Intracellular nucleotide-mediated gating of SUR/Kir6.0 complex potassium channels expressed in a mammalian cell line and its modification by pinacidil. (Q41014158)

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scientific article published on September 1998

Language	Label	Description	Also known as
English	Intracellular nucleotide-mediated gating of SUR/Kir6.0 complex potassium channels expressed in a mammalian cell line and its modification by pinacidil.	scientific article published on September 1998

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scholarly article

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3 December 2019

Intracellular nucleotide-mediated gating of SUR/Kir6.0 complex potassium channels expressed in a mammalian cell line and its modification by pinacidil (English)

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3 December 2019

Yoshiyuki Horio

5

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E Satoh

1

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M Yamada

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C Kondo

3

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V P Repunte

4

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T Iijima

6

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Y Kurachi

7

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1 September 1998

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3 December 2019

Journal of Physiology

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511 ( Pt 3)

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663-674

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3 December 2019

The effects of nucleotides and potassium channel openers on the SUR2A/Kir6.2 complex K+ channel expressed in a mammalian cell line, HEK293T cells.

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Regulation of KATP channel activity by diazoxide and MgADP. Distinct functions of the two nucleotide binding folds of the sulfonylurea receptor

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Truncation of Kir6.2 produces ATP-sensitive K+ channels in the absence of the sulphonylurea receptor

1 reference

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The essential role of the Walker A motifs of SUR1 in K-ATP channel activation by Mg-ADP and diazoxide

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Sulphonylurea receptor 2B and Kir6.1 form a sulphonylurea-sensitive but ATP-insensitive K+ channel

1 reference

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A functional model for G protein activation of the muscarinic K+ channel in guinea pig atrial myocytes. Spectral analysis of the effect of GTP on single-channel kinetics

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A novel sulfonylurea receptor forms with BIR (Kir6.2) a smooth muscle type ATP-sensitive K+ channel

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A family of sulfonylurea receptors determines the pharmacological properties of ATP-sensitive K+ channels

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Cloning and functional expression of the cDNA encoding a novel ATP-sensitive potassium channel subunit expressed in pancreatic beta-cells, brain, heart and skeletal muscle

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The pharmacology of ATP-sensitive potassium channels

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K channel activation by nucleotide diphosphates and its inhibition by glibenclamide in vascular smooth muscle cells

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Cloning and functional characterization of a novel ATP-sensitive potassium channel ubiquitously expressed in rat tissues, including pancreatic islets, pituitary, skeletal muscle, and heart

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Physiological roles and properties of potassium channels in arterial smooth muscle

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Cloning of the beta cell high-affinity sulfonylurea receptor: a regulator of insulin secretion

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Cardiac ATP-sensitive K+ channels: regulation by intracellular nucleotides and K+ channel-opening drugs

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Reconstitution of IKATP: an inward rectifier subunit plus the sulfonylurea receptor

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Isomeric equilibria in complexes of adenosine 5'-triphosphate with divalent metal ions. Solution structures of M(ATP)2- complexes

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Adenosine 5'-triphosphate-sensitive potassium channels

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Guanosine diphosphate activates an adenosine 5'-triphosphate-sensitive K+ channel in the rabbit portal vein

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Identifiers

10.1111/J.1469-7793.1998.663BG.X

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3 December 2019

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