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Frontiers in Pharmacology|November 5, 2011
The sodium channel as a target for local anesthetic drugsHarry A Fozzard, Michael F Sheets, Dorothy A HanckProceedings of the National Academy of Sciences of the United States of America|September 26, 1995
A structural motif for the voltage-gated potassium channel poreG M Lipkind, D A Hanck, H A FozzardToxicon : Official Journal of the International Society on Toxinology|July 6, 2010
Inhibition of the activation pathway of the T-type calcium channel Ca(V)3.1 by ProTxIIGabrielle B Edgerton, Kenneth M Blumenthal, Dorothy A HanckBiophysical Journal|December 5, 2015
Important Role of Asparagines in Coupling the Pore and Votage-Sensor Domain in Voltage-Gated Sodium ChannelsMichael F Sheets, Harry A Fozzard, Dorothy A HanckMolecular Pharmacology|May 16, 2006
State-dependent verapamil block of the cloned human Ca(v)3.1 T-type Ca(2+) channelBenjamin S Freeze, Megan M McNulty, Dorothy A HanckPflugers Archiv : European Journal of Physiology|April 28, 2000
Lidocaine alters activation gating of cardiac Na channelsD A Hanck, J C Makielski, M F SheetsThe Journal of General Physiology|April 25, 2000
The role of the putative inactivation lid in sodium channel gating current immobilizationM F Sheets, J W Kyle, D A HanckThe Journal of General Physiology|February 2, 1999
Augmentation of recovery from inactivation by site-3 Na channel toxins. A single-channel and whole-cell study of persistent currentsG Richard Benzinger, G S Tonkovich, D A HanckCanadian Journal of Physiology and Pharmacology|July 1, 1988
The Anrep effect: an intrinsic myocardial mechanismC G Nichols, D A Hanck, B R JewellJournal of the American Chemical Society|March 7, 2002
Structures of protein-protein complexes are docked using only NMR restraints from residual dipolar coupling and chemical shift perturbationsMark A McCoy, Daniel F WyssPageof 17