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