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Bioelectric signaling: Reprogrammable circuits underlying embryogenesis, regeneration, and cancer. , Levin M ., Cell. April 15, 2021;
Bioelectric signalling via potassium channels: a mechanism for craniofacial dysmorphogenesis in KCNJ2-associated Andersen-Tawil Syndrome. , Adams DS ., J Physiol. June 15, 2016; 594 (12): 3245-70.
SPAK and OSR1 Sensitive Kir2.1 K+ Channels. , Fezai M., Neurosignals. January 1, 2015; 23 (1): 20-33.
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.
Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotype. , Ambrosini E., Hum Mol Genet. September 15, 2014; 23 (18): 4875-86.
A Kir3.4 mutation causes Andersen-Tawil syndrome by an inhibitory effect on Kir2.1. , Kokunai Y., Neurology. March 25, 2014; 82 (12): 1058-64.
Lack of negatively charged residues at the external mouth of Kir2.2 channels enable the voltage-dependent block by external Mg2+. , Li J., PLoS One. January 1, 2014; 9 (10): e111372.
Voltage-dependent inhibition of outward Kir2.1 currents by extracellular spermine. , Chang HK., Biochim Biophys Acta. February 1, 2013; 1828 (2): 765-75.
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 Kir2.1 ( KCNJ2) by the AMP-activated protein kinase. , Alesutan I., Biochem Biophys Res Commun. May 20, 2011; 408 (4): 505-10.
Inhibition of G protein-activated inwardly rectifying K+ channels by different classes of antidepressants. , Kobayashi T., PLoS One. January 1, 2011; 6 (12): e28208.
Differential effects of volatile and intravenous anesthetics on the activity of human TASK-1. , Putzke C., Am J Physiol Cell Physiol. October 1, 2007; 293 (4): C1319-26.
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.
Kir2.3 isoform confers pH sensitivity to heteromeric Kir2.1/ Kir2.3 channels in HEK293 cells. , Muñoz V., Heart Rhythm. April 1, 2007; 4 (4): 487-96.
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.
Polymorphic ventricular tachycardia and KCNJ2 mutations. , Chun TU., Heart Rhythm. July 1, 2004; 1 (2): 235-41.
Lefty blocks a subset of TGFbeta signals by antagonizing EGF- CFC coreceptors. , Cheng SK., PLoS Biol. February 1, 2004; 2 (2): E30.
Inhibition of G protein-activated inwardly rectifying K+ channels by fluoxetine (Prozac). , Kobayashi T., Br J Pharmacol. March 1, 2003; 138 (6): 1119-28.
Conformational changes in Kir2.1 channels during NH4+-induced inactivation. , Chang HK., J Biol Chem. January 10, 2003; 278 (2): 908-18.
Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome). , Tristani-Firouzi M., J Clin Invest. August 1, 2002; 110 (3): 381-8.
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.
Unitary conductance variation in Kir2.1 and in cardiac inward rectifier potassium channels. , Picones A., Biophys J. October 1, 2001; 81 (4): 2035-49.
Ammonium ions induce inactivation of Kir2.1 potassium channels expressed in Xenopus oocytes. , Shieh RC., J Physiol. September 1, 2001; 535 (Pt 2): 359-70.
Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome. , Plaster NM., Cell. May 18, 2001; 105 (4): 511-9.
Block of inwardly rectifying K+ currents by extracellular Mg2+ and Ba2+ in bovine pulmonary artery endothelial cells. , Leung YM., Can J Physiol Pharmacol. September 1, 2000; 78 (9): 751-6.
Expression cloning of KCRF, a potassium channel regulatory factor. , Keren-Raifman T., Biochem Biophys Res Commun. August 11, 2000; 274 (3): 852-8.
Mechanisms for the time-dependent decay of inward currents through cloned Kir2.1 channels expressed in Xenopus oocytes. , Shieh RC., J Physiol. July 15, 2000; 526 Pt 2 241-52.
Direct block of inward rectifier potassium channels by nicotine. , Wang H., Toxicol Appl Pharmacol. April 1, 2000; 164 (1): 97-101.
K+ binding sites and interactions between permeating K+ ions at the external pore mouth of an inward rectifier K+ channel ( Kir2.1). , Shieh RC., J Biol Chem. June 18, 1999; 274 (25): 17424-30.
The role of Kir2.1 in the genesis of native cardiac inward-rectifier K+ currents during pre- and postnatal development. , Nakamura TY., Ann N Y Acad Sci. April 30, 1999; 868 434-7.
Structural determinants of gating in inward-rectifier K+ channels. , Choe H., Biophys J. April 1, 1999; 76 (4): 1988-2003.
Kir2.1 encodes the inward rectifier potassium channel in rat arterial smooth muscle cells. , Bradley KK., J Physiol. March 15, 1999; 515 ( Pt 3) 639-51.
Molecular characterization of an inwardly rectifying K+ channel from HeLa cells. , Klein H., J Membr Biol. January 1, 1999; 167 (1): 43-52.
A novel crystallization method for visualizing the membrane localization of potassium channels. , Lopatin AN., Biophys J. May 1, 1998; 74 (5): 2159-70.
Inhibition of rat ventricular IK1 with antisense oligonucleotides targeted to Kir2.1 mRNA. , Nakamura TY., Am J Physiol. March 1, 1998; 274 (3): H892-900.
Specific block of cloned Herg channels by clofilium and its tertiary analog LY97241. , Suessbrich H., FEBS Lett. September 8, 1997; 414 (2): 435-8.
Molecular cloning and expression of a bovine endothelial inward rectifier potassium channel. , Forsyth SE., FEBS Lett. June 9, 1997; 409 (2): 277-82.
Molecular and functional heterogeneity of inward rectifier potassium channels in brain and heart. , Kurachi Y., J Card Fail. December 1, 1996; 2 (4 Suppl): S59-62.
Inward rectification of the IRK1 channel expressed in Xenopus oocytes: effects of intracellular pH reveal an intrinsic gating mechanism. , Shieh RC., J Physiol. July 15, 1996; 494 ( Pt 2) 363-76.
Susceptibility of cloned K+ channels to reactive oxygen species. , Duprat F., Proc Natl Acad Sci U S A. December 5, 1995; 92 (25): 11796-800.
Functional expression of a vertebrate inwardly rectifying K+ channel in yeast. , Tang W., Mol Biol Cell. September 1, 1995; 6 (9): 1231-40.
Cloning and functional characterization of a novel ATP-sensitive potassium channel ubiquitously expressed in rat tissues, including pancreatic islets, pituitary, skeletal muscle, and heart. , Inagaki N., J Biol Chem. March 17, 1995; 270 (11): 5691-4.
Cloning and functional expression of an inwardly rectifying K+ channel from human atrium. , Wible BA., Circ Res. March 1, 1995; 76 (3): 343-50.
Cloning, localization, and functional expression of a human brain inward rectifier potassium channel (hIRK1). , Tang W., Recept Channels. January 1, 1995; 3 (3): 175-83.
Molecular cloning and expression of a human heart inward rectifier potassium channel. , Raab-Graham KF., Neuroreport. December 20, 1994; 5 (18): 2501-5.
Gating mechanism of the cloned inward rectifier potassium channel from mouse heart. , Ishihara K., J Membr Biol. October 1, 1994; 142 (1): 55-64.
Molecular cloning and functional expression of cDNA encoding a second class of inward rectifier potassium channels in the mouse brain. , Takahashi N., J Biol Chem. September 16, 1994; 269 (37): 23274-9.
A region of the muscarinic-gated atrial K+ channel critical for activation by G protein beta gamma subunits. , Takao K., Neuron. September 1, 1994; 13 (3): 747-55.
Cloning and expression of a novel human brain inward rectifier potassium channel. , Makhina EN., J Biol Chem. August 12, 1994; 269 (32): 20468-74.
Cloning a novel human brain inward rectifier potassium channel and its functional expression in Xenopus oocytes. , Tang W., FEBS Lett. July 18, 1994; 348 (3): 239-43.