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Jules C Hancox

Showing results (171-180 of 221) with videos related to

Pageof 23
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Interface Focus|December 18, 2023
Evaluating pro-arrhythmogenic effects of the T634S-hERG mutation: insights from a simulation studyWei Hu, Wenfeng Zhang, Kevin Zhang, et al.
Molecular Pharmacology|August 24, 2004
Evidence for a novel K(+) channel modulated by alpha(1A)-adrenoceptors in cardiac myocytesStéphanie C M Choisy, Jules C Hancox, Lesley A Arberry, et al.
Biochemical Pharmacology|June 4, 2016
Interactions between amiodarone and the hERG potassium channel pore determined with mutagenesis and in silico dockingYihong Zhang, Charlotte K Colenso, Aziza El Harchi, et al.
FEBS Letters|July 16, 2003
Preferential closed channel blockade of HERG potassium currents by chemically synthesised BeKm-1 scorpion toxinJames T Milnes, Christopher E Dempsey, John M Ridley, et al.
Pacing and Clinical Electrophysiology : PACE|January 16, 2016
Compound Heterozygous Triadin Mutation Causing Cardiac Arrest in Two SiblingsMark A Walsh, Alan G Stuart, Helene B Schlecht, et al.
Molecular Pharmacology|August 17, 2004
The low-potency, voltage-dependent HERG blocker propafenone--molecular determinants and drug trappingHarry J Witchel, Christopher E Dempsey, Richard B Sessions, et al.
Heart Rhythm|June 15, 2017
Atrial-ventricular differences in rabbit cardiac voltage-gated Na<sup>+</sup> currents: Basis for atrial-selective block by ranolazineRachel E Caves, Hongwei Cheng, Stéphanie C Choisy, et al.
Circulation. Arrhythmia and Electrophysiology|August 25, 2011
Atrial remodeling and the substrate for atrial fibrillation in rat hearts with elevated afterloadShang-Jin Kim, Stéphanie C M Choisy, Palash Barman, et al.
British Journal of Pharmacology|February 14, 2006
Mechanism of hERG K+ channel blockade by the fluoroquinolone antibiotic moxifloxacinAri J Alexandrou, Rona S Duncan, Anneli Sullivan, et al.
Molecular and Cellular Neurosciences|April 17, 2007
The sodium channel Nav1.5a is the predominant isoform expressed in adult mouse dorsal root ganglia and exhibits distinct inactivation properties from the full-length Nav1.5 channelNiall C H Kerr, Zhan Gao, Fiona E Holmes, et al.
Pageof 23

Showing results (171-180 of 221) with videos related to

Sort By:
Pageof 23
Interface Focus|December 18, 2023
Evaluating pro-arrhythmogenic effects of the T634S-hERG mutation: insights from a simulation studyWei Hu, Wenfeng Zhang, Kevin Zhang, et al.
Molecular Pharmacology|August 24, 2004
Evidence for a novel K(+) channel modulated by alpha(1A)-adrenoceptors in cardiac myocytesStéphanie C M Choisy, Jules C Hancox, Lesley A Arberry, et al.
Biochemical Pharmacology|June 4, 2016
Interactions between amiodarone and the hERG potassium channel pore determined with mutagenesis and in silico dockingYihong Zhang, Charlotte K Colenso, Aziza El Harchi, et al.
FEBS Letters|July 16, 2003
Preferential closed channel blockade of HERG potassium currents by chemically synthesised BeKm-1 scorpion toxinJames T Milnes, Christopher E Dempsey, John M Ridley, et al.
Pacing and Clinical Electrophysiology : PACE|January 16, 2016
Compound Heterozygous Triadin Mutation Causing Cardiac Arrest in Two SiblingsMark A Walsh, Alan G Stuart, Helene B Schlecht, et al.
Molecular Pharmacology|August 17, 2004
The low-potency, voltage-dependent HERG blocker propafenone--molecular determinants and drug trappingHarry J Witchel, Christopher E Dempsey, Richard B Sessions, et al.
Heart Rhythm|June 15, 2017
Atrial-ventricular differences in rabbit cardiac voltage-gated Na<sup>+</sup> currents: Basis for atrial-selective block by ranolazineRachel E Caves, Hongwei Cheng, Stéphanie C Choisy, et al.
Circulation. Arrhythmia and Electrophysiology|August 25, 2011
Atrial remodeling and the substrate for atrial fibrillation in rat hearts with elevated afterloadShang-Jin Kim, Stéphanie C M Choisy, Palash Barman, et al.
British Journal of Pharmacology|February 14, 2006
Mechanism of hERG K+ channel blockade by the fluoroquinolone antibiotic moxifloxacinAri J Alexandrou, Rona S Duncan, Anneli Sullivan, et al.
Molecular and Cellular Neurosciences|April 17, 2007
The sodium channel Nav1.5a is the predominant isoform expressed in adult mouse dorsal root ganglia and exhibits distinct inactivation properties from the full-length Nav1.5 channelNiall C H Kerr, Zhan Gao, Fiona E Holmes, et al.
Pageof 23