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In silico models of the macromolecular NaV1.5-KIR2.1 complex

Frontiers in physiology, 2024-02, Vol.15, p.1362964-1362964

Stary-Weinzinger, Anna

2024

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Histidine at position 462 determines the low quinine sensitivity of ether‐à‐go‐go channel superfamily member Kv12.1

British journal of pharmacology, 2019-08, Vol.176 (15), p.2708-2723

2019

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LUF7244, an allosteric modulator/activator of Kv11.1 channels, counteracts dofetilide‐induced torsades de pointes arrhythmia in the chronic atrioventricular block dog model

British journal of pharmacology, 2019-10, Vol.176 (19), p.3871-3885

2019

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Glibenclamide and HMR1098 normalize Cantú syndrome‐associated gain‐of‐function currents

Journal of cellular and molecular medicine, 2019-08, Vol.23 (8), p.4962-4969

2019

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A structural model of the human serotonin transporter in an outward-occluded state

PloS one, 2019-06, Vol.14 (6), p.e0217377

2019

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Subunit gating resulting from individual protonation events in Kir2 channels

Nature communications, 2023-07, Vol.14 (1), p.4538-4538, Article 4538

2023

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Computational Insights Into Voltage Dependence of Polyamine Block in a Strong Inwardly Rectifying K + Channel

Frontiers in pharmacology, 2020-05, Vol.11, p.721

2020

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Different inward and outward conduction mechanisms in NaVMs suggested by molecular dynamics simulations

PLoS computational biology, 2014-07, Vol.10 (7), p.e1003746

2014

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Simulating PIP2-Induced Gating Transitions in Kir6.2 Channels

Frontiers in molecular biosciences, 2021-08, Vol.8

2021

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A selectivity filter mutation provides insights into gating regulation of a K+ channel

Communications biology, 2022-04, Vol.5 (1), p.345-345, Article 345

2022

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The Bradycardic Agent Ivabradine Acts as an Atypical Inhibitor of Voltage-Gated Sodium Channels

Frontiers in pharmacology, 2022-05, Vol.13, p.809802-809802

2022

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Molecular Insights into hERG Potassium Channel Blockade by Lubeluzole

Cellular physiology and biochemistry, 2018-04, Vol.45 (6), p.2233-2245

2018

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Development of new K ir 2.1 channel openers from propafenone analogues

British journal of pharmacology, 2024-10

2024

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Probing the energy landscape of activation gating of the bacterial potassium channel KcsA

PLoS computational biology, 2013-05, Vol.9 (5), p.e1003058

2013

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Toward a Consensus Model of the hERG Potassium Channel

ChemMedChem, 2010-03, Vol.5 (3), p.455-467

2010

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Development of IKATP Ion Channel Blockers Targeting Sulfonylurea Resistant Mutant KIR6.2 Based Channels for Treating DEND Syndrome

Frontiers in pharmacology, 2022-01, Vol.12, p.814066-814066

2022

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Binding of RPR260243 at the intracellular side of the hERG1 channel pore domain slows closure of the helix bundle crossing gate

Frontiers in molecular biosciences, 2023-02, Vol.10, p.1137368-1137368

2023

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Coupled and Independent Contributions of Residues in IS6 and IIS6 to Activation Gating of CaV1.2

The Journal of biological chemistry, 2009-05, Vol.284 (18), p.12276-12284

2009

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In silico analysis of conformational changes induced by mutation of aromatic binding residues: consequences for drug binding in the hERG K+ channel

PloS one, 2011-12, Vol.6 (12), p.e28778-e28778

2011

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Disease Associated Mutations in KIR Proteins Linked to Aberrant Inward Rectifier Channel Trafficking

Biomolecules (Basel, Switzerland), 2019-10, Vol.9 (11), p.650

2019

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Histidine at position 462 determines the low quinine sensitivity of ether-à-go-go channel superfamily member K v 12.1

British journal of pharmacology, 2019-08, Vol.176 (15), p.2708-2723

2019

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Computational Identification of Novel Kir6 Channel Inhibitors

Frontiers in pharmacology, 2019-05, Vol.10, p.549

2019

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β subunits of GABAA receptors form proton-gated chloride channels: Insights into the molecular basis

Communications biology, 2022-08, Vol.5 (1), p.784-10, Article 784

2022

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PA-6 inhibits inward rectifier currents carried by V93I and D172N gain-of-function KIR2.1 channels, but increases channel protein expression

Journal of biomedical science, 2017-07, Vol.24 (1), p.1-10, Article 44

2017

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Allosteric gating mechanisms of inward rectifying K+ channel 3.2 guided by disease mutations

Biophysical journal, 2024-02, Vol.123 (3), p.255a-255a

2024

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In silico models of the macromolecular NaV1.5-KIR2.1 complex

Histidine at position 462 determines the low quinine sensitivity of ether‐à‐go‐go channel superfamily member Kv12.1

LUF7244, an allosteric modulator/activator of Kv11.1 channels, counteracts dofetilide‐induced torsades de pointes arrhythmia in the chronic atrioventricular block dog model

Glibenclamide and HMR1098 normalize Cantú syndrome‐associated gain‐of‐function currents

A structural model of the human serotonin transporter in an outward-occluded state

Subunit gating resulting from individual protonation events in Kir2 channels

Computational Insights Into Voltage Dependence of Polyamine Block in a Strong Inwardly Rectifying K + Channel

Different inward and outward conduction mechanisms in NaVMs suggested by molecular dynamics simulations

Simulating PIP2-Induced Gating Transitions in Kir6.2 Channels

A selectivity filter mutation provides insights into gating regulation of a K+ channel

The Bradycardic Agent Ivabradine Acts as an Atypical Inhibitor of Voltage-Gated Sodium Channels

Molecular Insights into hERG Potassium Channel Blockade by Lubeluzole

Development of new K ir 2.1 channel openers from propafenone analogues

Probing the energy landscape of activation gating of the bacterial potassium channel KcsA

Toward a Consensus Model of the hERG Potassium Channel

Development of IKATP Ion Channel Blockers Targeting Sulfonylurea Resistant Mutant KIR6.2 Based Channels for Treating DEND Syndrome

Binding of RPR260243 at the intracellular side of the hERG1 channel pore domain slows closure of the helix bundle crossing gate

Coupled and Independent Contributions of Residues in IS6 and IIS6 to Activation Gating of CaV1.2

In silico analysis of conformational changes induced by mutation of aromatic binding residues: consequences for drug binding in the hERG K+ channel

Disease Associated Mutations in KIR Proteins Linked to Aberrant Inward Rectifier Channel Trafficking

Histidine at position 462 determines the low quinine sensitivity of ether-à-go-go channel superfamily member K v 12.1

Computational Identification of Novel Kir6 Channel Inhibitors

β subunits of GABAA receptors form proton-gated chloride channels: Insights into the molecular basis

PA-6 inhibits inward rectifier currents carried by V93I and D172N gain-of-function KIR2.1 channels, but increases channel protein expression

Allosteric gating mechanisms of inward rectifying K+ channel 3.2 guided by disease mutations

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