Papers associated with endocrine cell (and abcc8)

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	A novel high-affinity inhibitor against the human ATP-sensitive Kir6.2 channel., Ramu Y., J Gen Physiol. July 2, 2018; 150 (7): 969-976.
	Binding of sulphonylureas to plasma proteins - A KATP channel perspective., Proks P., PLoS One. May 15, 2018; 13 (5): e0197634.
	Transient expression of Ngn3 in Xenopus endoderm promotes early and ectopic development of pancreatic beta and delta cells., Oropeza D., Genesis. March 1, 2012; 50 (3): 271-85.
	Disease progression and search for monogenic diabetes among children with new onset type 1 diabetes negative for ICA, GAD- and IA-2 Antibodies., Pörksen S., BMC Endocr Disord. September 23, 2010; 10 16.
	Functional analysis of two Kir6.2 (KCNJ11) mutations, K170T and E322K, causing neonatal diabetes., Tarasov AI., Diabetes Obes Metab. November 1, 2007; 9 Suppl 2 46-55.
	Iptakalim, a vascular ATP-sensitive potassium (KATP) channel opener, closes rat pancreatic beta-cell KATP channels and increases insulin release., Misaki N., J Pharmacol Exp Ther. August 1, 2007; 322 (2): 871-8.
	Scavenging of 14-3-3 proteins reveals their involvement in the cell-surface transport of ATP-sensitive K+ channels., Heusser K., J Cell Sci. October 15, 2006; 119 (Pt 20): 4353-63.
	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.
	Potent and selective activation of the pancreatic beta-cell type K(ATP) channel by two novel diazoxide analogues., Dabrowski M., Diabetologia. October 1, 2003; 46 (10): 1375-82.
	Analysis of the differential modulation of sulphonylurea block of beta-cell and cardiac ATP-sensitive K+ (K(ATP)) channels by Mg-nucleotides., Reimann F., J Physiol. February 15, 2003; 547 (Pt 1): 159-68.
	The novel diazoxide analog 3-isopropylamino-7-methoxy-4H-1,2,4-benzothiadiazine 1,1-dioxide is a selective Kir6.2/SUR1 channel opener., Dabrowski M., Diabetes. June 1, 2002; 51 (6): 1896-906.
	Structural basis for the interference between nicorandil and sulfonylurea action., Reimann F., Diabetes. October 1, 2001; 50 (10): 2253-9.
	The imidazoline RX871024 stimulates insulin secretion in pancreatic beta-cells from mice deficient in K(ATP) channel function., Efanov AM., Biochem Biophys Res Commun. June 22, 2001; 284 (4): 918-22.
	Effect of repaglinide on cloned beta cell, cardiac and smooth muscle types of ATP-sensitive potassium channels., Dabrowski M., Diabetologia. June 1, 2001; 44 (6): 747-56.
	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.
	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.
	Interaction of vanadate with the cloned beta cell K(ATP) channel., Proks P., J Biol Chem. September 3, 1999; 274 (36): 25393-7.
	Differential sensitivity of beta-cell and extrapancreatic K(ATP) channels to gliclazide., Gribble FM., Diabetologia. July 1, 1999; 42 (7): 845-8.
	KATP channel inhibition by ATP requires distinct functional domains of the cytoplasmic C terminus of the pore-forming subunit., Drain P., Proc Natl Acad Sci U S A. November 10, 1998; 95 (23): 13953-8.
	Mechanism of cloned ATP-sensitive potassium channel activation by oleoyl-CoA., Gribble FM., J Biol Chem. October 9, 1998; 273 (41): 26383-7.
	Tissue specificity of sulfonylureas: studies on cloned cardiac and beta-cell K(ATP) channels., Gribble FM., Diabetes. September 1, 1998; 47 (9): 1412-8.
	Molecular analysis of ATP-sensitive K channel gating and implications for channel inhibition by ATP., Trapp S., J Gen Physiol. September 1, 1998; 112 (3): 333-49.
	Mechanism of ATP-sensitive K channel inhibition by sulfhydryl modification., Trapp S., J Gen Physiol. September 1, 1998; 112 (3): 325-32.
	MgATP activates the beta cell KATP channel by interaction with its SUR1 subunit., Gribble FM., Proc Natl Acad Sci U S A. June 9, 1998; 95 (12): 7185-90.
	Inhibition of the ATP-sensitive potassium channel from mouse pancreatic beta-cells by surfactants., Smith PA., Br J Pharmacol. June 1, 1998; 124 (3): 529-39.
	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.
	The interaction of nucleotides with the tolbutamide block of cloned ATP-sensitive K+ channel currents expressed in Xenopus oocytes: a reinterpretation., Gribble FM., J Physiol. October 1, 1997; 504 ( Pt 1) 35-45.
	Activation and inhibition of K-ATP currents by guanine nucleotides is mediated by different channel subunits., Trapp S., Proc Natl Acad Sci U S A. August 5, 1997; 94 (16): 8872-7.
	Properties of cloned ATP-sensitive K+ currents expressed in Xenopus oocytes., Gribble FM., J Physiol. January 1, 1997; 498 ( Pt 1) 87-98.
	Sequence variations in the human Kir6.2 gene, a subunit of the beta-cell ATP-sensitive K-channel: no association with NIDDM in while Caucasian subjects or evidence of abnormal function when expressed in vitro., Sakura H., Diabetologia. October 1, 1996; 39 (10): 1233-6.

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