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Frank E Blaney

Showing results (1-10 of 22) with videos related to

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Current Protocols in Pharmacology|February 2, 2012
Approaches to the molecular modeling of 7-transmembrane helical receptorsFrank E Blaney
Proteins|February 22, 2011
Modeling GPCR active state conformations: the β(2)-adrenergic receptorLisa M Simpson, Ian D Wall, Frank E Blaney, et al.
Journal of Medicinal Chemistry|June 23, 2009
Definition of the G protein-coupled receptor transmembrane bundle binding pocket and calculation of receptor similarities for drug designDavid E Gloriam, Steven M Foord, Frank E Blaney, et al.
Pharmacology & Therapeutics|February 25, 2014
Unifying family A GPCR theories of activationBenjamin G Tehan, Andrea Bortolato, Frank E Blaney, et al.
Methods in Enzymology|February 5, 2013
Modeling active GPCR conformationsBruck Taddese, Lisa M Simpson, Ian D Wall, et al.
Biochemistry|March 17, 2004
Evidence for the proximity of the extreme N-terminus of the neurokinin-2 (NK2) tachykinin receptor to Cys167 in the putative fourth transmembrane helixNirmala Bhogal, Frank E Blaney, Paul M Ingley, et al.
The Journal of Biological Chemistry|February 24, 2009
Structural determinants of drugs acting on the Nav1.8 channelLiam E Browne, Frank E Blaney, Shahnaz P Yusaf, et al.
Molecular Pharmacology|November 29, 2007
2-[2-(3,4-dichloro-phenyl)-2,3-dihydro-1H-isoindol-5-ylamino]-nicotinic acid (PD-307243) causes instantaneous current through human ether-a-go-go-related gene potassium channelsEarl Gordon, Irina M Lozinskaya, Zuojun Lin, et al.
Molecular Pharmacology|December 4, 2003
Differences in the central nervous system distribution and pharmacology of the mouse 5-hydroxytryptamine-6 receptor compared with rat and human receptors investigated by radioligand binding, site-directed mutagenesis, and molecular modelingWarren D Hirst, Bjarke Abrahamsen, Frank E Blaney, et al.
Journal of Molecular Modeling|March 2, 2006
Modeling the pore structure of voltage-gated sodium channels in closed, open, and fast-inactivated conformation reveals details of site 1 toxin and local anesthetic bindingHolger Scheib, Iain McLay, Nicolas Guex, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Current Protocols in Pharmacology|February 2, 2012
Approaches to the molecular modeling of 7-transmembrane helical receptorsFrank E Blaney
Proteins|February 22, 2011
Modeling GPCR active state conformations: the β(2)-adrenergic receptorLisa M Simpson, Ian D Wall, Frank E Blaney, et al.
Journal of Medicinal Chemistry|June 23, 2009
Definition of the G protein-coupled receptor transmembrane bundle binding pocket and calculation of receptor similarities for drug designDavid E Gloriam, Steven M Foord, Frank E Blaney, et al.
Pharmacology & Therapeutics|February 25, 2014
Unifying family A GPCR theories of activationBenjamin G Tehan, Andrea Bortolato, Frank E Blaney, et al.
Methods in Enzymology|February 5, 2013
Modeling active GPCR conformationsBruck Taddese, Lisa M Simpson, Ian D Wall, et al.
Biochemistry|March 17, 2004
Evidence for the proximity of the extreme N-terminus of the neurokinin-2 (NK2) tachykinin receptor to Cys167 in the putative fourth transmembrane helixNirmala Bhogal, Frank E Blaney, Paul M Ingley, et al.
The Journal of Biological Chemistry|February 24, 2009
Structural determinants of drugs acting on the Nav1.8 channelLiam E Browne, Frank E Blaney, Shahnaz P Yusaf, et al.
Molecular Pharmacology|November 29, 2007
2-[2-(3,4-dichloro-phenyl)-2,3-dihydro-1H-isoindol-5-ylamino]-nicotinic acid (PD-307243) causes instantaneous current through human ether-a-go-go-related gene potassium channelsEarl Gordon, Irina M Lozinskaya, Zuojun Lin, et al.
Molecular Pharmacology|December 4, 2003
Differences in the central nervous system distribution and pharmacology of the mouse 5-hydroxytryptamine-6 receptor compared with rat and human receptors investigated by radioligand binding, site-directed mutagenesis, and molecular modelingWarren D Hirst, Bjarke Abrahamsen, Frank E Blaney, et al.
Journal of Molecular Modeling|March 2, 2006
Modeling the pore structure of voltage-gated sodium channels in closed, open, and fast-inactivated conformation reveals details of site 1 toxin and local anesthetic bindingHolger Scheib, Iain McLay, Nicolas Guex, et al.
Pageof 3