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Circulation Research|September 23, 2003
Antiarrhythmic drug target choices and screeningMichael C Sanguinetti, Paul B BennettCurrent Opinion in Pharmacology|April 12, 2014
HERG1 channel agonists and cardiac arrhythmiaMichael C SanguinettiPflugers Archiv : European Journal of Physiology|June 15, 2010
HERG1 channelopathiesMichael C SanguinettiMolecular Pharmacology|February 17, 2009
Niflumic acid alters gating of HCN2 pacemaker channels by interaction with the outer region of S4 voltage sensing domainsLan Cheng, Michael C SanguinettiAdvances in Experimental Medicine and Biology|February 9, 2022
Physiological Functions, Biophysical Properties, and Regulation of KCNQ1 (KV7.1) Potassium ChannelsMichael C Sanguinetti, Guiscard SeebohmCardiac Electrophysiology Clinics|June 5, 2016
Molecular Basis of Cardiac Delayed Rectifier Potassium Channel Function and PharmacologyWei Wu, Michael C SanguinettiMolecular Pharmacology|December 29, 2007
A single amino acid difference between ether-a-go-go- related gene channel subtypes determines differential sensitivity to a small molecule activatorMatthew Perry, Michael C SanguinettiPhysiological Reports|September 13, 2014
Intracellular ATP does not inhibit Slo2.1 K+ channelsPriyanka Garg, Michael C SanguinettiMolecular Pharmacology|April 19, 2015
C-Linker Accounts for Differential Sensitivity of ERG1 and ERG2 K+ Channels to RPR260243-Induced Slow DeactivationAlison Gardner, Michael C SanguinettiMolecular Pharmacology|August 2, 2012
Structure-activity relationship of fenamates as Slo2.1 channel activatorsPriyanka Garg, Michael C SanguinettiPageof 9