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Identification of WP1066, an inhibitor of JAK2 and STAT3, as a K V 1.3 potassium channel blocker

British journal of pharmacology, 2021-07, Vol.178 (13), p.2617-2631

2021

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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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A new negative allosteric modulator, AP14145, for the study of small conductance calcium‐activated potassium (KCa2) channels

British journal of pharmacology, 2017-12, Vol.174 (23), p.4396-4408

2017

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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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Mechanism of inhibition of mouse Slo3 (KCa5.1) potassium channels by quinine, quinidine and barium

British journal of pharmacology, 2015-09, Vol.172 (17), p.4355-4363

2015

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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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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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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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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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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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4-Aminopyridine: a pan voltage-gated potassium channel inhibitor that enhances K v 7.4 currents and inhibits noradrenaline-mediated contraction of rat mesenteric small arteries

British journal of pharmacology, 2018-02, Vol.175 (3), p.501-516

2018

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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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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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Electrophysiological and functional effects of the KCNQ channel blocker XE991 on murine portal vein smooth muscle cells

British journal of pharmacology, 2005-10, Vol.146 (4), p.585-595

2005

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The cardiac persistent sodium current: an appealing therapeutic target?

British journal of pharmacology, 2008-03, Vol.153 (6), p.1133-1142

Saint, D A

2008

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Comparison of HERG channel blocking effects of various β‐blockers – implication for clinical strategy

British journal of pharmacology, 2006-03, Vol.147 (6), p.642-652

2006

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New tricks for old dogs: KCNQ expression and role in smooth muscle

British journal of pharmacology, 2009-04, Vol.156 (8), p.1196-1203

2009

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Identification of WP1066, an inhibitor of JAK2 and STAT3, as a K V 1.3 potassium channel blocker

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

A new negative allosteric modulator, AP14145, for the study of small conductance calcium‐activated potassium (KCa2) channels

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

Mechanism of inhibition of mouse Slo3 (KCa5.1) potassium channels by quinine, quinidine and barium

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

The high frequency relationship: implications for torsadogenic hERG blockers

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

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

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

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

4-Aminopyridine: a pan voltage-gated potassium channel inhibitor that enhances K v 7.4 currents and inhibits noradrenaline-mediated contraction of rat mesenteric small arteries

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

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

Electrophysiological and functional effects of the KCNQ channel blocker XE991 on murine portal vein smooth muscle cells

The cardiac persistent sodium current: an appealing therapeutic target?

Comparison of HERG channel blocking effects of various β‐blockers – implication for clinical strategy

New tricks for old dogs: KCNQ expression and role in smooth muscle

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