Papers associated with embryonic structure (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.
	Diuresis by intravenous administration of xanthurenic acid in rats, and inhibition by probenecid., Uwai Y., Biomed Res. January 1, 2014; 35 (3): 223-6.
	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.
	Carvedilol targets human K2P 3.1 (TASK1) K+ leak channels., Staudacher K., Br J Pharmacol. July 1, 2011; 163 (5): 1099-110.
	Untargeted metabolomics identifies enterobiome metabolites and putative uremic toxins as substrates of organic anion transporter 1 (Oat1)., Wikoff WR., J Proteome Res. June 3, 2011; 10 (6): 2842-51.
	TASK-1 channels may modulate action potential duration of human atrial cardiomyocytes., Limberg SH., Cell Physiol Biochem. January 1, 2011; 28 (4): 613-24.
	Human sodium phosphate transporter 4 (hNPT4/SLC17A3) as a common renal secretory pathway for drugs and urate., Jutabha P., J Biol Chem. November 5, 2010; 285 (45): 35123-32.
	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.
	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.
	Developmentally regulated expression of organic ion transporters NKT (OAT1), OCT1, NLT (OAT2), and Roct., Pavlova A., Am J Physiol Renal Physiol. April 1, 2000; 278 (4): F635-43.
	Identification of multispecific organic anion transporter 2 expressed predominantly in the liver., Sekine T., FEBS Lett. June 12, 1998; 429 (2): 179-82.

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