Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

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

Papers associated with kcnj3



???displayGene.coCitedPapers???

???pagination.result.count???

???pagination.result.page??? ???pagination.result.prev??? 1 2 3 4 5 6 7 ???pagination.result.next???

Sort Newest To Oldest Sort Oldest To Newest

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


Molecular determinants for activation of G-protein-coupled inward rectifier K+ (GIRK) channels by extracellular acidosis., Mao J, Li L, McManus M, Wu J, Cui N, Jiang C., J Biol Chem. November 29, 2002; 277 (48): 46166-71.


G protein-coupled receptors form stable complexes with inwardly rectifying potassium channels and adenylyl cyclase., Lavine N, Ethier N, Oak JN, Pei L, Liu F, Trieu P, Rebois RV, Bouvier M, Hebert TE, Van Tol HH., J Biol Chem. November 29, 2002; 277 (48): 46010-9.


Distinct sites on G protein beta gamma subunits regulate different effector functions., Mirshahi T, Mittal V, Zhang H, Linder ME, Logothetis DE., J Biol Chem. September 27, 2002; 277 (39): 36345-50.


Graded contribution of the Gbeta gamma binding domains to GIRK channel activation., Sadja R, Alagem N, Reuveny E., Proc Natl Acad Sci U S A. August 6, 2002; 99 (16): 10783-8.


LB50053: a 5-hydroxytrypamine(1a) agent with a high binding affinity and a potency evoking a K(+) current., Kim HS, Cho T, Lee C, Lee C, Joo H, Kim S, Min CK., Pharmacology. August 1, 2002; 65 (4): 175-81.


Activator of G-protein signaling 1 blocks GIRK channel activation by a G-protein-coupled receptor: apparent disruption of receptor signaling complexes., Takesono A, Nowak MW, Cismowski M, Duzic E, Lanier SM., J Biol Chem. April 19, 2002; 277 (16): 13827-30.


Functional expression of a novel ginsenoside Rf binding protein from rat brain mRNA in Xenopus laevis oocytes., Choi S, Jung SY, Ko YS, Koh SR, Rhim H, Nah SY., Mol Pharmacol. April 1, 2002; 61 (4): 928-35.


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.


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.


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.


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.


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.


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.


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.


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.


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.


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.


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.


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.


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.


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.


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.


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.


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.


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.


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.


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.


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


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.


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.


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.


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.


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.              


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.


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.


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.


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.


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.


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.


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.

???pagination.result.page??? ???pagination.result.prev??? 1 2 3 4 5 6 7 ???pagination.result.next???