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The Journal of Pharmacology and Experimental Therapeutics|October 26, 2007
[3H]A-585539 [(1S,4S)-2,2-dimethyl-5-(6-phenylpyridazin-3-yl)-5-aza-2-azoniabicyclo[2.2.1]heptane], a novel high-affinity alpha7 neuronal nicotinic receptor agonist: radioligand binding characterization to rat and human brainDavid J Anderson, William Bunnelle, Bruce Surber, et al.
Bioorganic & Medicinal Chemistry Letters|December 4, 2009
Structure-activity relationships of N-substituted ligands for the alpha7 nicotinic acetylcholine receptorKathleen H Mortell, Michael R Schrimpf, William H Bunnelle, et al.
European Journal of Pharmacology|January 20, 2004
Characterization of human urinary bladder KATP channels containing SUR2B splice variants expressed in L-cellsVictoria E Scott, Rachel A Davis-Taber, Christopher Silvia, et al.
Biochemical Pharmacology|June 27, 2009
Stimulation of dopamine release by nicotinic acetylcholine receptor ligands in rat brain slices correlates with the profile of high, but not low, sensitivity alpha4beta2 subunit combinationDavid J Anderson, John Malysz, Jens Halvard Grønlien, et al.
The Journal of Pharmacology and Experimental Therapeutics|February 28, 2002
Functional characterization of adenosine receptors and coupling to ATP-sensitive K+ channels in Guinea pig urinary bladder smooth muscleSujatha M Gopalakrishnan, Steven A Buckner, Ivan Milicic, et al.
Assay and Drug Development Technologies|April 20, 2004
Functional analysis of large conductance Ca2(+)-activated K(+) channels: ion flux studies by atomic absorption spectrometryAshutosh S Parihar, Duncan R Groebe, Victoria E Scott, et al.
Assay and Drug Development Technologies|February 12, 2011
Functional characterization and high-throughput screening of positive allosteric modulators of α7 nicotinic acetylcholine receptors in IMR-32 neuroblastoma cellsSujatha M Gopalakrishnan, Betsy M Philip, Jens Halvard Gronlien, et al.
Neuroscience Research|January 1, 2008
Analysis of gene expression profiles in rat hippocampus following treatment with nicotine and an alpha7 nAChR selective agonistJeffrey F Waring, Stephen Abel, Jinhe Li, et al.
The Journal of Biological Chemistry|June 3, 2006
Association of Catsper1 or -2 with Ca(v)3.3 leads to suppression of T-type calcium channel activityDi Zhang, Jun Chen, Anita Saraf, et al.
The Journal of Pharmacology and Experimental Therapeutics|September 18, 2002
(-)-(9S)-9-(3-Bromo-4-fluorophenyl)-2,3,5,6,7,9-hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-dioxide (A-278637): a novel ATP-sensitive potassium channel opener efficacious in suppressing urinary bladder contractions. II. in vivo characterizationMichael E Brune, Thomas A Fey, Jorge D Brioni, et al.
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