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Role of the C-terminus of SUR in the differential regulation of β-cell and cardiac KATP channels by MgADP and metabolism. , Vedovato N, Rorsman O, Hennis K, Ashcroft FM, Proks P., J Physiol. December 1, 2018; 596 (24): 6205-6217.
Sensitivity of KATP channels to cellular metabolic disorders and the underlying structural basis. , Li CG, Cui WY, Wang H., Acta Pharmacol Sin. January 1, 2016; 37 (1): 134-42.
Kir6.2 activation by sulfonylurea receptors: a different mechanism of action for SUR1 and SUR2A subunits via the same residues. , Principalli MA, Dupuis JP, Moreau CJ, Vivaudou M, Revilloud J., Physiol Rep. September 1, 2015; 3 (9):
Sulfonylureas suppress the stimulatory action of Mg-nucleotides on Kir6.2/ SUR1 but not Kir6.2/ SUR2A KATP channels: a mechanistic study. , Proks P, de Wet H, Ashcroft FM., J Gen Physiol. November 1, 2014; 144 (5): 469-86.
Essential role of the zinc finger transcription factor Casz1 for mammalian cardiac morphogenesis and development. , Liu Z, Li W , Ma X, Ding N, Spallotta F, Southon E, Tessarollo L, Gaetano C, Mukouyama YS, Thiele CJ., J Biol Chem. October 24, 2014; 289 (43): 29801-16.
The unusual stoichiometry of ADP activation of the KATP channel. , Hosy E, Vivaudou M., Front Physiol. January 28, 2014; 5 11.
Neurally Derived Tissues in Xenopus laevis Embryos Exhibit a Consistent Bioelectrical Left- Right Asymmetry. , Pai VP , Vandenberg LN, Blackiston D , Levin M ., 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, Koster JC, Pearson W, Nichols CG, Shi NQ, Carneiro K, Levin M ., Dev Biol. October 1, 2010; 346 (1): 39-53.
Targeting hypertension with a new adenosine triphosphate-sensitive potassium channel opener iptakalim. , Pan Z, Huang J, Cui W, Long C, Zhang Y , Wang H., J Cardiovasc Pharmacol. September 1, 2010; 56 (3): 215-28.
Impact of disease-causing SUR1 mutations on the KATP channel subunit interface probed with a rhodamine protection assay. , Hosy E, Dupuis JP, Vivaudou M., J Biol Chem. January 29, 2010; 285 (5): 3084-91.
Coassembly of different sulfonylurea receptor subtypes extends the phenotypic diversity of ATP-sensitive potassium (KATP) channels. , Wheeler A, Wang C , Yang K, Fang K, Davis K, Styer AM, Mirshahi U, Moreau C, Revilloud J, Vivaudou M, Liu S , Mirshahi T, Chan KW., Mol Pharmacol. November 1, 2008; 74 (5): 1333-44.
Three C-terminal residues from the sulphonylurea receptor contribute to the functional coupling between the K(ATP) channel subunits SUR2A and Kir6.2. , Dupuis JP, Revilloud J, Moreau CJ, Vivaudou M., J Physiol. July 1, 2008; 586 (13): 3075-85.
Sulfonylurea receptors type 1 and 2A randomly assemble to form heteromeric KATP channels of mixed subunit composition. , Chan KW, Wheeler A, Csanády L., J Gen Physiol. January 1, 2008; 131 (1): 43-58.
A mutation in the ATP-binding site of the Kir6.2 subunit of the KATP channel alters coupling with the SUR2A subunit. , Tammaro P, Ashcroft FM., J Physiol. November 1, 2007; 584 (Pt 3): 743-53.
The Kir6.2-F333I mutation differentially modulates KATP channels composed of SUR1 or SUR2 subunits. , Tammaro P, Ashcroft F., J Physiol. June 15, 2007; 581 (Pt 3): 1259-69.
Electrophysiological and pharmacological characterization of the K(ATP) channel involved in the K+-current responses to FSH and adenosine in the follicular cells of Xenopus oocyte. , Fujita R, Kimura S, Kawasaki S, Watanabe S, Watanabe N, Hirano H, Matsumoto M, Sasaki K., J Physiol Sci. February 1, 2007; 57 (1): 51-61.
The N-terminal transmembrane domain (TMD0) and a cytosolic linker (L0) of sulphonylurea receptor define the unique intrinsic gating of KATP channels. , Fang K, Csanády L, Chan KW., J Physiol. October 15, 2006; 576 (Pt 2): 379-89.
Functional effects of naturally occurring KCNJ11 mutations causing neonatal diabetes on cloned cardiac KATP channels. , Tammaro P, Proks P, Ashcroft FM., J Physiol. February 15, 2006; 571 (Pt 1): 3-14.
Effect of two amino acids in TM17 of Sulfonylurea receptor SUR1 on the binding of ATP-sensitive K+ channel modulators. , Hambrock A, Kayar T, Stumpp D, Osswald H., Diabetes. December 1, 2004; 53 Suppl 3 S128-34.
Taurine block of cloned ATP-sensitive K+ channels with different sulfonylurea receptor subunits expressed in Xenopus laevis oocytes. , Lim JG, Lee HY , Yun JE, Kim SP, Park JW , Suh SI, Jang BC, Cho CH, Bae JH, Kim SS, Han J , Park MJ, Song DK., Biochem Pharmacol. September 1, 2004; 68 (5): 901-10.
Zinc is both an intracellular and extracellular regulator of KATP channel function. , Prost AL, Bloc A, Hussy N, Derand R, Vivaudou M., J Physiol. August 15, 2004; 559 (Pt 1): 157-67.
Inhibition of ATP-sensitive K+ channels by substituted benzo[c]quinolizinium CFTR activators. , Prost A, Dérand R, Gros L, Becq F, Vivaudou M., Biochem Pharmacol. August 1, 2003; 66 (3): 425-30.
Analysis of the differential modulation of sulphonylurea block of beta-cell and cardiac ATP-sensitive K+ (K(ATP)) channels by Mg-nucleotides. , Reimann F, Dabrowski M, Jones P, Gribble FM, Ashcroft FM., J Physiol. February 15, 2003; 547 (Pt 1): 159-68.
Differential selectivity of insulin secretagogues: mechanisms, clinical implications, and drug interactions. , Gribble FM, Reimann F., J Diabetes Complications. January 1, 2003; 17 (2 Suppl): 11-5.
K(ATP) channel activity is required for hatching in Xenopus embryos. , Cheng SM, Chen I, Levin M ., Dev Dyn. December 1, 2002; 225 (4): 588-91.
Mutations in the linker domain of NBD2 of SUR inhibit transduction but not nucleotide binding. , Matsuo M, Dabrowski M, Ueda K, Ashcroft FM., EMBO J. August 15, 2002; 21 (16): 4250-8.
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, Ashcroft FM, Ashfield R, Lebrun P, Pirotte B, Egebjerg J, Bondo Hansen J, Wahl P., Diabetes. June 1, 2002; 51 (6): 1896-906.
Cloning of rabbit Kir6.1, SUR2A, and SUR2B: possible candidates for a renal K(ATP) channel. , Brochiero E, Wallendorf B, Gagnon D, Laprade R, Lapointe JY., Am J Physiol Renal Physiol. February 1, 2002; 282 (2): F289-300.
Amiloride derivatives are potent blockers of KATP channels. , Bollensdorff C, Zimmer T, Benndorf K., Naunyn Schmiedebergs Arch Pharmacol. October 1, 2001; 364 (4): 351-8.
Structural basis for the interference between nicorandil and sulfonylurea action. , Reimann F, Ashcroft FM, Gribble FM., Diabetes. October 1, 2001; 50 (10): 2253-9.
Effect of repaglinide on cloned beta cell, cardiac and smooth muscle types of ATP-sensitive potassium channels. , Dabrowski M, Wahl P, Holmes WE, Ashcroft FM., Diabetologia. June 1, 2001; 44 (6): 747-56.
Glimepiride block of cloned beta-cell, cardiac and smooth muscle K(ATP) channels. , Song DK, Ashcroft FM., Br J Pharmacol. May 1, 2001; 133 (1): 193-9.
Phospholipids as modulators of K(ATP) channels: distinct mechanisms for control of sensitivity to sulphonylureas, K(+) channel openers, and ATP. , Krauter T, Ruppersberg JP, Baukrowitz T., Mol Pharmacol. May 1, 2001; 59 (5): 1086-93.
Effects of mitiglinide (S 21403) on Kir6.2/ SUR1, Kir6.2/ SUR2A and Kir6.2/SUR2B types of ATP-sensitive potassium channel. , Reimann F, Proks P, Ashcroft FM., Br J Pharmacol. April 1, 2001; 132 (7): 1542-8.
Interaction of stilbene disulphonates with cloned K(ATP) channels. , Proks P, Jones P, Ashcroft FM., Br J Pharmacol. March 1, 2001; 132 (5): 973-82.
Differential response of K(ATP) channels containing SUR2A or SUR2B subunits to nucleotides and pinacidil. , Reimann F, Gribble FM, Ashcroft FM., Mol Pharmacol. December 1, 2000; 58 (6): 1318-25.
Nucleotide modulation of pinacidil stimulation of the cloned K(ATP) channel Kir6.2/ SUR2A. , Gribble FM, Reimann F, Ashfield R, Ashcroft 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, Vanoye CG, Dong K, Welch R, Abe T, Hebert SC, Xu JZ., Am J Physiol Renal Physiol. April 1, 2000; 278 (4): F659-66.
Pharmacological plasticity of cardiac ATP-sensitive potassium channels toward diazoxide revealed by ADP. , D'hahan N, Moreau C, Prost AL, Jacquet H, Alekseev AE, Terzic A, Vivaudou M., Proc Natl Acad Sci U S A. October 12, 1999; 96 (21): 12162-7.
Interaction of vanadate with the cloned beta cell K(ATP) channel. , Proks P, Ashfield R, Ashcroft FM., J Biol Chem. September 3, 1999; 274 (36): 25393-7.
A transmembrane domain of the sulfonylurea receptor mediates activation of ATP-sensitive K(+) channels by K(+) channel openers. , D'hahan N, Jacquet H, Moreau C, Catty P, Vivaudou M., Mol Pharmacol. August 1, 1999; 56 (2): 308-15.
Differential sensitivity of beta-cell and extrapancreatic K(ATP) channels to gliclazide. , Gribble FM, Ashcroft 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, Gribble FM, Ashcroft SJ, Ashcroft FM., Diabetes. June 1, 1999; 48 (6): 1341-7.
Tissue specificity of sulfonylureas: studies on cloned cardiac and beta-cell K(ATP) channels. , Gribble FM, Tucker SJ, Seino S, Ashcroft FM., Diabetes. September 1, 1998; 47 (9): 1412-8.