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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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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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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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Insect sodium channels and insecticide resistance

Invertebrate neuroscience, 2007-03, Vol.7 (1), p.17-30

Dong, Ke

2007

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Proarrhythmic mechanisms of the common anti-diarrheal medication loperamide: revelations from the opioid abuse epidemic

Naunyn-Schmiedeberg's archives of pharmacology, 2016-10, Vol.389 (10), p.1133-1137

2016

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Remarkable Phenytoin Sensitivity in 4 Children with SCN8A-related Epilepsy: A Molecular Neuropharmacological Approach

Neurotherapeutics, 2016-01, Vol.13 (1), p.192-197

2016

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Modulatory effects of bufalin, an active ingredient from toad venom on voltage-gated sodium channels

Molecular biology reports, 2018-10, Vol.45 (5), p.721-740

2018

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Late sodium current (INaL) in pancreatic β-cells

Pflügers Archiv, 2015-08, Vol.467 (8), p.1757-1768

2015

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The neonatal splice variant of Nav1.5 potentiates in vitro invasive behaviour of MDA-MB-231 human breast cancer cells

Breast cancer research and treatment, 2007-01, Vol.101 (2), p.149-160

2007

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Characterizing the effects of Eugenol on neuronal ionic currents and hyperexcitability

Psychopharmacologia, 2012-06, Vol.221 (4), p.575-587

2012

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The Role of Sodium Channels in Painful Diabetic and Idiopathic Neuropathy

Current diabetes reports, 2014-10, Vol.14 (10), p.538-538, Article 538

2014

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Tetrodotoxin-sensitive α-subunits of voltage-gated sodium channels are relevant for inhibition of cardiac sodium currents by local anesthetics

Naunyn-Schmiedeberg's archives of pharmacology, 2016-06, Vol.389 (6), p.625-636

2016

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Clopidogrel attenuates lithium-induced alterations in renal water and sodium channels/transporters in mice

Purinergic signalling, 2015-12, Vol.11 (4), p.507-518

2015

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Direct Activation of ENaC by Angiotensin II: Recent Advances and New Insights

Current hypertension reports, 2013-02, Vol.15 (1), p.17-24

2013

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Oxidation of multiple methionine residues impairs rapid sodium channel inactivation

Pflügers Archiv, 2008-09, Vol.456 (6), p.1085-1095

2008

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The Migratory Capacity of Human Trophoblastic BeWo Cells: Effects of Aldosterone and the Epithelial Sodium Channel

The Journal of membrane biology, 2013-03, Vol.246 (3), p.243-255

2013

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Remission of nephrotic syndrome diminishes urinary plasmin content and abolishes activation of ENaC

Pediatric nephrology (Berlin, West), 2013-08, Vol.28 (8), p.1227-1234

2013

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Effect of dronedarone on Na+, Ca2+ and HCN channels

Naunyn-Schmiedeberg's archives of pharmacology, 2011-04, Vol.383 (4), p.347-356

2011

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Response to Carbamazepine in KCNQ2 Related Early Infantile Epileptic Encephalopathy

Indian journal of pediatrics, 2019-03, Vol.86 (3), p.301-302

2019

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Polyunsaturated Fatty Acid Modulation of Voltage-Gated Ion Channels

Cell biochemistry and biophysics, 2008-10, Vol.52 (2), p.59-84

2008

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Brain natriuretic peptide suppresses pain induced by BmK I, a sodium channel-specific modulator, in rats

Journal of headache and pain, 2016-12, Vol.17 (1), p.90-15, Article 90

2016

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Long-term modulation of Na+ and K+ channels by TGF-β1 in neonatal rat cardiac myocytes

Pflügers Archiv, 2011-02, Vol.461 (2), p.235-247

2011

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Tetrodotoxin blocks L-type Ca2+ channels in canine ventricular cardiomyocytes

Pflügers Archiv, 2012-08, Vol.464 (2), p.167-174

2012

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Peptide toxins in sea anemones: structural and functional aspects

Marine biotechnology (New York, N.Y.), 2006-01, Vol.8 (1), p.1-10

2006

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Brevenal is a natural inhibitor of brevetoxin action in sodium channel receptor binding assays

Cellular and molecular neurobiology, 2004-08, Vol.24 (4), p.553-563

2004

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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

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

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

Insect sodium channels and insecticide resistance

Proarrhythmic mechanisms of the common anti-diarrheal medication loperamide: revelations from the opioid abuse epidemic

Remarkable Phenytoin Sensitivity in 4 Children with SCN8A-related Epilepsy: A Molecular Neuropharmacological Approach

Modulatory effects of bufalin, an active ingredient from toad venom on voltage-gated sodium channels

Late sodium current (INaL) in pancreatic β-cells

The neonatal splice variant of Nav1.5 potentiates in vitro invasive behaviour of MDA-MB-231 human breast cancer cells

Characterizing the effects of Eugenol on neuronal ionic currents and hyperexcitability

The Role of Sodium Channels in Painful Diabetic and Idiopathic Neuropathy

Tetrodotoxin-sensitive α-subunits of voltage-gated sodium channels are relevant for inhibition of cardiac sodium currents by local anesthetics

Clopidogrel attenuates lithium-induced alterations in renal water and sodium channels/transporters in mice

Direct Activation of ENaC by Angiotensin II: Recent Advances and New Insights

Oxidation of multiple methionine residues impairs rapid sodium channel inactivation

The Migratory Capacity of Human Trophoblastic BeWo Cells: Effects of Aldosterone and the Epithelial Sodium Channel

Remission of nephrotic syndrome diminishes urinary plasmin content and abolishes activation of ENaC

Effect of dronedarone on Na+, Ca2+ and HCN channels

Response to Carbamazepine in KCNQ2 Related Early Infantile Epileptic Encephalopathy

Polyunsaturated Fatty Acid Modulation of Voltage-Gated Ion Channels

Brain natriuretic peptide suppresses pain induced by BmK I, a sodium channel-specific modulator, in rats

Long-term modulation of Na+ and K+ channels by TGF-β1 in neonatal rat cardiac myocytes

Tetrodotoxin blocks L-type Ca2+ channels in canine ventricular cardiomyocytes

Peptide toxins in sea anemones: structural and functional aspects

Brevenal is a natural inhibitor of brevetoxin action in sodium channel receptor binding assays

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