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Summary Expression Phenotypes Gene Literature (308) GO Terms (6) Nucleotides (92) Proteins (53) Interactants (177) Wiki
XB-GENEPAGE-1004370

Papers associated with kcnj3



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Mechanisms of inward-rectifier K+ channel inhibition by tertiapin-Q., Jin W, Klem AM, Lewis JH, Lu Z., Biochemistry. October 26, 1999; 38 (43): 14294-301.

Synthesis of a stable form of tertiapin: a high-affinity inhibitor for inward-rectifier K+ channels., Jin W, Lu Z., Biochemistry. October 26, 1999; 38 (43): 14286-93.

Calcium sensing properties of the GABA(B) receptor., Wise A, Green A, Main MJ, Wilson R, Fraser N, Marshall FH., Neuropharmacology. November 1, 1999; 38 (11): 1647-56.

Molecular mechanism for sodium-dependent activation of G protein-gated K+ channels., Ho IH, Murrell-Lagnado RD., J Physiol. November 1, 1999; 520 Pt 3 645-51.

Reverse physiology in drosophila: identification of a novel allatostatin-like neuropeptide and its cognate receptor structurally related to the mammalian somatostatin/galanin/opioid receptor family., Birgül N, Weise C, Kreienkamp HJ, Richter D., EMBO J. November 1, 1999; 18 (21): 5892-900.

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, Sui JL, Logothetis DE., 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, Griffin G, Satin LS, Abood ME., J Pharmacol Exp Ther. November 1, 1999; 291 (2): 618-26.

Molecular cloning and characterization of a novel splicing variant of the Kir3.2 subunit predominantly expressed in mouse testis., Inanobe A, Horio Y, Fujita A, Tanemoto M, Hibino H, Inageda K, Kurachi Y., J Physiol. November 15, 1999; 521 Pt 1 19-30.

Ethanol opens G-protein-activated inwardly rectifying K+ channels., Kobayashi T, Ikeda K, Kojima H, Niki H, Yano R, Yoshioka T, Kumanishi T., Nat Neurosci. December 1, 1999; 2 (12): 1091-7.

G-protein-coupled inwardly rectifying potassium channels are targets of alcohol action., Lewohl JM, Wilson WR, Mayfield RD, Brozowski SJ, Morrisett RA, Harris RA., Nat Neurosci. December 1, 1999; 2 (12): 1084-90.

The dual modulation of GIRK1/GIRK2 channels by opioid receptor ligands., Ulens C, Daenens P, Tytgat J., Eur J Pharmacol. December 3, 1999; 385 (2-3): 239-45.

Distinct specificities of inwardly rectifying K(+) channels for phosphoinositides., Rohács T, Chen J, Prestwich GD, Logothetis DE., J Biol Chem. December 17, 1999; 274 (51): 36065-72.

Kir3.1/3.2 encodes an I(KACh)-like current in gastrointestinal myocytes., Bradley KK, Hatton WJ, Mason HS, Walker RL, Flynn ER, Kenyon JL, Horowitz B., Am J Physiol Gastrointest Liver Physiol. February 1, 2000; 278 (2): G289-96.

Co-expression of Gbeta5 enhances the function of two Ggamma subunit-like domain-containing regulators of G protein signaling proteins., Kovoor A, Chen CK, He W, Wensel TG, Simon MI, Lester HA., J Biol Chem. February 4, 2000; 275 (5): 3397-402.

Coupling of the muscarinic m2 receptor to G protein-activated K(+) channels via Galpha(z) and a receptor-Galpha(z) fusion protein. Fusion between the receptor and Galpha(z) eliminates catalytic (collision) coupling., Vorobiov D, Bera AK, Keren-Raifman T, Barzilai R, Dascal N., J Biol Chem. February 11, 2000; 275 (6): 4166-70.

Inhibition by various antipsychotic drugs of the G-protein-activated inwardly rectifying K(+) (GIRK) channels expressed in xenopus oocytes., Kobayashi T, Ikeda K, Kumanishi T., Br J Pharmacol. April 1, 2000; 129 (8): 1716-22.

Slow modal gating of single G protein-activated K+ channels expressed in Xenopus oocytes., Yakubovich D, Pastushenko V, Bitler A, Dessauer CW, Dascal N., 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, Vorobiov D, Bera AK, Uezono Y, Yakubovich D, Frohnwieser-Steinecker B, Dascal N, Schreibmayer W., J Gen Physiol. May 1, 2000; 115 (5): 547-58.              

Expression cloning of KCRF, a potassium channel regulatory factor., Keren-Raifman T, Ivanina T, Bismuth Y, Dascal N., Biochem Biophys Res Commun. August 11, 2000; 274 (3): 852-8.

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

Cs+ block of the cardiac muscarinic K+ channel, GIRK1/GIRK4, is not dependent on the aspartate residue at position 173., Dibb KM, Leach R, Lancaster MK, Findlay JB, Boyett MR., Pflugers Arch. September 1, 2000; 440 (5): 740-4.

Regulation of GIRK channel deactivation by Galpha(q) and Galpha(i/o) pathways., Mark MD, Ruppersberg JP, Herlitze S., Neuropharmacology. September 1, 2000; 39 (12): 2360-73.

Interaction of p-fluorofentanyl on cloned human opioid receptors and exploration of the role of Trp-318 and His-319 in mu-opioid receptor selectivity., Ulens C, Van Boven M, Daenens P, Tytgat J., J Pharmacol Exp Ther. September 1, 2000; 294 (3): 1024-33.

Changes in GIRK1/GIRK2 deactivation kinetics and basal activity in the presence and absence of RGS4., Ulens C, Daenens P, Tytgat J., Life Sci. September 29, 2000; 67 (19): 2305-17.

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

Genomic analysis and functional expression of canine dopamine D2 receptor., Myeong H, Jeoung D, Kim H, Ha JH, Lee Y, Kim KH, Park C, Kaang BK., Gene. October 17, 2000; 257 (1): 99-107.

Single channel studies of inward rectifier potassium channel regulation by muscarinic acetylcholine receptors., Bard J, Kunkel MT, Peralta EG., J Gen Physiol. November 1, 2000; 116 (5): 645-52.          

Characterization of GAR-2, a novel G protein-linked acetylcholine receptor from Caenorhabditis elegans., Lee YS, Park YS, Nam S, Suh SJ, Lee J, Lee J, Kaang BK, Cho NJ., J Neurochem. November 1, 2000; 75 (5): 1800-9.

Residues and mechanisms for slow activation and Ba2+ block of the cardiac muscarinic K+ channel, Kir3.1/Kir3.4., Lancaster MK, Dibb KM, Quinn CC, Leach R, Lee JK, Lee JK, Findlay JB, Boyett MR., J Biol Chem. November 17, 2000; 275 (46): 35831-9.

IK.ACh activation by arachidonic acid occurs via a G-protein-independent pathway mediated by the GIRK1 subunit., Lohberger B, Groschner K, Tritthart H, Schreibmayer W., Pflugers Arch. December 1, 2000; 441 (2-3): 251-6.

Kinetics of recovery from opioids at wild-type and mutant mu opioid receptors expressed in xenopus oocytes., Spivak CE, Beglan CL., Synapse. December 1, 2000; 38 (3): 254-60.

Cloning and characterization of G protein-gated inward rectifier K+ channel (GIRK1) isoforms from heart and brain., Zhu L, Wu X, Wu MB, Chan KW, Logothetis DE, Thornhill WB., J Mol Neurosci. February 1, 2001; 16 (1): 21-32.

Ion selectivity filter regulates local anesthetic inhibition of G-protein-gated inwardly rectifying K+ channels., Slesinger PA., Biophys J. February 1, 2001; 80 (2): 707-18.

Inhibition of a Gi-activated potassium channel (GIRK1/4) by the Gq-coupled m1 muscarinic acetylcholine receptor., Hill JJ, Peralta EG., J Biol Chem. February 23, 2001; 276 (8): 5505-10.

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

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, Bera AK, Zveig D, Peleg S, Witherow DS, Slepak VZ, Dascal N., FEBS Lett. March 9, 2001; 492 (1-2): 20-8.

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

Characterization of heteromultimeric G protein-coupled inwardly rectifying potassium channels of the tunicate tadpole with a unique pore property., Murata Y, Okado H, Kubo Y., J Biol Chem. May 25, 2001; 276 (21): 18529-39.

Differential effects of general anesthetics on G protein-coupled inwardly rectifying and other potassium channels., Yamakura T, Lewohl JM, Harris RA., Anesthesiology. July 1, 2001; 95 (1): 144-53.

Identification of G protein-coupled, inward rectifier potassium channel gene products from the rat anterior pituitary gland., Gregerson KA, Flagg TP, O'Neill TJ, Anderson M, Lauring O, Horel JS, Welling PA., Endocrinology. July 1, 2001; 142 (7): 2820-32.

G protein-gated inwardly rectifying potassium channels are targets for volatile anesthetics., Weigl LG, Schreibmayer W., Mol Pharmacol. August 1, 2001; 60 (2): 282-9.

Redox-dependent gating of G protein-coupled inwardly rectifying K+ channels., Zeidner G, Sadja R, Reuveny E., J Biol Chem. September 21, 2001; 276 (38): 35564-70.

The role of the hydrophilic Asn230 residue of the mu-opioid receptor in the potency of various opioid agonists., Pil J, Tytgat J., Br J Pharmacol. October 1, 2001; 134 (3): 496-506.

Does acetaldehyde mediate ethanol action in the central nervous system?, Mascia MP, Maiya R, Borghese CM, Lobo IA, Hara K, Yamakura T, Gong DH, Beckstead MJ., Alcohol Clin Exp Res. November 1, 2001; 25 (11): 1570-5.

Morphine-6beta-glucuronide and morphine-3-glucuronide, opioid receptor agonists with different potencies., Ulens C, Baker L, Ratka A, Waumans D, Tytgat J., Biochem Pharmacol. November 1, 2001; 62 (9): 1273-82.

Three functional isoforms of GAR-2, a Caenorhabditis elegans G-protein-linked acetylcholine receptor, are produced by alternative splicing., Suh SJ, Park YS, Lee YS, Cho TJ, Kaang BK, Cho NJ., Biochem Biophys Res Commun. November 16, 2001; 288 (5): 1238-43.

Ligand-induced signal transduction within heterodimeric GABA(B) receptor., Margeta-Mitrovic M, Jan YN, Jan LY., Proc Natl Acad Sci U S A. December 4, 2001; 98 (25): 14643-8.

Functional characterization of an endogenous Xenopus oocyte adenosine receptor., Kobayashi T, Ikeda K, Kumanishi T., Br J Pharmacol. January 1, 2002; 135 (2): 313-22.

G(alpha)(i) controls the gating of the G protein-activated K(+) channel, GIRK., Peleg S, Varon D, Ivanina T, Dessauer CW, Dascal N., Neuron. January 3, 2002; 33 (1): 87-99.

Gbeta residues that do not interact with Galpha underlie agonist-independent activity of K+ channels., Mirshahi T, Robillard L, Zhang H, Hébert TE, Logothetis DE., J Biol Chem. March 1, 2002; 277 (9): 7348-55.

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