Papers associated with oocyte (and kcnj2)

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	Identification of a unique endoplasmic retention motif in the Xenopus GIRK5 channel and its contribution to oocyte maturation., Rangel-Garcia CI., FEBS Open Bio. April 1, 2021; 11 (4): 1093-1108.
	Nocturnal Atrial Fibrillation Caused by Mutation in KCND2, Encoding Pore-Forming (α) Subunit of the Cardiac Kv4.2 Potassium Channel., Drabkin M., Circ Genom Precis Med. November 1, 2018; 11 (11): e002293.
	Dual Mechanism for Inhibition of Inwardly Rectifying Kir2.x Channels by Quinidine Involving Direct Pore Block and PIP2-interference., Koepple C., J Pharmacol Exp Ther. May 1, 2017; 361 (2): 209-218.
	Class III antiarrhythmic drug dronedarone inhibits cardiac inwardly rectifying Kir2.1 channels through binding at residue E224., Xynogalos P., Naunyn Schmiedebergs Arch Pharmacol. December 1, 2014; 387 (12): 1153-61.
	Conformational changes underlying pore dilation in the cytoplasmic domain of mammalian inward rectifier K+ channels., Inanobe A., PLoS One. January 1, 2013; 8 (11): e79844.
	Inhibition of cardiac Kir2.1-2.3 channels by beta3 adrenoreceptor antagonist SR 59230A., Kulzer M., Biochem Biophys Res Commun. July 27, 2012; 424 (2): 315-20.
	Discovery, characterization, and structure-activity relationships of an inhibitor of inward rectifier potassium (Kir) channels with preference for Kir2.3, Kir3.x, and Kir7.1., Raphemot R., Front Pharmacol. November 30, 2011; 2 75.
	Inhibition of g protein-activated inwardly rectifying k channels by phencyclidine., Kobayashi T., Curr Neuropharmacol. March 1, 2011; 9 (1): 244-6.
	Inhibition of G protein-activated inwardly rectifying K+ channels by different classes of antidepressants., Kobayashi T., PLoS One. January 1, 2011; 6 (12): e28208.
	Pregnenolone sulfate potentiates the inwardly rectifying K channel Kir2.3., Kobayashi T., PLoS One. July 21, 2009; 4 (7): e6311.
	Structural changes in the cytoplasmic pore of the Kir1.1 channel during pHi-gating probed by FRET., Lee JR., J Biomed Sci. March 6, 2009; 16 29.
	Inhibition by cocaine of G protein-activated inwardly rectifying K+ channels expressed in Xenopus oocytes., Kobayashi T., Toxicol In Vitro. June 1, 2007; 21 (4): 656-64.
	Selective inhibition of Kir currents by antihistamines., Liu B., Eur J Pharmacol. March 8, 2007; 558 (1-3): 21-6.
	Functional and clinical characterization of a mutation in KCNJ2 associated with Andersen-Tawil syndrome., Lu CW., J Med Genet. August 1, 2006; 43 (8): 653-9.
	Andersen-Tawil syndrome: new potassium channel mutations and possible phenotypic variation., Davies NP., Neurology. October 11, 2005; 65 (7): 1083-9.
	Carboxy-terminal determinants of conductance in inward-rectifier K channels., Zhang YY., J Gen Physiol. December 1, 2004; 124 (6): 729-39.
	Regulation of Kir channels by intracellular pH and extracellular K(+): mechanisms of coupling., Dahlmann A., J Gen Physiol. April 1, 2004; 123 (4): 441-54.
	Mechanism of rectification in inward-rectifier K+ channels., Guo D., J Gen Physiol. April 1, 2003; 121 (4): 261-75.
	Inhibition of G protein-activated inwardly rectifying K+ channels by fluoxetine (Prozac)., Kobayashi T., Br J Pharmacol. March 1, 2003; 138 (6): 1119-28.
	Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia., Ai T., Circulation. June 4, 2002; 105 (22): 2592-4.
	Permeant ion-dependent changes in gating of Kir2.1 inward rectifier potassium channels., Lu T., J Gen Physiol. November 1, 2001; 118 (5): 509-22.
	Mutations within the P-loop of Kir6.2 modulate the intraburst kinetics of the ATP-sensitive potassium channel., Proks P., J Gen Physiol. October 1, 2001; 118 (4): 341-53.
	Tyrosine decaging leads to substantial membrane trafficking during modulation of an inward rectifier potassium channel., Tong Y., J Gen Physiol. February 1, 2001; 117 (2): 103-18.
	Nonindependent K+ movement through the pore in IRK1 potassium channels., Stampe P., J Gen Physiol. October 1, 1998; 112 (4): 475-84.
	Properties of cloned ATP-sensitive K+ currents expressed in Xenopus oocytes., Gribble FM., J Physiol. January 1, 1997; 498 ( Pt 1) 87-98.
	Inward rectification of the IRK1 K+ channel reconstituted in lipid bilayers., Aleksandrov A., Biophys J. June 1, 1996; 70 (6): 2680-7.
	Dominant negative chimeras provide evidence for homo and heteromultimeric assembly of inward rectifier K+ channel proteins via their N-terminal end., Fink M., FEBS Lett. January 2, 1996; 378 (1): 64-8.

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