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Combinatorial Chemistry & High Throughput Screening|January 20, 2009
HCN channels as targets for drug discoveryMichael P Maher, Nyan-Tsz Wu, Hong-Qing Guo, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 2, 2003
Stoichiometry of expressed KCNQ2/KCNQ3 potassium channels and subunit composition of native ganglionic M channels deduced from block by tetraethylammoniumJennifer K Hadley, Gayle M Passmore, Lucine Tatulian, et al.
American Journal of Physiology. Cell Physiology|August 2, 2003
Distribution and functional properties of human KCNH8 (Elk1) potassium channelsAnruo Zou, Zhixin Lin, Margaret Humble, et al.
Molecular Pharmacology|January 4, 2008
Activation of TRPA1 by farnesyl thiosalicylic acidMichael Maher, Hong Ao, Tue Banke, et al.
Molecular Pharmacology|March 10, 2021
The Negative Allosteric Modulator EU1794-4 Reduces Single-Channel Conductance and Ca2+ Permeability of GluN1/GluN2A N-Methyl-d-Aspartate ReceptorsRiley E Perszyk, Zhaoshi Zheng, Tue G Banke, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
N-Pyridyl and Pyrimidine Benzamides as KCNQ2/Q3 Potassium Channel Openers for the Treatment of EpilepsyGeorge Amato, Rosemarie Roeloffs, Greg C Rigdon, et al.
The Journal of Pharmacology and Experimental Therapeutics|June 26, 2008
In vivo profile of ICA-27243 [N-(6-chloro-pyridin-3-yl)-3,4-difluoro-benzamide], a potent and selective KCNQ2/Q3 (Kv7.2/Kv7.3) activator in rodent anticonvulsant modelsRosemarie Roeloffs, Alan D Wickenden, Christopher Crean, et al.
The Journal of Clinical Investigation|October 19, 2020
Functional α6β4 acetylcholine receptor expression enables pharmacological testing of nicotinic agonists with analgesic propertiesDaniel Knowland, Shenyan Gu, William A Eckert, et al.
Circulation|April 17, 2002
Inhibition of calcineurin and sarcolemmal Ca2+ influx protects cardiac morphology and ventricular function in K(v)4.2N transgenic miceRajan Sah, Gavin Y Oudit, The-Tin T Nguyen, et al.
Biorxiv : the Preprint Server for Biology|November 22, 2024
Selective Enhancement of the Interneuron Network and Gamma-Band Power via GluN2C/GluN2D NMDA Receptor PotentiationChad R Camp, Tue G Banke, Hao Xing, et al.
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