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John Dunlop

Showing results (41-50 of 99) with videos related to

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Neuropharmacology|April 26, 2016
Compromising KCC2 transporter activity enhances the development of continuous seizure activityMatthew R Kelley, Tarek Z Deeb, Nicholas J Brandon, et al.
The Journal of Pharmacology and Experimental Therapeutics|April 19, 2002
The role of transmembrane helix 5 in agonist binding to the human H3 receptorAlbert J Uveges, Dianne Kowal, Yingxin Zhang, et al.
Biochemical Pharmacology|August 21, 2007
In vitro screening strategies for nicotinic receptor ligandsJohn Dunlop, Renza Roncarati, Brian Jow, et al.
British Journal of Pharmacology|October 1, 2003
WAY-855 (3-amino-tricyclo[2.2.1.02.6]heptane-1,3-dicarboxylic acid): a novel, EAAT2-preferring, nonsubstrate inhibitor of high-affinity glutamate uptakeJohn Dunlop, Scott Eliasof, Gary Stack, et al.
Journal of Biomolecular Screening|December 19, 2007
Validation of a medium-throughput electrophysiological assay for KCNQ2/3 channel enhancers using IonWorks HTFlora Jow, Ru Shen, Pranab Chanda, et al.
European Journal of Pharmacology|July 16, 2003
Characterization of the 5-HT6 receptor coupled to Ca2+ signaling using an enabling chimeric G-proteinJean Y Zhang, Stanley Nawoschik, Dianne Kowal, et al.
Journal of Neuroscience Methods|May 11, 2007
Screening of immunophilin ligands by quantitative analysis of neurofilament expression and neurite outgrowth in cultured neurons and cellsDanni Liu, H Beal McIlvain, Myles Fennell, et al.
Assay and Drug Development Technologies|May 13, 2008
Functional properties of alpha7 nicotinic acetylcholine receptors co-expressed with RIC-3 in a stable recombinant CHO-K1 cell lineRenza Roncarati, Tamara Seredenina, Brian Jow, et al.
Journal of Neurochemistry|February 6, 2014
Inhibition of glucosylceramide synthase stimulates autophagy flux in neuronsWei Shen, Anastasia G Henry, Katrina L Paumier, et al.
Bioorganic & Medicinal Chemistry Letters|September 17, 2005
Synthesis and biological activities of aryl-ether-, biaryl-, and fluorene-aspartic acid and diaminopropionic acid analogs as potent inhibitors of the high-affinity glutamate transporter EAAT-2Alexander Greenfield, Cristina Grosanu, John Dunlop, et al.
Pageof 10

Showing results (41-50 of 99) with videos related to

Sort By:
Pageof 10
Neuropharmacology|April 26, 2016
Compromising KCC2 transporter activity enhances the development of continuous seizure activityMatthew R Kelley, Tarek Z Deeb, Nicholas J Brandon, et al.
The Journal of Pharmacology and Experimental Therapeutics|April 19, 2002
The role of transmembrane helix 5 in agonist binding to the human H3 receptorAlbert J Uveges, Dianne Kowal, Yingxin Zhang, et al.
Biochemical Pharmacology|August 21, 2007
In vitro screening strategies for nicotinic receptor ligandsJohn Dunlop, Renza Roncarati, Brian Jow, et al.
British Journal of Pharmacology|October 1, 2003
WAY-855 (3-amino-tricyclo[2.2.1.02.6]heptane-1,3-dicarboxylic acid): a novel, EAAT2-preferring, nonsubstrate inhibitor of high-affinity glutamate uptakeJohn Dunlop, Scott Eliasof, Gary Stack, et al.
Journal of Biomolecular Screening|December 19, 2007
Validation of a medium-throughput electrophysiological assay for KCNQ2/3 channel enhancers using IonWorks HTFlora Jow, Ru Shen, Pranab Chanda, et al.
European Journal of Pharmacology|July 16, 2003
Characterization of the 5-HT6 receptor coupled to Ca2+ signaling using an enabling chimeric G-proteinJean Y Zhang, Stanley Nawoschik, Dianne Kowal, et al.
Journal of Neuroscience Methods|May 11, 2007
Screening of immunophilin ligands by quantitative analysis of neurofilament expression and neurite outgrowth in cultured neurons and cellsDanni Liu, H Beal McIlvain, Myles Fennell, et al.
Assay and Drug Development Technologies|May 13, 2008
Functional properties of alpha7 nicotinic acetylcholine receptors co-expressed with RIC-3 in a stable recombinant CHO-K1 cell lineRenza Roncarati, Tamara Seredenina, Brian Jow, et al.
Journal of Neurochemistry|February 6, 2014
Inhibition of glucosylceramide synthase stimulates autophagy flux in neuronsWei Shen, Anastasia G Henry, Katrina L Paumier, et al.
Bioorganic & Medicinal Chemistry Letters|September 17, 2005
Synthesis and biological activities of aryl-ether-, biaryl-, and fluorene-aspartic acid and diaminopropionic acid analogs as potent inhibitors of the high-affinity glutamate transporter EAAT-2Alexander Greenfield, Cristina Grosanu, John Dunlop, et al.
Pageof 10