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Functional Characterization of a Spectrum of Novel Romano-Ward Syndrome KCNQ1 Variants. , Rinné S., Int J Mol Sci. January 10, 2023; 24 (2):
Eag Domains Regulate LQT Mutant hERG Channels in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes. , Liu QN., PLoS One. April 22, 2015; 10 (4): e0123951.
Functional assembly of Kv7.1/ Kv7.5 channels with emerging properties on vascular muscle physiology. , Oliveras A., Arterioscler Thromb Vasc Biol. July 1, 2014; 34 (7): 1522-30.
18β-Glycyrrhetinic acid preferentially blocks late Na current generated by ΔKPQ Nav1.5 channels. , Du YM., Acta Pharmacol Sin. June 1, 2012; 33 (6): 752-60.
Extracellular potassium inhibits Kv7.1 potassium channels by stabilizing an inactivated state. , Larsen AP., Biophys J. August 17, 2011; 101 (4): 818-27.
PKC activation and PIP(2) depletion underlie biphasic regulation of IKs by Gq-coupled receptors. , Matavel A., J Mol Cell Cardiol. May 1, 2009; 46 (5): 704-12.
Chlorthalidone inhibits the KvLQT1 potassium current in guinea-pig ventricular myocytes and oocytes from Xenopus laevis. , Mancilla-Simbro C., Br J Pharmacol. February 1, 2008; 153 (3): 448-58.
Human beta(3)-adrenoreceptors couple to KvLQT1/ MinK potassium channels in Xenopus oocytes via protein kinase C phosphorylation of the KvLQT1 protein. , Kathöfer S., Naunyn Schmiedebergs Arch Pharmacol. August 1, 2003; 368 (2): 119-26.
Interaction with GM130 during HERG ion channel trafficking. Disruption by type 2 congenital long QT syndrome mutations. Human Ether-à- go-go-Related Gene. , Roti EC., J Biol Chem. December 6, 2002; 277 (49): 47779-85.
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.
Chromanol 293B, a blocker of the slow delayed rectifier K+ current (IKs), inhibits the CFTR Cl- current. , Bachmann A., Naunyn Schmiedebergs Arch Pharmacol. June 1, 2001; 363 (6): 590-6.
Short- and long-term effects of amiodarone on the two components of cardiac delayed rectifier K(+) current. , Kamiya K., Circulation. March 6, 2001; 103 (9): 1317-24.
Functional coupling of human beta 3-adrenoreceptors to the KvLQT1/ MinK potassium channel. , Kathöfer S., J Biol Chem. September 1, 2000; 275 (35): 26743-7.
KChAP as a chaperone for specific K(+) channels. , Kuryshev YA., Am J Physiol Cell Physiol. May 1, 2000; 278 (5): C931-41.
Single-channel characteristics of wild-type IKs channels and channels formed with two minK mutants that cause long QT syndrome. , Sesti F., J Gen Physiol. December 1, 1998; 112 (6): 651-63.
Independent and exclusive modulation of cardiac delayed rectifying K+ current by protein kinase C and protein kinase A. , Lo CF., Circ Res. November 16, 1998; 83 (10): 995-1002.
A novel benzodiazepine that activates cardiac slow delayed rectifier K+ currents. , Salata JJ., Mol Pharmacol. July 1, 1998; 54 (1): 220-30.
Suppression of slow delayed rectifier current by a truncated isoform of KvLQT1 cloned from normal human heart. , Jiang M., J Biol Chem. September 26, 1997; 272 (39): 24109-12.
A minK- HERG complex regulates the cardiac potassium current I(Kr). , McDonald TV., Nature. July 17, 1997; 388 (6639): 289-92.
Coassembly of K(V)LQT1 and minK ( IsK) proteins to form cardiac I(Ks) potassium channel. , Sanguinetti MC., Nature. November 7, 1996; 384 (6604): 80-3.
A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel. , Sanguinetti MC., Cell. April 21, 1995; 81 (2): 299-307.