1836-46.


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.


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.


Inhibition of G protein-activated inwardly rectifying K+ channels by various antidepressant drugs., Kobayashi T., Neuropsychopharmacology. October 1, 2004; 29 (10): 1841-51.


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.


RGS9 modulates dopamine signaling in the basal ganglia., Rahman Z., Neuron. June 19, 2003; 38 (6): 941-52.


Inhibition of G protein-activated inwardly rectifying K+ channels by fluoxetine (Prozac)., Kobayashi T., Br J Pharmacol. March 1, 2003; 138 (6): 1119-28.


Single channel analysis of the regulation of GIRK1/GIRK4 channels by protein phosphorylation., Müllner D., Biophys J. February 1, 2003; 84 (2 Pt 1): 1399-409.


Early embryonic expression of ion channels and pumps in chick and Xenopus development., Rutenberg J., Dev Dyn. December 1, 2002; 225 (4): 469-84.                            


LB50053: a 5-hydroxytrypamine(1a) agent with a high binding affinity and a potency evoking a K(+) current., Kim HS., Pharmacology. August 1, 2002; 65 (4): 175-81.


Functional expression of a novel ginsenoside Rf binding protein from rat brain mRNA in Xenopus laevis oocytes., Choi S., Mol Pharmacol. April 1, 2002; 61 (4): 928-35.


Does acetaldehyde mediate ethanol action in the central nervous system?, Mascia MP., Alcohol Clin Exp Res. November 1, 2001; 25 (11): 1570-5.


Mechanism underlying bupivacaine inhibition of G protein-gated inwardly rectifying K+ channels., Zhou W., Proc Natl Acad Sci U S A. May 22, 2001; 98 (11): 6482-7.


Yeast screen for constitutively active mutant G protein-activated potassium channels., Yi BA., Neuron. March 1, 2001; 29 (3): 657-67.


Cloning and characterization of G protein-gated inward rectifier K+ channel (GIRK1) isoforms from heart and brain., Zhu L., J Mol Neurosci. February 1, 2001; 16 (1): 21-32.


G-protein mediated gating of inward-rectifier K+ channels., Mark MD., Eur J Biochem. October 1, 2000; 267 (19): 5830-6.


TrkB activation by brain-derived neurotrophic factor inhibits the G protein-gated inward rectifier Kir3 by tyrosine phosphorylation of the channel., Rogalski SL., J Biol Chem. August 18, 2000; 275 (33): 25082-8.


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.


Kir3.1/3.2 encodes an I(KACh)-like current in gastrointestinal myocytes., Bradley KK., Am J Physiol Gastrointest Liver Physiol. February 1, 2000; 278 (2): G289-96.


Ethanol opens G-protein-activated inwardly rectifying K+ channels., Kobayashi T., Nat Neurosci. December 1, 1999; 2 (12): 1091-7.


G-protein-coupled inwardly rectifying potassium channels are targets of alcohol action., Lewohl JM., Nat Neurosci. December 1, 1999; 2 (12): 1084-90.


Calcium sensing properties of the GABA(B) receptor., Wise A., Neuropharmacology. November 1, 1999; 38 (11): 1647-56.

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