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Neural KCNQ (Kv7) channels

British journal of pharmacology, 2009-04, Vol.156 (8), p.1185-1195

2009

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Targeting two‐pore domain K+ channels TREK‐1 and TASK‐3 for the treatment of depression: a new therapeutic concept

British journal of pharmacology, 2015-02, Vol.172 (3), p.771-784

2015

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Multiple targets for flecainide action: implications for cardiac arrhythmogenesis

British journal of pharmacology, 2018-04, Vol.175 (8), p.1260-1278

2018

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Understanding and improving photo‐control of ion channels in nociceptors with azobenzene photo‐switches

British journal of pharmacology, 2018-06, Vol.175 (12), p.2296-2311

2018

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Computational assessment of drug‐induced effects on the electrocardiogram: from ion channel to body surface potentials

British journal of pharmacology, 2013-02, Vol.168 (3), p.718-733

2013

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NS6180, a new K(Ca) 3.1 channel inhibitor prevents T-cell activation and inflammation in a rat model of inflammatory bowel disease

British journal of pharmacology, 2013-01, Vol.168 (2), p.432

2013

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Characterization of a novel multifunctional resveratrol derivative for the treatment of atrial fibrillation

British journal of pharmacology, 2014-01, Vol.171 (1), p.92-106

2014

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Inhibition of human ether-à-go-go-related gene K+ currents expressed in HEK293 cells by three gingerol components from ginger

Journal of pharmacy and pharmacology, 2022-08, Vol.74 (8), p.1133-1139

2022

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Geraniol Blocks Calcium and Potassium Channels in the Mammalian Myocardium: Useful Effects to Treat Arrhythmias

Basic & clinical pharmacology & toxicology, 2014-12, Vol.115 (6), p.534-544

2014

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Modulation of vascular function by perivascular adipose tissue: the role of endothelium and hydrogen peroxide

British journal of pharmacology, 2007-06, Vol.151 (3), p.323-331

2007

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The high frequency relationship: implications for torsadogenic hERG blockers

British journal of pharmacology, 2016-02, Vol.173 (3), p.601-612

2016

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Molecular expression and pharmacological identification of a role for K(v)7 channels in murine vascular reactivity

British journal of pharmacology, 2007-07, Vol.151 (6), p.758-770

2007

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Clemizole hydrochloride blocks cardiac potassium currents stably expressed in HEK 293 cells

British journal of pharmacology, 2017-02, Vol.174 (3), p.254-266

2017

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Comparison of the IKr blockers moxifloxacin, dofetilide and E‐4031 in five screening models of pro‐arrhythmia reveals lack of specificity of isolated cardiomyocytes

British journal of pharmacology, 2012-01, Vol.165 (2), p.467-478

2012

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Exploring the Pharmacology and Action Spectra of Photochromic Open-Channel Blockers

Chembiochem : a European journal of chemical biology, 2012-08, Vol.13 (12), p.1746-1749

2012

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Functional expression of KCNQ (Kv7) channels in guinea pig bladder smooth muscle and their contribution to spontaneous activity

British journal of pharmacology, 2013-07, Vol.169 (6), p.1290-1304

2013

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Allosteric effects of erythromycin pretreatment on thioridazine block of hERG potassium channels

British journal of pharmacology, 2014-04, Vol.171 (7), p.1668-1675

Crumb, W J

2014

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Voltage-operated potassium (Kv) channels contribute to endothelium-dependent vasorelaxation of carvacrol on rat aorta

Journal of pharmacy and pharmacology, 2016-09, Vol.68 (9), p.1177-1183

2016

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Aldosterone down‐regulates the slowly activated delayed rectifier potassium current in adult guinea pig cardiomyocytes

British journal of pharmacology, 2015-12, Vol.172 (23), p.5596-5608

2015

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Structure‐activity relationships of pentamidine‐affected ion channel trafficking and dofetilide mediated rescue

British journal of pharmacology, 2013-07, Vol.169 (6), p.1322-1334

2013

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Inhibition of the human two‐pore domain potassium channel, TREK‐1, by fluoxetine and its metabolite norfluoxetine

British journal of pharmacology, 2005-03, Vol.144 (6), p.821-829

2005

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Discovery of a Pharmacologically Active Antagonist of the Two-Pore-Domain Potassium Channel K2P9.1 (TASK-3)

ChemMedChem, 2012-01, Vol.7 (1), p.123-133

2012

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Inhibition of the voltage‐dependent K+ current by the class Ic antiarrhythmic drug flecainide in rabbit coronary arterial smooth muscle cells

Clinical and experimental pharmacology & physiology, 2018-12, Vol.45 (12), p.1286-1292

2018

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Prospective Validation of a Comprehensive In silico hERG Model and its Applications to Commercial Compound and Drug Databases

ChemMedChem, 2010-05, Vol.5 (5), p.716-729

2010

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Tannic acid activates the Kv7.4 and Kv7.3/7.5 K+ channels expressed in HEK293 cells and reduces tension in the rat mesenteric arteries

Journal of pharmacy and pharmacology, 2016-04, Vol.68 (4), p.494-502

2016

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Neural KCNQ (Kv7) channels

Targeting two‐pore domain K+ channels TREK‐1 and TASK‐3 for the treatment of depression: a new therapeutic concept

Multiple targets for flecainide action: implications for cardiac arrhythmogenesis

Understanding and improving photo‐control of ion channels in nociceptors with azobenzene photo‐switches

Computational assessment of drug‐induced effects on the electrocardiogram: from ion channel to body surface potentials

NS6180, a new K(Ca) 3.1 channel inhibitor prevents T-cell activation and inflammation in a rat model of inflammatory bowel disease

Characterization of a novel multifunctional resveratrol derivative for the treatment of atrial fibrillation

Inhibition of human ether-à-go-go-related gene K+ currents expressed in HEK293 cells by three gingerol components from ginger

Geraniol Blocks Calcium and Potassium Channels in the Mammalian Myocardium: Useful Effects to Treat Arrhythmias

Modulation of vascular function by perivascular adipose tissue: the role of endothelium and hydrogen peroxide

The high frequency relationship: implications for torsadogenic hERG blockers

Molecular expression and pharmacological identification of a role for K(v)7 channels in murine vascular reactivity

Clemizole hydrochloride blocks cardiac potassium currents stably expressed in HEK 293 cells

Comparison of the IKr blockers moxifloxacin, dofetilide and E‐4031 in five screening models of pro‐arrhythmia reveals lack of specificity of isolated cardiomyocytes

Exploring the Pharmacology and Action Spectra of Photochromic Open-Channel Blockers

Functional expression of KCNQ (Kv7) channels in guinea pig bladder smooth muscle and their contribution to spontaneous activity

Allosteric effects of erythromycin pretreatment on thioridazine block of hERG potassium channels

Voltage-operated potassium (Kv) channels contribute to endothelium-dependent vasorelaxation of carvacrol on rat aorta

Aldosterone down‐regulates the slowly activated delayed rectifier potassium current in adult guinea pig cardiomyocytes

Structure‐activity relationships of pentamidine‐affected ion channel trafficking and dofetilide mediated rescue

Inhibition of the human two‐pore domain potassium channel, TREK‐1, by fluoxetine and its metabolite norfluoxetine

Discovery of a Pharmacologically Active Antagonist of the Two-Pore-Domain Potassium Channel K2P9.1 (TASK-3)

Inhibition of the voltage‐dependent K+ current by the class Ic antiarrhythmic drug flecainide in rabbit coronary arterial smooth muscle cells

Prospective Validation of a Comprehensive In silico hERG Model and its Applications to Commercial Compound and Drug Databases

Tannic acid activates the Kv7.4 and Kv7.3/7.5 K+ channels expressed in HEK293 cells and reduces tension in the rat mesenteric arteries

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