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Kv1.5 blockers preferentially inhibit TASK-1 channels: TASK-1 as a target against atrial fibrillation and obstructive sleep apnea?

Pflügers Archiv, 2015-05, Vol.467 (5), p.1081-1090

2015

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Endothelium-derived hyperpolarising factors and associated pathways: a synopsis

Pflügers Archiv, 2010-05, Vol.459 (6), p.863-879

2010

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Potassium channels in the Cx43 gap junction perinexus modulate ephaptic coupling: an experimental and modeling study

Pflügers Archiv, 2016-10, Vol.468 (10), p.1651-1661

2016

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Benzenesulfonamides act as open-channel blockers on K V 3.1 potassium channel

Amino acids, 2019-02, Vol.51 (2), p.355

2019

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Intracellular Binding of Terfenadine Competes with Its Access to Pancreatic ß-cell ATP-Sensitive K+ Channels and Human ether-à-go-go-Related Gene Channels

The Journal of membrane biology, 2023-02, Vol.256 (1), p.63-77

2023

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Physicochemical QSAR analysis of hERG inhibition revisited: towards a quantitative potency prediction

Journal of computer-aided molecular design, 2022-12, Vol.36 (12), p.837-849

2022

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Inward rectifier potassium current (IK1) and Kir2 composition of the zebrafish (Danio rerio) heart

Pflügers Archiv, 2015-12, Vol.467 (12), p.2437-2446

2015

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Complexes of Peptide Blockers with Kv1.6 Pore Domain: Molecular Modeling and Studies with KcsA-Kv1.6 Channel

Journal of neuroimmune pharmacology, 2017-06, Vol.12 (2), p.260-276

2017

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Characterization and functional roles of KCNQ-encoded voltage-gated potassium (Kv7) channels in human corpus cavernosum smooth muscle

Pflügers Archiv, 2020, Vol.472 (1), p.89-102

2020

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Dronedarone blockage of the tumor-related Kv10.1 channel: a comparison with amiodarone

Pflügers Archiv, 2020, Vol.472 (1), p.75-87

2020

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Fampridine for gait imbalance in patients with multiple sclerosis (MS): a systematic review and meta-analysis

Neurological sciences, 2023-09, Vol.44 (9), p.3059-3069

2023

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Kv1.3 channels modulate human vascular smooth muscle cells proliferation independently of mTOR signaling pathway

Pflügers Archiv, 2015-08, Vol.467 (8), p.1711-1722

2015

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Epoxyeicosatrienoic acids and endothelium-dependent responses

Pflügers Archiv, 2010-05, Vol.459 (6), p.881-895

2010

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Inhibitory effects of N-methyl-D-aspartate (NMDA) and α 1 -adrenergic receptor antagonist ifenprodil on human Kv1.5 channel

Naunyn-Schmiedeberg's archives of pharmacology, 2023-11, Vol.396 (11), p.3149

2023

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Escitalopram block of hERG potassium channels

Naunyn-Schmiedeberg's archives of pharmacology, 2014, Vol.387 (1), p.23-32

2014

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Vacuolar ion channels in the liverwort Marchantia polymorpha: influence of ion channel inhibitors

Planta, 2017-05, Vol.245 (5), p.1049-1060

2017

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Combined transcriptomic and proteomic analysis reveals a diversity of venom-related and toxin-like peptides expressed in the mat anemone Zoanthus natalensis (Cnidaria, Hexacorallia)

Archives of toxicology, 2019-06, Vol.93 (6), p.1745-1767

2019

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Mitochondrial KATP channel involvement in angiotensin II-induced autophagy in vascular smooth muscle cells

Basic research in cardiology, 2014-07, Vol.109 (4), p.416, Article 416

2014

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Fampridine is a Substrate and Inhibitor of Human OCT2, but not of Human MATE1, or MATE2K

Pharmaceutical research, 2018-08, Vol.35 (8), p.159-8, Article 159

2018

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Contribution of ion currents to beat-to-beat variability of action potential duration in canine ventricular myocytes

Pflügers Archiv, 2015-07, Vol.467 (7), p.1431-1443

2015

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Sustained-released fampridine in multiple sclerosis: effects on gait parameters, arm function, fatigue, and quality of life

Journal of neurology, 2015-08, Vol.262 (8), p.1936-1945

2015

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Novel electrophysiological properties of dronedarone: inhibition of human cardiac two-pore-domain potassium (K2P) channels

Naunyn-Schmiedeberg's archives of pharmacology, 2012-10, Vol.385 (10), p.1003-1016

2012

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Compilation and physicochemical classification analysis of a diverse hERG inhibition database

Journal of computer-aided molecular design, 2016-12, Vol.30 (12), p.1175-1188

2016

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Hydrogen peroxide induces vasorelaxation by enhancing 4-aminopyridine-sensitive Kv currents through S-glutathionylation

Pflügers Archiv, 2015-02, Vol.467 (2), p.285-297

2015

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The role of KCa3.1 channels in cardiac fibrosis induced by pressure overload in rats

Pflügers Archiv, 2015-11, Vol.467 (11), p.2275-2285

2015

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Kv1.5 blockers preferentially inhibit TASK-1 channels: TASK-1 as a target against atrial fibrillation and obstructive sleep apnea?

Endothelium-derived hyperpolarising factors and associated pathways: a synopsis

Potassium channels in the Cx43 gap junction perinexus modulate ephaptic coupling: an experimental and modeling study

Benzenesulfonamides act as open-channel blockers on K V 3.1 potassium channel

Intracellular Binding of Terfenadine Competes with Its Access to Pancreatic ß-cell ATP-Sensitive K+ Channels and Human ether-à-go-go-Related Gene Channels

Physicochemical QSAR analysis of hERG inhibition revisited: towards a quantitative potency prediction

Inward rectifier potassium current (IK1) and Kir2 composition of the zebrafish (Danio rerio) heart

Complexes of Peptide Blockers with Kv1.6 Pore Domain: Molecular Modeling and Studies with KcsA-Kv1.6 Channel

Characterization and functional roles of KCNQ-encoded voltage-gated potassium (Kv7) channels in human corpus cavernosum smooth muscle

Dronedarone blockage of the tumor-related Kv10.1 channel: a comparison with amiodarone

Fampridine for gait imbalance in patients with multiple sclerosis (MS): a systematic review and meta-analysis

Kv1.3 channels modulate human vascular smooth muscle cells proliferation independently of mTOR signaling pathway

Epoxyeicosatrienoic acids and endothelium-dependent responses

Inhibitory effects of N-methyl-D-aspartate (NMDA) and α 1 -adrenergic receptor antagonist ifenprodil on human Kv1.5 channel

Escitalopram block of hERG potassium channels

Vacuolar ion channels in the liverwort Marchantia polymorpha: influence of ion channel inhibitors

Combined transcriptomic and proteomic analysis reveals a diversity of venom-related and toxin-like peptides expressed in the mat anemone Zoanthus natalensis (Cnidaria, Hexacorallia)

Mitochondrial KATP channel involvement in angiotensin II-induced autophagy in vascular smooth muscle cells

Fampridine is a Substrate and Inhibitor of Human OCT2, but not of Human MATE1, or MATE2K

Contribution of ion currents to beat-to-beat variability of action potential duration in canine ventricular myocytes

Sustained-released fampridine in multiple sclerosis: effects on gait parameters, arm function, fatigue, and quality of life

Novel electrophysiological properties of dronedarone: inhibition of human cardiac two-pore-domain potassium (K2P) channels

Compilation and physicochemical classification analysis of a diverse hERG inhibition database

Hydrogen peroxide induces vasorelaxation by enhancing 4-aminopyridine-sensitive Kv currents through S-glutathionylation

The role of KCa3.1 channels in cardiac fibrosis induced by pressure overload in rats

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