Papers associated with heart (and abcc8)

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	Kir6.2 activation by sulfonylurea receptors: a different mechanism of action for SUR1 and SUR2A subunits via the same residues., Principalli MA., Physiol Rep. September 1, 2015; 3 (9):
	Neurally Derived Tissues in Xenopus laevis Embryos Exhibit a Consistent Bioelectrical Left-Right Asymmetry., Pai VP., Stem Cells Int. January 1, 2012; 2012 353491.
	The ATP-sensitive K(+)-channel (K(ATP)) controls early left-right patterning in Xenopus and chick embryos., Aw S., Dev Biol. October 1, 2010; 346 (1): 39-53.
	Uncoupling by (--)-epigallocatechin-3-gallate of ATP-sensitive potassium channels from phosphatidylinositol polyphosphates and ATP., Jin JY., Pharmacol Res. September 1, 2007; 56 (3): 237-47.
	Functional effects of naturally occurring KCNJ11 mutations causing neonatal diabetes on cloned cardiac KATP channels., Tammaro P., J Physiol. February 15, 2006; 571 (Pt 1): 3-14.
	Differential selectivity of insulin secretagogues: mechanisms, clinical implications, and drug interactions., Gribble FM., J Diabetes Complications. January 1, 2003; 17 (2 Suppl): 11-5.
	Amiloride derivatives are potent blockers of KATP channels., Bollensdorff C., Naunyn Schmiedebergs Arch Pharmacol. October 1, 2001; 364 (4): 351-8.
	Structural basis for the interference between nicorandil and sulfonylurea action., Reimann F., Diabetes. October 1, 2001; 50 (10): 2253-9.
	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.
	Glimepiride block of cloned beta-cell, cardiac and smooth muscle K(ATP) channels., Song DK., Br J Pharmacol. May 1, 2001; 133 (1): 193-9.
	Effects of mitiglinide (S 21403) on Kir6.2/SUR1, Kir6.2/SUR2A and Kir6.2/SUR2B types of ATP-sensitive potassium channel., Reimann F., Br J Pharmacol. April 1, 2001; 132 (7): 1542-8.
	Nucleotide modulation of pinacidil stimulation of the cloned K(ATP) channel Kir6.2/SUR2A., Gribble FM., Mol Pharmacol. June 1, 2000; 57 (6): 1256-61.
	Rat homolog of sulfonylurea receptor 2B determines glibenclamide sensitivity of ROMK2 in Xenopus laevis oocyte., Tanemoto M., Am J Physiol Renal Physiol. April 1, 2000; 278 (4): F659-66.
	Altered functional properties of KATP channel conferred by a novel splice variant of SUR1., Sakura H., J Physiol. December 1, 1999; 521 Pt 2 337-50.
	Pharmacological plasticity of cardiac ATP-sensitive potassium channels toward diazoxide revealed by ADP., D'hahan N., Proc Natl Acad Sci U S A. October 12, 1999; 96 (21): 12162-7.
	A transmembrane domain of the sulfonylurea receptor mediates activation of ATP-sensitive K(+) channels by K(+) channel openers., D'hahan N., Mol Pharmacol. August 1, 1999; 56 (2): 308-15.
	Differential sensitivity of beta-cell and extrapancreatic K(ATP) channels to gliclazide., Gribble FM., Diabetologia. July 1, 1999; 42 (7): 845-8.
	Identification of the high-affinity tolbutamide site on the SUR1 subunit of the K(ATP) channel., Ashfield R., Diabetes. June 1, 1999; 48 (6): 1341-7.
	Tissue specificity of sulfonylureas: studies on cloned cardiac and beta-cell K(ATP) channels., Gribble FM., Diabetes. September 1, 1998; 47 (9): 1412-8.
	Phentolamine block of KATP channels is mediated by Kir6.2., Proks P., Proc Natl Acad Sci U S A. October 14, 1997; 94 (21): 11716-20.

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