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Dromedary immune response and specific Kv2.1 antibody generation using a specific immunization approach

International journal of biological macromolecules, 2016-12, Vol.93 (Pt A), p.167-171

2016

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Ultrasound modulates ion channel currents

Scientific reports, 2016-04, Vol.6 (1), p.24170-24170, Article 24170

2016

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Cobatoxin 1 from Centruroides noxius scorpion venom: chemical synthesis, three-dimensional structure in solution, pharmacology and docking on K+ channels

Biochemical journal, 2004-01, Vol.377 (Pt 1), p.37-49

2004

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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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Photochromic Blockers of Voltage-Gated Potassium Channels

Angewandte Chemie (International ed.), 2009-01, Vol.48 (48), p.9097-9101

2009

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Structural implications of hERG K+ channel block by a high-affinity minimally structured blocker

The Journal of biological chemistry, 2018-05, Vol.293 (18), p.7040-7057

2018

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Expression of the green fluorescent protein in the oligodendrocyte lineage: a transgenic mouse for developmental and physiological studies

Journal of neuroscience research, 2002-11, Vol.70 (4), p.529-545

2002

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N‐terminally extended analogues of the K+ channel toxin from Stichodactyla helianthus as potent and selective blockers of the voltage‐gated potassium channel Kv1.3

The FEBS journal, 2015-06, Vol.282 (12), p.2247-2259

2015

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Crystal Structure of the Human K2P TRAAK, a Lipid-and Mechano-Sensitive K⁺ Ion Channel

Science (American Association for the Advancement of Science), 2012-01, Vol.335 (6067), p.436-441

2012

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Human cerebral cortex development from pluripotent stem cells to functional excitatory synapses

Nature neuroscience, 2012-03, Vol.15 (3), p.477-486

2012

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An evaluation of 30 clinical drugs against the comprehensive in vitro proarrhythmia assay (CiPA) proposed ion channel panel

Journal of pharmacological and toxicological methods, 2016-09, Vol.81 (C), p.251-262

2016

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Methotrexate, a small molecular scaffold targeting Kv1.3 channel extracellular pore region

Biochemical and biophysical research communications, 2020-11, Vol.532 (2), p.265-270

2020

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Novel cell-free high-throughput screening method for pharmacological tools targeting K⁺ channels

Proceedings of the National Academy of Sciences - PNAS, 2016-05, Vol.113 (20), p.5748-5753

2016

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XE991 and Linopirdine Are State-Dependent Inhibitors for Kv7/KCNQ Channels that Favor Activated Single Subunits

The Journal of pharmacology and experimental therapeutics, 2017-07, Vol.362 (1), p.177

2017

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Role of Small-Conductance Calcium-Activated Potassium Channels in Atrial Electrophysiology and Fibrillation in the Dog

Circulation (New York, N.Y.), 2014-01, Vol.129 (4), p.430-440

2014

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Crystal Structure of the Eukaryotic Strong Inward-Rectifier K+ Channel Kir2.2 at 3.1 Å Resolution

Science (American Association for the Advancement of Science), 2009-12, Vol.326 (5960), p.1668-1674

2009

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8-hydroxypinoresinol-4-O-β-D-glucoside from Valeriana officinalis L. Is a Novel Kv1.5 Channel Blocker

Journal of ethnopharmacology, 2021-08, Vol.276, p.114168-114168, Article 114168

2021

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Large-scale mutational analysis of Kv11.1 reveals molecular insights into type 2 long QT syndrome

Nature communications, 2014-11, Vol.5 (1), p.5535-5535, Article 5535

2014

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A novel, potent, and selective inhibitor of cardiac late sodium current suppresses experimental arrhythmias

The Journal of pharmacology and experimental therapeutics, 2013-01, Vol.344 (1), p.23

2013

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A new negative allosteric modulator, AP14145, for the study of small conductance calcium‐activated potassium (KCa2) channels

British journal of pharmacology, 2017-12, Vol.174 (23), p.4396-4408

2017

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Suppression of KCNQ/M (Kv7) potassium channels in dorsal root ganglion neurons contributes to the development of bone cancer pain in a rat model

Pain (Amsterdam), 2013-03, Vol.154 (3), p.434-448

2013

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Kv2 channel regulation of action potential repolarization and firing patterns in superior cervical ganglion neurons and hippocampal CA1 pyramidal neurons

The Journal of neuroscience, 2014-04, Vol.34 (14), p.4991-5002

2014

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Glucose-mediated inhibition of calcium-activated potassium channels limits α-cell calcium influx and glucagon secretion

American journal of physiology: endocrinology and metabolism, 2019-04, Vol.316 (4), p.E646-E659

2019

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A Specific Two-pore Domain Potassium Channel Blocker Defines the Structure of the TASK-1 Open Pore

The Journal of biological chemistry, 2011-04, Vol.286 (16), p.13977-13984

2011

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A C-terminally amidated analogue of ShK is a potent and selective blocker of the voltage-gated potassium channel Kv1.3

FEBS letters, 2012-11, Vol.586 (22), p.3996-4001

2012

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1 – 25 von 5.075

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Dromedary immune response and specific Kv2.1 antibody generation using a specific immunization approach

Ultrasound modulates ion channel currents

Cobatoxin 1 from Centruroides noxius scorpion venom: chemical synthesis, three-dimensional structure in solution, pharmacology and docking on K+ channels

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

Photochromic Blockers of Voltage-Gated Potassium Channels

Structural implications of hERG K+ channel block by a high-affinity minimally structured blocker

Expression of the green fluorescent protein in the oligodendrocyte lineage: a transgenic mouse for developmental and physiological studies

N‐terminally extended analogues of the K+ channel toxin from Stichodactyla helianthus as potent and selective blockers of the voltage‐gated potassium channel Kv1.3

Crystal Structure of the Human K2P TRAAK, a Lipid-and Mechano-Sensitive K⁺ Ion Channel

Human cerebral cortex development from pluripotent stem cells to functional excitatory synapses

An evaluation of 30 clinical drugs against the comprehensive in vitro proarrhythmia assay (CiPA) proposed ion channel panel

Methotrexate, a small molecular scaffold targeting Kv1.3 channel extracellular pore region

Novel cell-free high-throughput screening method for pharmacological tools targeting K⁺ channels

XE991 and Linopirdine Are State-Dependent Inhibitors for Kv7/KCNQ Channels that Favor Activated Single Subunits

Role of Small-Conductance Calcium-Activated Potassium Channels in Atrial Electrophysiology and Fibrillation in the Dog

Crystal Structure of the Eukaryotic Strong Inward-Rectifier K+ Channel Kir2.2 at 3.1 Å Resolution

8-hydroxypinoresinol-4-O-β-D-glucoside from Valeriana officinalis L. Is a Novel Kv1.5 Channel Blocker

Large-scale mutational analysis of Kv11.1 reveals molecular insights into type 2 long QT syndrome

A novel, potent, and selective inhibitor of cardiac late sodium current suppresses experimental arrhythmias

A new negative allosteric modulator, AP14145, for the study of small conductance calcium‐activated potassium (KCa2) channels

Suppression of KCNQ/M (Kv7) potassium channels in dorsal root ganglion neurons contributes to the development of bone cancer pain in a rat model

Kv2 channel regulation of action potential repolarization and firing patterns in superior cervical ganglion neurons and hippocampal CA1 pyramidal neurons

Glucose-mediated inhibition of calcium-activated potassium channels limits α-cell calcium influx and glucagon secretion

A Specific Two-pore Domain Potassium Channel Blocker Defines the Structure of the TASK-1 Open Pore

A C-terminally amidated analogue of ShK is a potent and selective blocker of the voltage-gated potassium channel Kv1.3

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