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Summary Anatomy Item Literature (3729) Expression Attributions Wiki
XB-ANAT-99

Papers associated with cardiovascular system (and kcnk3)

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Cloning, functional characterization, and remodeling of K2P3.1 (TASK-1) potassium channels in a porcine model of atrial fibrillation and heart failure., Schmidt C., Heart Rhythm. October 1, 2014; 11 (10): 1798-805.

Gain-of-function mutation in TASK-4 channels and severe cardiac conduction disorder., Friedrich C., EMBO Mol Med. July 1, 2014; 6 (7): 937-51.              

Class I antiarrhythmic drugs inhibit human cardiac two-pore-domain K(+) (K2 ₂p) channels., Schmidt C., Eur J Pharmacol. December 5, 2013; 721 (1-3): 237-48.

TASK1 (K(2P)3.1) K(+) channel inhibition by endothelin-1 is mediated through Rho kinase-dependent phosphorylation., Seyler C., Br J Pharmacol. March 1, 2012; 165 (5): 1467-75.

Carvedilol targets human K2P 3.1 (TASK1) K+ leak channels., Staudacher K., Br J Pharmacol. July 1, 2011; 163 (5): 1099-110.

TASK-1 channels may modulate action potential duration of human atrial cardiomyocytes., Limberg SH., Cell Physiol Biochem. January 1, 2011; 28 (4): 613-24.

The human cardiac K2P3.1 (TASK-1) potassium leak channel is a molecular target for the class III antiarrhythmic drug amiodarone., Gierten J., Naunyn Schmiedebergs Arch Pharmacol. March 1, 2010; 381 (3): 261-70.

Mycophenolic acid (MPA) and its glucuronide metabolites interact with transport systems responsible for excretion of organic anions in the basolateral membrane of the human kidney., Wolff NA., Nephrol Dial Transplant. September 1, 2007; 22 (9): 2497-503.

The acid-sensitive potassium channel TASK-1 in rat cardiac muscle., Putzke C., Cardiovasc Res. July 1, 2007; 75 (1): 59-68.

Inhibition of TASK-1 potassium channel by phospholipase C., Czirják G., Am J Physiol Cell Physiol. August 1, 2001; 281 (2): C700-8.

Block of Kcnk3 by protons. Evidence that 2-P-domain potassium channel subunits function as homodimers., Lopes CM., J Biol Chem. July 6, 2001; 276 (27): 24449-52.

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