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Cellular elements for seeing in the dark: voltage-dependent conductances in cockroach photoreceptors

BMC neuroscience, 2012-08, Vol.13 (1), p.93-93, Article 93

2012

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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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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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Thallium-sensitive fluorescent assay reveals loperamide as a new inhibitor of the potassium channel Kv10.1

Pharmacological reports, 2021-12, Vol.73 (6), p.1744-1753

2021

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Why are most phospholipidosis inducers also hERG blockers?

Archives of toxicology, 2017-12, Vol.91 (12), p.3885-3895

2017

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Atypical antipsychotic olanzapine inhibits voltage-dependent K+ channels in coronary arterial smooth muscle cells

Pharmacological reports, 2021-12, Vol.73 (6), p.1724-1733

2021

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The impact of hyperpolarization-activated cyclic nucleotide-gated (HCN) and voltage-gated potassium KCNQ/Kv7 channels on primary microglia function

Journal of neuroinflammation, 2020-04, Vol.17 (1), p.100-100, Article 100

2020

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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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Repurposing the K Ca 3.1 Blocker Senicapoc for Ischemic Stroke

Translational stroke research, 2024-06, Vol.15 (3), p.518

2024

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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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Tumor-associated macrophage-derived IL-6 and IL-8 enhance invasive activity of LoVo cells induced by PRL-3 in a KCNN4 channel-dependent manner

BMC cancer, 2014-05, Vol.14 (1), p.330-330, Article 330

2014

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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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KCNQ2/3/5 channels in dorsal root ganglion neurons can be therapeutic targets of neuropathic pain in diabetic rats

Molecular pain, 2018-01, Vol.14, p.1744806918793229

2018

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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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The Kv1.3 K+ channel in the immune system and its “precision pharmacology” using peptide toxins

Biologia futura, 2021-03, Vol.72 (1), p.75-83

2021

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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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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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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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Phytochemicals genistein and capsaicin modulate Kv2.1 channel gating

Pharmacological reports, 2017-12, Vol.69 (6), p.1145-1153

2017

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In vitro evidence that endothelium-dependent vasodilatation induced by clozapine is mediated by an ATP-sensitive potassium channel

Pharmacological reports, 2019-06, Vol.71 (3), p.522-527

2019

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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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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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Ability of naringenin, a bioflavonoid, to activate M-type potassium current in motor neuron-like cells and to increase BKCa-channel activity in HEK293T cells transfected with α-hSlo subunit

BMC neuroscience, 2014-12, Vol.15 (1), p.135-135, Article 135

2014

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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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1 – 25 von 4.642

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Cellular elements for seeing in the dark: voltage-dependent conductances in cockroach photoreceptors

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

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

Thallium-sensitive fluorescent assay reveals loperamide as a new inhibitor of the potassium channel Kv10.1

Why are most phospholipidosis inducers also hERG blockers?

Atypical antipsychotic olanzapine inhibits voltage-dependent K+ channels in coronary arterial smooth muscle cells

The impact of hyperpolarization-activated cyclic nucleotide-gated (HCN) and voltage-gated potassium KCNQ/Kv7 channels on primary microglia function

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

Repurposing the K Ca 3.1 Blocker Senicapoc for Ischemic Stroke

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

Tumor-associated macrophage-derived IL-6 and IL-8 enhance invasive activity of LoVo cells induced by PRL-3 in a KCNN4 channel-dependent manner

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

KCNQ2/3/5 channels in dorsal root ganglion neurons can be therapeutic targets of neuropathic pain in diabetic rats

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

The Kv1.3 K+ channel in the immune system and its “precision pharmacology” using peptide toxins

Escitalopram block of hERG potassium channels

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

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

Phytochemicals genistein and capsaicin modulate Kv2.1 channel gating

In vitro evidence that endothelium-dependent vasodilatation induced by clozapine is mediated by an ATP-sensitive potassium channel

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

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

Ability of naringenin, a bioflavonoid, to activate M-type potassium current in motor neuron-like cells and to increase BKCa-channel activity in HEK293T cells transfected with α-hSlo subunit

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

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