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Pharmacological Removal of Human Ether-Ã -go-go-Related Gene Potassium Channel Inactivation by 3-Nitro-N-(4-phenoxyphenyl) Benzamide (ICA-105574)

Molecular pharmacology, 2010-01, Vol.77 (1), p.58-68

2010

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Personalized medicine: Vinpocetine to reverse effects of GABRB3 mutation

Epilepsia (Copenhagen), 2019-12, Vol.60 (12), p.2459-2465

2019

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The KCNQ2/3 selective channel opener ICA-27243 binds to a novel voltage-sensor domain site

Neuroscience letters, 2009-11, Vol.465 (2), p.138-142

2009

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TRPA1 ankyrin repeat six interacts with a small molecule inhibitor chemotype

Proceedings of the National Academy of Sciences - PNAS, 2018-11, Vol.115 (48), p.12301-12306

2018

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Antiepileptic Drug Discovery and Development: What Have We Learned and Where Are We Going?

Pharmaceuticals, 2010-09, Vol.3 (9), p.2884-2899

2010

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A comprehensive approach to identifying repurposed drugs to treat SCN8A epilepsy

Epilepsia (Copenhagen), 2018-04, Vol.59 (4), p.802-813

2018

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A novel selective and orally bioavailable Nav1.8 channel blocker, PF‐01247324, attenuates nociception and sensory neuron excitability

British journal of pharmacology, 2015-05, Vol.172 (10), p.2654-2670

2015

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Trafficking of the Ca2+-activated K+Channel, hIK1, Is Dependent upon a C-terminal Leucine Zipper

The Journal of biological chemistry, 2003-03, Vol.278 (10), p.8476-8486

2003

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Validation of ion channel targets

Channels (Austin, Tex.), 2015-11, Vol.9 (6), p.376-379

2015

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Discovery of a Series of Indazole TRPA1 Antagonists

ACS medicinal chemistry letters, 2017-06, Vol.8 (6), p.666-671

2017

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Kinase-dependent Regulation of the Intermediate Conductance, Calcium-dependent Potassium Channel, hIK1

The Journal of biological chemistry, 2000-01, Vol.275 (1), p.585-598

2000

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Pharmacological activation of cloned intermediate- and small-conductance Ca2+-activated K+ channels

American Journal of Physiology: Cell Physiology, 2000-03, Vol.278 (3), p.C570

2000

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ATP-dependent Activation of the Intermediate Conductance, Ca2+-activated K+ Channel, hIK1, Is Conferred by a C-terminal Domain

The Journal of biological chemistry, 2001-04, Vol.276 (14), p.10963-10970

2001

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A comprehensive approach to identifying repurposed drugs to treat SCN 8A epilepsy

Epilepsia (Copenhagen), 2018-04, Vol.59 (4), p.802-813

2018

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A novel selective and orally bioavailable Na sub(v)1.8 channel blocker, PF-01247324, attenuates nociception and sensory neuron excitability

British journal of pharmacology, 2015-05, Vol.172 (10), p.2654-2670

2015

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A novel selective and orally bioavailable N a v 1.8 channel blocker, PF ‐01247324, attenuates nociception and sensory neuron excitability

British journal of pharmacology, 2015-05, Vol.172 (10), p.2654-2670

2015

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Pharmacological activation of cloned intermediate- and small-conductance Ca(2+)-activated K(+) channels

American Journal of Physiology: Cell Physiology, 2000-03, Vol.278 (3), p.C570-C581

2000

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Identification of a Potent hERG Channel Activator with a Novel Mechanism of Action

The FASEB journal, 2007-04, Vol.21 (5), p.A539-A539

2007

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CHAPTER 4 - Ion Channel Modulators

Pain therapeutics : current and future treatment paradigms, 2014, p.131-170

2014

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Inhibition of intestinal Cl- secretion by clotrimazole: direct effect on basolateral membrane K+ channels

American Journal of Physiology: Cell Physiology, 1997-08, Vol.273 (2), p.C531-C540

1997

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Stimulation of Cl(-) secretion by chlorzoxazone

The Journal of pharmacology and experimental therapeutics, 2000-02, Vol.292 (2), p.778

2000

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A novel selective and orally bioavailable Nav 1.8 channel blocker, PF-01247324, attenuates nociception and sensory neuron excitability

British journal of pharmacology, 2015-05, Vol.172 (10), p.2654

2015

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Pharmacological activation of cloned intermediate- and small-conductance Ca 2+ -activated K + channels

American Journal of Physiology: Cell Physiology, 2000-03, Vol.278 (3), p.C570-C581

2000

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Pharmacological activation of cloned intermediate-and small-conductance Ca2+-activated K+ channels

American Journal of Physiology: Cell Physiology, 2000-03, Vol.47 (3), p.C570-C581

2000

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Inhibition of intestinal Cl- secretion by clotrimazole : direct effect on basolateral membrane K+ channels

American Journal of Physiology: Cell Physiology, 1997-08, Vol.42 (2), p.C531-C540

1997

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Pharmacological Removal of Human Ether-Ã -go-go-Related Gene Potassium Channel Inactivation by 3-Nitro-N-(4-phenoxyphenyl) Benzamide (ICA-105574)

Personalized medicine: Vinpocetine to reverse effects of GABRB3 mutation

The KCNQ2/3 selective channel opener ICA-27243 binds to a novel voltage-sensor domain site

TRPA1 ankyrin repeat six interacts with a small molecule inhibitor chemotype

Antiepileptic Drug Discovery and Development: What Have We Learned and Where Are We Going?

A comprehensive approach to identifying repurposed drugs to treat SCN8A epilepsy

A novel selective and orally bioavailable Nav1.8 channel blocker, PF‐01247324, attenuates nociception and sensory neuron excitability

Trafficking of the Ca2+-activated K+Channel, hIK1, Is Dependent upon a C-terminal Leucine Zipper

Validation of ion channel targets

Discovery of a Series of Indazole TRPA1 Antagonists

Kinase-dependent Regulation of the Intermediate Conductance, Calcium-dependent Potassium Channel, hIK1

Pharmacological activation of cloned intermediate- and small-conductance Ca2+-activated K+ channels

ATP-dependent Activation of the Intermediate Conductance, Ca2+-activated K+ Channel, hIK1, Is Conferred by a C-terminal Domain

A comprehensive approach to identifying repurposed drugs to treat SCN 8A epilepsy

A novel selective and orally bioavailable Na sub(v)1.8 channel blocker, PF-01247324, attenuates nociception and sensory neuron excitability

A novel selective and orally bioavailable N a v 1.8 channel blocker, PF ‐01247324, attenuates nociception and sensory neuron excitability

Pharmacological activation of cloned intermediate- and small-conductance Ca(2+)-activated K(+) channels

Identification of a Potent hERG Channel Activator with a Novel Mechanism of Action

CHAPTER 4 - Ion Channel Modulators

Inhibition of intestinal Cl- secretion by clotrimazole: direct effect on basolateral membrane K+ channels

Stimulation of Cl(-) secretion by chlorzoxazone

A novel selective and orally bioavailable Nav 1.8 channel blocker, PF-01247324, attenuates nociception and sensory neuron excitability

Pharmacological activation of cloned intermediate- and small-conductance Ca 2+ -activated K + channels

Pharmacological activation of cloned intermediate-and small-conductance Ca2+-activated K+ channels

Inhibition of intestinal Cl- secretion by clotrimazole : direct effect on basolateral membrane K+ channels

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