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Neurosteroids Allopregnanolone Sulfate and Pregnanolone Sulfate Have Diverse Effect on the α Subunit of the Neuronal Voltage-gated Sodium Channels Nav1.2, Nav1.6, Nav1.7, and Nav1.8 Expressed in Xenopus Oocytes

Anesthesiology (Philadelphia), 2014-09, Vol.121 (3), p.620-631

2014

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Modulation of peripheral Na+ channels and neuronal firing by n-butyl-p-aminobenzoate

European journal of pharmacology, 2014-03, Vol.727, p.158-166

2014

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Blocking voltage-gated sodium channels as a strategy to suppress pathological cough

Pulmonary pharmacology & therapeutics, 2017-12, Vol.47, p.38-41

2017

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Antidepressants inhibit Na v 1.3, Na v 1.7, and Na v 1.8 neuronal voltage-gated sodium channels more potently than Na v 1.2 and Na v 1.6 channels expressed in Xenopus oocytes

Naunyn-Schmiedeberg's archives of pharmacology, 2017-12, Vol.390 (12), p.1255

2017

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Expression of sodium channel α subunits 1.1, 1.2 and 1.6 in rat hippocampus after kainic acid-induced epilepsy

Epilepsy research, 2013-09, Vol.106 (1), p.17-28

2013

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Mechanism and molecular basis for the sodium channel subtype specificity of µ‐conopeptide CnIIIC

British journal of pharmacology, 2012-10, Vol.167 (3), p.576-586

2012

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Sevoflurane modulation of tetrodotoxin-resistant Na+ channels in small-sized dorsal root ganglion neurons of rats

Neuroreport, 2021-12, Vol.32 (17), p.1335

2021

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High-throughput screening against protein:protein interaction interfaces reveals anti-cancer therapeutics as potent modulators of the voltage-gated Na + channel complex

Scientific reports, 2019-11, Vol.9 (1), p.16890-15, Article 16890

2019

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Sidedness of carbamazepine accessibility to voltage-gated sodium channels

Molecular pharmacology, 2014-02, Vol.85 (2), p.381-387

2014

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Inhibition of the late sodium current slows t-tubule disruption during the progression of hypertensive heart disease in the rat

American journal of physiology. Heart and circulatory physiology, 2013-10, Vol.305 (7), p.H1068-H1079

2013

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Arachidonic acid potentiates acid-sensing ion channels in rat sensory neurons by a direct action

Neuroscience, 2007-03, Vol.145 (2), p.686-698

2007

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Comprehensive engineering of the tarantula venom peptide huwentoxin-IV to inhibit the human voltage-gated sodium channel hNa v 1.7

The Journal of biological chemistry, 2020-01, Vol.295 (5), p.1315-1327

2020

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To4, the first Tityus obscurus β-toxin fully electrophysiologically characterized on human sodium channel isoforms

Peptides (New York, N.Y. : 1980), 2017-09, Vol.95, p.106-115

2017

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The opioid methadone induces a local anaesthetic-like inhibition of the cardiac Na⁺ channel, Na(v)1.5

British journal of pharmacology, 2014-01, Vol.171 (2), p.427

2014

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Development of a Rapid Throughput Assay for Identification of hNav1.7 Antagonist Using Unique Efficacious Sodium Channel Agonist, Antillatoxin

Marine drugs, 2016-02, Vol.14 (2), p.36

2016

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Structure and Pharmacology of Voltage-Gated Sodium and Calcium Channels

Annual review of pharmacology and toxicology, 2020-01, Vol.60, p.133

2020

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Differential modulation of Nav1.7 and Nav1.8 channels by antidepressant drugs

European journal of pharmacology, 2015-10, Vol.764, p.395-403

2015

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Pharmacological and electrophysiological characterization of the human bile acid-sensitive ion channel (hBASIC)

Pflügers Archiv, 2014-02, Vol.466 (2), p.253-263

2014

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International Union of Basic and Clinical Pharmacology. XCI. structure, function, and pharmacology of acid-sensing ion channels and the epithelial Na+ channel

Pharmacological reviews, 2015-01, Vol.67 (1), p.1-35

2015

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Targeting voltage gated sodium channels NaV1.7, Na V1.8, and Na V1.9 for treatment of pathological cough

Lung, 2014-02, Vol.192 (1), p.15

2014

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Regulation of SCN3B/scn3b by Interleukin 2 (IL-2): IL-2 modulates SCN3B/scn3b transcript expression and increases sodium current in myocardial cells

BMC cardiovascular disorders, 2016-01, Vol.16 (1), p.1-1, Article 1

2016

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Dynamical characterization of inactivation path in voltage-gated Na+ ion channel by non-equilibrium response spectroscopy

Channels (Austin, Tex.), 2016-11, Vol.10 (6), p.478-497

2016

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Kinetic Analysis of Membrane Potential Dye Response to NaV1.7 Channel Activation Identifies Antagonists with Pharmacological Selectivity against NaV1.5

Journal of biomolecular screening, 2016-06, Vol.21 (5), p.480-489

2016

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A purified Palythoa venom fraction delays sodium current inactivation in sympathetic neurons

Toxicon (Oxford), 2014-05, Vol.82, p.112-116

2014

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Status of peripheral sodium channel blockers for non-addictive pain treatment

Nature reviews. Neurology, 2020-12, Vol.16 (12), p.689-705

2020

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Neurosteroids Allopregnanolone Sulfate and Pregnanolone Sulfate Have Diverse Effect on the α Subunit of the Neuronal Voltage-gated Sodium Channels Nav1.2, Nav1.6, Nav1.7, and Nav1.8 Expressed in Xenopus Oocytes

Modulation of peripheral Na+ channels and neuronal firing by n-butyl-p-aminobenzoate

Blocking voltage-gated sodium channels as a strategy to suppress pathological cough

Antidepressants inhibit Na v 1.3, Na v 1.7, and Na v 1.8 neuronal voltage-gated sodium channels more potently than Na v 1.2 and Na v 1.6 channels expressed in Xenopus oocytes

Expression of sodium channel α subunits 1.1, 1.2 and 1.6 in rat hippocampus after kainic acid-induced epilepsy

Mechanism and molecular basis for the sodium channel subtype specificity of µ‐conopeptide CnIIIC

Sevoflurane modulation of tetrodotoxin-resistant Na+ channels in small-sized dorsal root ganglion neurons of rats

High-throughput screening against protein:protein interaction interfaces reveals anti-cancer therapeutics as potent modulators of the voltage-gated Na + channel complex

Sidedness of carbamazepine accessibility to voltage-gated sodium channels

Inhibition of the late sodium current slows t-tubule disruption during the progression of hypertensive heart disease in the rat

Arachidonic acid potentiates acid-sensing ion channels in rat sensory neurons by a direct action

Comprehensive engineering of the tarantula venom peptide huwentoxin-IV to inhibit the human voltage-gated sodium channel hNa v 1.7

To4, the first Tityus obscurus β-toxin fully electrophysiologically characterized on human sodium channel isoforms

The opioid methadone induces a local anaesthetic-like inhibition of the cardiac Na⁺ channel, Na(v)1.5

Development of a Rapid Throughput Assay for Identification of hNav1.7 Antagonist Using Unique Efficacious Sodium Channel Agonist, Antillatoxin

Structure and Pharmacology of Voltage-Gated Sodium and Calcium Channels

Differential modulation of Nav1.7 and Nav1.8 channels by antidepressant drugs

Pharmacological and electrophysiological characterization of the human bile acid-sensitive ion channel (hBASIC)

International Union of Basic and Clinical Pharmacology. XCI. structure, function, and pharmacology of acid-sensing ion channels and the epithelial Na+ channel

Targeting voltage gated sodium channels NaV1.7, Na V1.8, and Na V1.9 for treatment of pathological cough

Regulation of SCN3B/scn3b by Interleukin 2 (IL-2): IL-2 modulates SCN3B/scn3b transcript expression and increases sodium current in myocardial cells

Dynamical characterization of inactivation path in voltage-gated Na+ ion channel by non-equilibrium response spectroscopy

Kinetic Analysis of Membrane Potential Dye Response to NaV1.7 Channel Activation Identifies Antagonists with Pharmacological Selectivity against NaV1.5

A purified Palythoa venom fraction delays sodium current inactivation in sympathetic neurons

Status of peripheral sodium channel blockers for non-addictive pain treatment

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