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Constitutive, Basal, and β-Alanine-Mediated Activation of the Human Mas-Related G Protein-Coupled Receptor D Induces Release of the Inflammatory Cytokine IL-6 and Is Dependent on NF-κB Signaling

International journal of molecular sciences, 2021-12, Vol.22 (24), p.13254

2021

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Modulation of Closed-State Inactivation in Kv2.1/Kv6.4 Heterotetramers as Mechanism for 4-AP Induced Potentiation

PloS one, 2015-10, Vol.10 (10), p.e0141349-e0141349

2015

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Hydrophobic Drug/Toxin Binding Sites in Voltage-Dependent K+ and Na+ Channels

Frontiers in pharmacology, 2020-05, Vol.11, p.735-735

2020

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Being flexible: the voltage-controllable activation gate of kv channels

Frontiers in pharmacology, 2012-01, Vol.3, p.168-168

2012

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The subfamily-specific interaction between Kv2.1 and Kv6.4 subunits is determined by interactions between the N- and C-termini

PloS one, 2014-06, Vol.9 (6), p.e98960

2014

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The ladder-shaped polyether toxin gambierol anchors the gating machinery of Kv3.1 channels in the resting state

The Journal of general physiology, 2013-03, Vol.141 (3), p.359-369

2013

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Pharmacological Profile of the Sodium Current in Human Stem Cell-Derived Cardiomyocytes Compares to Heterologous Nav1.5+β1 Model

Frontiers in pharmacology, 2019, Vol.10, p.1374-1374

2019

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The electrically silent Kv6.4 subunit confers hyperpolarized gating charge movement in Kv2.1/Kv6.4 heterotetrameric channels

PloS one, 2012-05, Vol.7 (5), p.e37143-e37143

2012

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Kv channel gating requires a compatible S4-S5 linker and bottom part of S6, constrained by non-interacting residues

The Journal of general physiology, 2008-12, Vol.132 (6), p.667-680

2008

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A Polyether Biotoxin Binding Site on the Lipid-Exposed Face of the Pore Domain of KV Channels Revealed by the Marine Toxin Gambierol

Proceedings of the National Academy of Sciences - PNAS, 2009-06, Vol.106 (24), p.9896-9901

2009

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Gambierol, a toxin produced by the dinoflagellate Gambierdiscus toxicus, is a potent blocker of voltage-gated potassium channels

Toxicon (Oxford), 2008-05, Vol.51 (6), p.974-983

2008

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Kv2.1 and silent Kv subunits underlie the delayed rectifier K+ current in cultured small mouse DRG neurons

American Journal of Physiology: Cell Physiology, 2009-06, Vol.296 (6), p.C1271-C1278

2009

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Determining the correct stoichiometry of Kv2.1/Kv6.4 heterotetramers, functional in multiple stoichiometrical configurations

Proceedings of the National Academy of Sciences - PNAS, 2020-04, Vol.117 (17), p.9365-9376

2020

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Electrically silent Kv subunits: their molecular and functional characteristics

Physiology (Bethesda, Md.), 2012-04, Vol.27 (2), p.73-84

2012

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Role of the S6 C-terminus in KCNQ1 channel gating

The Journal of physiology, 2007-12, Vol.585 (2), p.325-337

2007

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REPLY TO PISUPATI ET AL: Evaluating single subunit counting data to find the correct stoichiometry

Proceedings of the National Academy of Sciences - PNAS, 2020-11, Vol.117 (47), p.29290-29291

2020

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Independent movement of the voltage sensors in KV2.1/KV6.4 heterotetramers

Scientific reports, 2017-01, Vol.7 (1), p.41646-41646, Article 41646

2017

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The Selectivity Filter Is Involved in the U-Type Inactivation Process of Kv2.1 and Kv3.1 Channels

Biophysical journal, 2020-05, Vol.118 (10), p.2612-2620

2020

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Conserved Negative Charges in the N-terminal Tetramerization Domain Mediate Efficient Assembly of Kv2.1 and Kv2.1/Kv6.4 Channels

The Journal of biological chemistry, 2009-11, Vol.284 (46), p.31625-31634

2009

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A Novel Mutation (T65P) in the PAS Domain of the Human Potassium Channel HERG Results in the Long QT Syndrome by Trafficking Deficiency

The Journal of biological chemistry, 2002-12, Vol.277 (50), p.48610-48616

2002

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Gating of Shaker-type Channels Requires the Flexibility of S6 Caused by Prolines

The Journal of biological chemistry, 2003-12, Vol.278 (50), p.50724-50731

2003

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The anticonvulsant retigabine suppresses neuronal KV2-mediated currents

Scientific reports, 2016-10, Vol.6 (1), p.35080-35080, Article 35080

2016

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Molecular mechanism for depolarization-induced modulation of Kv channel closure

The Journal of general physiology, 2012-11, Vol.140 (5), p.481-493

2012

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Domain analysis of Kv6.3, an electrically silent channel

The Journal of physiology, 2005-11, Vol.568 (3), p.737-747

2005

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Mutations in the S6 Gate Isolate a Late Step in the Activation Pathway and Reduce 4-AP Sensitivity in Shaker Kv Channel

Biophysical journal, 2014-01, Vol.106 (1), p.134-144

2014

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Constitutive, Basal, and β-Alanine-Mediated Activation of the Human Mas-Related G Protein-Coupled Receptor D Induces Release of the Inflammatory Cytokine IL-6 and Is Dependent on NF-κB Signaling

Modulation of Closed-State Inactivation in Kv2.1/Kv6.4 Heterotetramers as Mechanism for 4-AP Induced Potentiation

Hydrophobic Drug/Toxin Binding Sites in Voltage-Dependent K+ and Na+ Channels

Being flexible: the voltage-controllable activation gate of kv channels

The subfamily-specific interaction between Kv2.1 and Kv6.4 subunits is determined by interactions between the N- and C-termini

The ladder-shaped polyether toxin gambierol anchors the gating machinery of Kv3.1 channels in the resting state

Pharmacological Profile of the Sodium Current in Human Stem Cell-Derived Cardiomyocytes Compares to Heterologous Nav1.5+β1 Model

The electrically silent Kv6.4 subunit confers hyperpolarized gating charge movement in Kv2.1/Kv6.4 heterotetrameric channels

Kv channel gating requires a compatible S4-S5 linker and bottom part of S6, constrained by non-interacting residues

A Polyether Biotoxin Binding Site on the Lipid-Exposed Face of the Pore Domain of KV Channels Revealed by the Marine Toxin Gambierol

Gambierol, a toxin produced by the dinoflagellate Gambierdiscus toxicus, is a potent blocker of voltage-gated potassium channels

Kv2.1 and silent Kv subunits underlie the delayed rectifier K+ current in cultured small mouse DRG neurons

Determining the correct stoichiometry of Kv2.1/Kv6.4 heterotetramers, functional in multiple stoichiometrical configurations

Electrically silent Kv subunits: their molecular and functional characteristics

Role of the S6 C-terminus in KCNQ1 channel gating

REPLY TO PISUPATI ET AL: Evaluating single subunit counting data to find the correct stoichiometry

Independent movement of the voltage sensors in KV2.1/KV6.4 heterotetramers

The Selectivity Filter Is Involved in the U-Type Inactivation Process of Kv2.1 and Kv3.1 Channels

Conserved Negative Charges in the N-terminal Tetramerization Domain Mediate Efficient Assembly of Kv2.1 and Kv2.1/Kv6.4 Channels

A Novel Mutation (T65P) in the PAS Domain of the Human Potassium Channel HERG Results in the Long QT Syndrome by Trafficking Deficiency

Gating of Shaker-type Channels Requires the Flexibility of S6 Caused by Prolines

The anticonvulsant retigabine suppresses neuronal KV2-mediated currents

Molecular mechanism for depolarization-induced modulation of Kv channel closure

Domain analysis of Kv6.3, an electrically silent channel

Mutations in the S6 Gate Isolate a Late Step in the Activation Pathway and Reduce 4-AP Sensitivity in Shaker Kv Channel

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