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Observation of σ-pore currents in mutant hKv1.2_V370C potassium channels

PloS one, 2017-04, Vol.12 (4), p.e0176078-e0176078

2017

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International Union of Basic and Clinical Pharmacology. C. Nomenclature and Properties of Calcium-Activated and Sodium-Activated Potassium Channels

Pharmacological reviews, 2017-01, Vol.69 (1), p.1-11

2017

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Characterization of the σ-Pore in Mutant hKv1.3 Potassium Channels

Cellular physiology and biochemistry, 2018, Vol.46 (3), p.1112-1121

2018

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International Union of Pharmacology. LIII. Nomenclature and molecular relationships of voltage-gated potassium channels

Pharmacological reviews, 2005-12, Vol.57 (4), p.473-508

2005

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International Union of Pharmacology. LII. Nomenclature and molecular relationships of calcium-activated potassium channels

Pharmacological reviews, 2005-12, Vol.57 (4), p.463-472

2005

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Kinetic Aspects of Verapamil Binding (On-Rate) on Wild-Type and Six hKv1.3 Mutant Channels

Cellular physiology and biochemistry, 2017, Vol.44 (1), p.172-184

2017

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A Novel Current Pathway Parallel to the Central Pore in a Mutant Voltage-gated Potassium Channel

The Journal of biological chemistry, 2011-06, Vol.286 (22), p.20031-20042

2011

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Blockage of Intermediate-Conductance Ca2+-Activated K+ Channels Inhibit Human Pancreatic Cancer Cell Growth in Vitro

Molecular pharmacology, 2004-03, Vol.65 (3), p.630-638

2004

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Design of a Potent and Selective Inhibitor of the Intermediate-Conductance Ca2+-Activated K+Channel, IKCa1: A Potential Immunosuppressant

Proceedings of the National Academy of Sciences - PNAS, 2000-07, Vol.97 (14), p.8151-8156

2000

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Kinetic Aspects of Verapamil Binding (On-Rate) on Wild-Type and Six h K v 1.3 Mutant Channels

Cellular physiology and biochemistry, 2018-01, Vol.44 (1), p.172-184

Grissmer, Stephan

2018

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Kv1.3-Blocking 5-Phenylalkoxypsoralens: A New Class of Immunomodulators

Molecular pharmacology, 2004-06, Vol.65 (6), p.1364-1374

2004

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Inhibitors of potassium channels Kv1.3 and IK-1 as immunosuppressants

Bioorganic & medicinal chemistry letters, 2009-04, Vol.19 (8), p.2299-2304

2009

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Chloride Influx Provokes Lamellipodium Formation in Microglial Cells

Cellular physiology and biochemistry, 2008, Vol.21 (1-3), p.55-62

2008

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Mapping of Maurotoxin Binding Sites on hKv1.2, hKv1.3, and hIKCa1 Channels

Molecular pharmacology, 2004-11, Vol.66 (5), p.1103-1112

2004

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cAMP-Dependent Chloride Conductance Evokes Ammonia-Induced Blebbing in the Microglial Cell Line, BV-2

Cellular physiology and biochemistry, 2009, Vol.24 (1-2), p.53-64

2009

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Formation of cellular projections in neural progenitor cells depends on SK3 channel activity

Journal of neurochemistry, 2007-06, Vol.101 (5), p.1338-1350

2007

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THE CONCISE GUIDE TO PHARMACOLOGY 2019/20: Ion channels

British journal of pharmacology, 2019-12, Vol.176 (S1), p.S142-S228

2019

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Evidence for the Interaction of Endophilin A3 with Endogenous Kca2.3 Channels in PC12 Cells

Cellular physiology and biochemistry, 2014, Vol.34 (2), p.474-490

2014

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Investigation of the Phenylalkylamine Binding Site in hKv1.3 (H399T), a Mutant with a Reduced C-Type Inactivated State

Molecular pharmacology, 2005-10, Vol.68 (4), p.966

2005

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Effect of 2-Aminoethylmethanethiosulphonate (MTSEA) on the HKV1.3_L346C and the HKV1.3_L346C_L418C Mutant Channels

Biophysical journal, 2016-02, Vol.110 (3), p.278a-278a

2016

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Characterization of the σ-Pore in Mutant hKv1.3 Potassium Channels

Biophysical journal, 2016-02, Vol.110 (3), p.277a-277a

2016

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Evidence for the Interaction of Endophilin 3 with the SK3 Channels in PC12 Cells

Biophysical journal, 2014-01, Vol.106 (2), p.748a-749a

2014

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THE CONCISE GUIDE TO PHARMACOLOGY 2021/22: Ion channels

British journal of pharmacology, 2021-10, Vol.178 (S1), p.S157-S245

2021

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Pharmacological Profiling of Orthochirus scrobiculosus Toxin 1 Analogs with a Trimmed N-Terminal Domain

Molecular pharmacology, 2006-01, Vol.69 (1), p.354-362

2006

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Interaction of d-Tubocurarine with Potassium Channels: Molecular Modeling and Ligand Binding

Molecular pharmacology, 2006-04, Vol.69 (4), p.1356-1365

2006

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Observation of σ-pore currents in mutant hKv1.2_V370C potassium channels

International Union of Basic and Clinical Pharmacology. C. Nomenclature and Properties of Calcium-Activated and Sodium-Activated Potassium Channels

Characterization of the σ-Pore in Mutant hKv1.3 Potassium Channels

International Union of Pharmacology. LIII. Nomenclature and molecular relationships of voltage-gated potassium channels

International Union of Pharmacology. LII. Nomenclature and molecular relationships of calcium-activated potassium channels

Kinetic Aspects of Verapamil Binding (On-Rate) on Wild-Type and Six hKv1.3 Mutant Channels

A Novel Current Pathway Parallel to the Central Pore in a Mutant Voltage-gated Potassium Channel

Blockage of Intermediate-Conductance Ca2+-Activated K+ Channels Inhibit Human Pancreatic Cancer Cell Growth in Vitro

Design of a Potent and Selective Inhibitor of the Intermediate-Conductance Ca2+-Activated K+Channel, IKCa1: A Potential Immunosuppressant

Kinetic Aspects of Verapamil Binding (On-Rate) on Wild-Type and Six h K v 1.3 Mutant Channels

Kv1.3-Blocking 5-Phenylalkoxypsoralens: A New Class of Immunomodulators

Inhibitors of potassium channels Kv1.3 and IK-1 as immunosuppressants

Chloride Influx Provokes Lamellipodium Formation in Microglial Cells

Mapping of Maurotoxin Binding Sites on hKv1.2, hKv1.3, and hIKCa1 Channels

cAMP-Dependent Chloride Conductance Evokes Ammonia-Induced Blebbing in the Microglial Cell Line, BV-2

Formation of cellular projections in neural progenitor cells depends on SK3 channel activity

THE CONCISE GUIDE TO PHARMACOLOGY 2019/20: Ion channels

Evidence for the Interaction of Endophilin A3 with Endogenous Kca2.3 Channels in PC12 Cells

Investigation of the Phenylalkylamine Binding Site in hKv1.3 (H399T), a Mutant with a Reduced C-Type Inactivated State

Effect of 2-Aminoethylmethanethiosulphonate (MTSEA) on the HKV1.3_L346C and the HKV1.3_L346C_L418C Mutant Channels

Characterization of the σ-Pore in Mutant hKv1.3 Potassium Channels

Evidence for the Interaction of Endophilin 3 with the SK3 Channels in PC12 Cells

THE CONCISE GUIDE TO PHARMACOLOGY 2021/22: Ion channels

Pharmacological Profiling of Orthochirus scrobiculosus Toxin 1 Analogs with a Trimmed N-Terminal Domain

Interaction of d-Tubocurarine with Potassium Channels: Molecular Modeling and Ligand Binding

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