The Link Between Inactivation and High-Affinity Block of hERG1 Channels

Molecular Pharmacology- United States

doi 10.1124/mol.115.098111

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April 8, 2015

Authors

Wei Wu

Alison Gardner

Michael C. Sanguinetti

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

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The Link Between Inactivation and High-Affinity Block of hERG1 Channels

Molecular Pharmacology- United States

Full Text

Abstract

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Date

Authors

Publisher

Related search

A Link Between the E-Value and the Robustness of Block Designs

Molecular Determinants of High Affinity Phenylalkylamine Block of L-Type Calcium Channels in Transmembrane Segment IIIS6 and the Pore Region of the Α1Subunit

hERG1 Potassium Channels: Novel Biomarkers in Human Solid Cancers

Potent Block of Inactivation-Deficient Na+ Channels by N-3 Polyunsaturated Fatty Acids

Block of Inactivation-Deficient Na+Channels by Local Anesthetics in Stably Transfected Mammalian Cells

Steady-State Availability of Sodium Channels. Interactions Between Activation and Slow Inactivation

Introduction. The Blurred Boundary Between Channels and Transporters: We Dedicate This Volume to the Memory of Peter Lauger, a Pioneer of the Link Between Channels and Pumps.

Is There a Link Between Protein pICln and Volume-Regulated Anion Channels?

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