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Discovery of a Pharmacologically Active Antagonist of the Two-Pore-Domain Potassium Channel K2P9.1 (TASK-3)

ChemMedChem, 2012-01, Vol.7 (1), p.123-133

2012

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Identification, structural, and biophysical characterization of a positive modulator of human Kv3.1 channels

Proceedings of the National Academy of Sciences - PNAS, 2023-10, Vol.120 (42), p.e2220029120-e2220029120

2023

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2‑Aminopyridines as Potent and Selective Nav1.8 Inhibitors Exhibiting Efficacy in a Nonhuman Primate Pain Model

ACS medicinal chemistry letters, 2024-06, Vol.15 (6), p.917-923

2024

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Functional TASK-3–Like Channels in Mitochondria of Aldosterone-Producing Zona Glomerulosa Cells

Hypertension (Dallas, Tex. 1979), 2017-08, Vol.70 (2), p.347-356

2017

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A Cation-π Interaction Discriminates among Sodium Channels That Are Either Sensitive or Resistant to Tetrodotoxin Block

The Journal of biological chemistry, 2007-03, Vol.282 (11), p.8044-8051

2007

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TASK-3 as a potential antidepressant target

Brain research, 2011-10, Vol.1416, p.69-79

2011

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Calcium Block of Single Sodium Channels: Role of a Pore-Lining Aromatic Residue

Biophysical journal, 2007-10, Vol.93 (7), p.2341-2349

2007

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Positive Allosteric Interaction of Structurally Diverse T-Type Calcium Channel Antagonists

Cell biochemistry and biophysics, 2009-11, Vol.55 (2), p.81-93

2009

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T-type calcium channels regulate cortical plasticity in-vivo NR-D-08-7049

Neuroreport, 2009-02, Vol.20 (3), p.257-262

2009

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T-type calcium channels regulate cortical plasticity in-vivo. [corrected]

Neuroreport, 2009-02, Vol.20 (3), p.257-262

2009

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2-Aminopyridines as Potent and Selective Na v 1.8 Inhibitors Exhibiting Efficacy in a Nonhuman Primate Pain Model

ACS medicinal chemistry letters, 2024-06, Vol.15 (6), p.917-923

2024

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A Cation-Ï Interaction Discriminates among Sodium Channels That Are Either Sensitive or Resistant to Tetrodotoxin Block

The Journal of biological chemistry, 2007-03, Vol.282 (11), p.8044

2007

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Discovery of a Pharmacologically Active Antagonist of the Two‐Pore‐Domain Potassium Channel K 2P 9.1 (TASK‐3)

ChemMedChem, 2012-01, Vol.7 (1), p.123-133

2012

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Generation and characterization of a cell line with inducible expression of Ca(v)3.2 (T-type) channels

Assay and drug development technologies, 2003-10, Vol.1 (5), p.637-645

2003

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Generation and Characterization of a Cell Line with Inducible Expression of Ca v 3.2 (T-Type) Channels

Assay and drug development technologies, 2003-10, Vol.1 (5), p.637-645

2003

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Fiber based high power low noise single frequency lasers and applications

EPJ Web of conferences, 2022, Vol.267, p.2044

2022

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Chromatographic purification of an insoluble histidine tag recombinant Ykt6p SNARE from Arabidopsis thaliana over-expressed in E. coli

Journal of chromatography. B, 2004-08, Vol.808 (1), p.83-89

2004

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Evaluation of Matrex cellufine GH 25

Journal of biochemical and biophysical methods, 2003-06, Vol.56 (1), p.69-78

2003

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Discovery of a Pharmacologically Active Antagonist of the Two-Pore-Domain Potassium Channel K2P9.1 (TASK-3)

Identification, structural, and biophysical characterization of a positive modulator of human Kv3.1 channels

2‑Aminopyridines as Potent and Selective Nav1.8 Inhibitors Exhibiting Efficacy in a Nonhuman Primate Pain Model

Functional TASK-3–Like Channels in Mitochondria of Aldosterone-Producing Zona Glomerulosa Cells

A Cation-π Interaction Discriminates among Sodium Channels That Are Either Sensitive or Resistant to Tetrodotoxin Block

TASK-3 as a potential antidepressant target

Calcium Block of Single Sodium Channels: Role of a Pore-Lining Aromatic Residue

Positive Allosteric Interaction of Structurally Diverse T-Type Calcium Channel Antagonists

T-type calcium channels regulate cortical plasticity in-vivo NR-D-08-7049

T-type calcium channels regulate cortical plasticity in-vivo. [corrected]

2-Aminopyridines as Potent and Selective Na v 1.8 Inhibitors Exhibiting Efficacy in a Nonhuman Primate Pain Model

A Cation-Ï Interaction Discriminates among Sodium Channels That Are Either Sensitive or Resistant to Tetrodotoxin Block

Discovery of a Pharmacologically Active Antagonist of the Two‐Pore‐Domain Potassium Channel K 2P 9.1 (TASK‐3)

Generation and characterization of a cell line with inducible expression of Ca(v)3.2 (T-type) channels

Generation and Characterization of a Cell Line with Inducible Expression of Ca v 3.2 (T-Type) Channels

Fiber based high power low noise single frequency lasers and applications

Chromatographic purification of an insoluble histidine tag recombinant Ykt6p SNARE from Arabidopsis thaliana over-expressed in E. coli

Evaluation of Matrex cellufine GH 25

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