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Future Cardiology
|
October 7, 2009
Short QT syndrome
Mark J McPate, Harry J Witchel, Jules C Hancox
Journal of Molecular and Cellular Cardiology
|
July 18, 2006
Disopyramide is an effective inhibitor of mutant HERG K+ channels involved in variant 1 short QT syndrome
Mark J McPate, Rona S Duncan, Harry J Witchel, et al.
Pharmacology & Therapeutics
|
July 12, 2008
The hERG potassium channel and hERG screening for drug-induced torsades de pointes
Jules C Hancox, Mark J McPate, Aziza El Harchi, et al.
Plos Computational Biology
|
December 24, 2011
Increased vulnerability of human ventricle to re-entrant excitation in hERG-linked variant 1 short QT syndrome
Ismail Adeniran, Mark J McPate, Harry J Witchel, et al.
Journal of Molecular and Cellular Cardiology
|
March 17, 2009
Action potential clamp and chloroquine sensitivity of mutant Kir2.1 channels responsible for variant 3 short QT syndrome
Aziza El Harchi, Mark J McPate, Yi hong Zhang, et al.
Biochemical and Biophysical Research Communications
|
July 14, 2005
The N588K-HERG K+ channel mutation in the 'short QT syndrome': mechanism of gain-in-function determined at 37 degrees C
Mark J McPate, Rona S Duncan, James T Milnes, et al.
FEBS Letters
|
March 18, 2006
Inhibition of the HERG K+ channel by the antifungal drug ketoconazole depends on channel gating and involves the S6 residue F656
John M Ridley, James T Milnes, Rona S Duncan, et al.
Journal of Cardiovascular Electrophysiology
|
May 12, 2010
Acidosis impairs the protective role of hERG K(+) channels against premature stimulation
Chun Yun Du, Ismail Adeniran, Hongwei Cheng, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Future Cardiology
|
October 7, 2009
Short QT syndrome
Mark J McPate, Harry J Witchel, Jules C Hancox
Journal of Molecular and Cellular Cardiology
|
July 18, 2006
Disopyramide is an effective inhibitor of mutant HERG K+ channels involved in variant 1 short QT syndrome
Mark J McPate, Rona S Duncan, Harry J Witchel, et al.
Pharmacology & Therapeutics
|
July 12, 2008
The hERG potassium channel and hERG screening for drug-induced torsades de pointes
Jules C Hancox, Mark J McPate, Aziza El Harchi, et al.
Plos Computational Biology
|
December 24, 2011
Increased vulnerability of human ventricle to re-entrant excitation in hERG-linked variant 1 short QT syndrome
Ismail Adeniran, Mark J McPate, Harry J Witchel, et al.
Journal of Molecular and Cellular Cardiology
|
March 17, 2009
Action potential clamp and chloroquine sensitivity of mutant Kir2.1 channels responsible for variant 3 short QT syndrome
Aziza El Harchi, Mark J McPate, Yi hong Zhang, et al.
Biochemical and Biophysical Research Communications
|
July 14, 2005
The N588K-HERG K+ channel mutation in the 'short QT syndrome': mechanism of gain-in-function determined at 37 degrees C
Mark J McPate, Rona S Duncan, James T Milnes, et al.
FEBS Letters
|
March 18, 2006
Inhibition of the HERG K+ channel by the antifungal drug ketoconazole depends on channel gating and involves the S6 residue F656
John M Ridley, James T Milnes, Rona S Duncan, et al.
Journal of Cardiovascular Electrophysiology
|
May 12, 2010
Acidosis impairs the protective role of hERG K(+) channels against premature stimulation
Chun Yun Du, Ismail Adeniran, Hongwei Cheng, et al.
Page
of 1