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A novel, potent, and selective inhibitor of cardiac late sodium current suppresses experimental arrhythmias

The Journal of pharmacology and experimental therapeutics, 2013-01, Vol.344 (1), p.23

2013

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Engineering a Stable and Selective Peptide Blocker of the Kv1.3 Channel in T Lymphocytes

Molecular pharmacology, 2009-04, Vol.75 (4), p.762-773

2009

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Durable pharmacological responses from the peptide ShK-186, a specific Kv1.3 channel inhibitor that suppresses T cell mediators of autoimmune disease

The Journal of pharmacology and experimental therapeutics, 2012-09, Vol.342 (3), p.642

2012

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Withaferin A suppresses breast cancer cell proliferation by inhibition of the two-pore domain potassium (K2P9) channel TASK-3

Biomedicine & pharmacotherapy, 2020-09, Vol.129, p.110383-110383, Article 110383

2020

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Inhibition of cardiac K v 4.3 (I to ) channel isoforms by class I antiarrhythmic drugs lidocaine and mexiletine

European journal of pharmacology, 2020-08, Vol.880, p.173159

2020

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The Small Conductance Calcium-Activated Potassium Channel Inhibitors NS8593 and UCL1684 Prevent the Development of Atrial Fibrillation Through Atrial-Selective Inhibition of Sodium Channel Activity

Journal of cardiovascular pharmacology, 2020-08, Vol.76 (2), p.164

2020

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Vm24, a natural immunosuppressive peptide, potently and selectively blocks Kv1.3 potassium channels of human T cells

Molecular pharmacology, 2012-09, Vol.82 (3), p.372-382

2012

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Characterization of VU0468554, a New Selective Inhibitor of Cardiac G Protein-Gated Inwardly Rectifying K + Channels

Molecular pharmacology, 2021-12, Vol.100 (6), p.540-547

2021

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Participation of potassium channels in the antinociceptive effect of docosahexaenoic acid in the rat formalin test

European journal of pharmacology, 2016-12, Vol.793, p.95-100

2016

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GPER agonist dilates mesenteric arteries via PI3K-Akt-eNOS and potassium channels in both sexes

Life Sciences, 2017-08, Vol.183, p.21-27

2017

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Chronic heart failure increases negative chronotropic effects of adenosine in canine sinoatrial cells via A1R stimulation and GIRK-mediated I Kado

Life sciences (1973), 2020-01, Vol.240, p.117068

2020

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Isolation of proflavine as a blocker of G protein-gated inward rectifier potassium channels by a cell growth-based screening system

Neuropharmacology, 2016-10, Vol.109, p.18-28

2016

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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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Isolation and characterization of Ts19 Fragment II, a new long-chain potassium channel toxin from Tityus serrulatus venom

Peptides (New York, N.Y. : 1980), 2016-06, Vol.80, p.9-17

2016

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Glibenclamide inhibits NLRP3 inflammasome-mediated IL-1β secretion in human trophoblasts

Journal of pharmacological sciences, 2017-10, Vol.135 (2), p.89-95

2017

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A Model of the Block of Voltage-Gated Potassium Kv4.2 Ionic Currents by 4-Aminopyridine

The Journal of pharmacology and experimental therapeutics, 2017-11, Vol.363 (2), p.184

Kehl, Steven J

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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The role of voltage-gated potassium channels Kv2.1 and Kv2.2 in the regulation of insulin and somatostatin release from pancreatic islets

The Journal of pharmacology and experimental therapeutics, 2013-02, Vol.344 (2), p.407

2013

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

Molecular pharmacology, 2015-06, Vol.87 (6), p.1042-1050

2015

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Elucidation of the possible mechanism of analgesic action of methanol stem bark extract of Uapaca togoensis pax in mice

Journal of ethnopharmacology, 2019-12, Vol.245, p.112156-112156, Article 112156

2019

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Pharmacologic inhibition of the renal outer medullary potassium channel causes diuresis and natriuresis in the absence of kaliuresis

The Journal of pharmacology and experimental therapeutics, 2014-01, Vol.348 (1), p.153

2014

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Anti-addiction drug ibogaine inhibits voltage-gated ionic currents: A study to assess the drug's cardiac ion channel profile

Toxicology and applied pharmacology, 2013-12, Vol.273 (2), p.259-268

2013

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Design of PAP-1, a Selective Small Molecule Kv1.3 Blocker, for the Suppression of Effector Memory T Cells in Autoimmune Diseases

Molecular pharmacology, 2005-11, Vol.68 (5), p.1254-1270

2005

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A novel, potent, and selective inhibitor of cardiac late sodium current suppresses experimental arrhythmias

Engineering a Stable and Selective Peptide Blocker of the Kv1.3 Channel in T Lymphocytes

Durable pharmacological responses from the peptide ShK-186, a specific Kv1.3 channel inhibitor that suppresses T cell mediators of autoimmune disease

Withaferin A suppresses breast cancer cell proliferation by inhibition of the two-pore domain potassium (K2P9) channel TASK-3

Inhibition of cardiac K v 4.3 (I to ) channel isoforms by class I antiarrhythmic drugs lidocaine and mexiletine

Discovery of (3-(4-(2-Oxa-6-azaspiro[3.3]heptan-6-ylmethyl)phenoxy)azetidin-1-yl)(5-(4-methoxyphenyl)-1,3,4-oxadiazol-2-yl)methanone (AZD1979), a Melanin Concentrating Hormone Receptor 1 (MCHr1) Antagonist with Favorable Physicochemical Properties

The Small Conductance Calcium-Activated Potassium Channel Inhibitors NS8593 and UCL1684 Prevent the Development of Atrial Fibrillation Through Atrial-Selective Inhibition of Sodium Channel Activity

Vm24, a natural immunosuppressive peptide, potently and selectively blocks Kv1.3 potassium channels of human T cells

Characterization of VU0468554, a New Selective Inhibitor of Cardiac G Protein-Gated Inwardly Rectifying K + Channels

Participation of potassium channels in the antinociceptive effect of docosahexaenoic acid in the rat formalin test

GPER agonist dilates mesenteric arteries via PI3K-Akt-eNOS and potassium channels in both sexes

Chronic heart failure increases negative chronotropic effects of adenosine in canine sinoatrial cells via A1R stimulation and GIRK-mediated I Kado

Isolation of proflavine as a blocker of G protein-gated inward rectifier potassium channels by a cell growth-based screening system

The high frequency relationship: implications for torsadogenic hERG blockers

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

Isolation and characterization of Ts19 Fragment II, a new long-chain potassium channel toxin from Tityus serrulatus venom

Glibenclamide inhibits NLRP3 inflammasome-mediated IL-1β secretion in human trophoblasts

A Model of the Block of Voltage-Gated Potassium Kv4.2 Ionic Currents by 4-Aminopyridine

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

The role of voltage-gated potassium channels Kv2.1 and Kv2.2 in the regulation of insulin and somatostatin release from pancreatic islets

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

Elucidation of the possible mechanism of analgesic action of methanol stem bark extract of Uapaca togoensis pax in mice

Pharmacologic inhibition of the renal outer medullary potassium channel causes diuresis and natriuresis in the absence of kaliuresis

Anti-addiction drug ibogaine inhibits voltage-gated ionic currents: A study to assess the drug's cardiac ion channel profile

Design of PAP-1, a Selective Small Molecule Kv1.3 Blocker, for the Suppression of Effector Memory T Cells in Autoimmune Diseases

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