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Morten Grunnet

Showing results (91-100 of 132) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 2004
Does KCNE5 play a role in long QT syndrome?Jacob Hofman-Bang, Thomas Jespersen, Morten Grunnet, et al.
Journal of Cardiovascular Pharmacology|April 10, 2015
Antiarrhythmic Mechanisms of SK Channel Inhibition in the Rat AtriumLasse Skibsbye, Xiaodong Wang, Lene Nygaard Axelsen, et al.
Frontiers in Pharmacology|March 18, 2020
The K<sub>Ca</sub>2 Channel Inhibitor AP30663 Selectively Increases Atrial Refractoriness, Converts Vernakalant-Resistant Atrial Fibrillation and Prevents Its Reinduction in Conscious PigsJonas Goldin Diness, Jeppe Egedal Kirchhoff, Tobias Speerschneider, et al.
Brain Research|October 26, 2013
Biophysical and pharmacological characterization of α6-containing nicotinic acetylcholine receptors expressed in HEK293 cellsAndreas H Rasmussen, Dorte Strøbæk, Tino Dyhring, et al.
Biochemical and Biophysical Research Communications|February 16, 2006
The corticosteroid hormone induced factor: a new modulator of KCNQ1 channels?Thomas Jespersen, Morten Grunnet, Hanne B Rasmussen, et al.
Frontiers in Pharmacology|June 9, 2020
Inhibition of K<sub>Ca</sub>2 Channels Decreased the Risk of Ventricular Arrhythmia in the Guinea Pig Heart During Induced HypokalemiaJonas Goldin Diness, Lea Abildgaard, Sofia Hammami Bomholtz, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|March 7, 2014
Flecainide provocation reveals concealed brugada syndrome in a long QT syndrome family with a novel L1786Q mutation in SCN5AJørgen K Kanters, Lei Yuan, Paula L Hedley, et al.
Biochemical and Biophysical Research Communications|October 31, 2007
Characterizations of a loss-of-function mutation in the Kir3.4 channel subunitKirstine Calloe, Lasse Steen Ravn, Nicole Schmitt, et al.
Heart Rhythm|October 29, 2005
Functional assessment of compound mutations in the KCNQ1 and KCNH2 genes associated with long QT syndromeMorten Grunnet, Elijah Raphael Behr, Kirstine Calloe, et al.
British Journal of Pharmacology|September 20, 2017
A new negative allosteric modulator, AP14145, for the study of small conductance calcium-activated potassium (K<sub>Ca</sub> 2) channelsRafel Simó-Vicens, Jeppe E Kirchhoff, Bernardo Dolce, et al.
Pageof 14

Showing results (91-100 of 132) with videos related to

Sort By:
Pageof 14
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 2004
Does KCNE5 play a role in long QT syndrome?Jacob Hofman-Bang, Thomas Jespersen, Morten Grunnet, et al.
Journal of Cardiovascular Pharmacology|April 10, 2015
Antiarrhythmic Mechanisms of SK Channel Inhibition in the Rat AtriumLasse Skibsbye, Xiaodong Wang, Lene Nygaard Axelsen, et al.
Frontiers in Pharmacology|March 18, 2020
The K<sub>Ca</sub>2 Channel Inhibitor AP30663 Selectively Increases Atrial Refractoriness, Converts Vernakalant-Resistant Atrial Fibrillation and Prevents Its Reinduction in Conscious PigsJonas Goldin Diness, Jeppe Egedal Kirchhoff, Tobias Speerschneider, et al.
Brain Research|October 26, 2013
Biophysical and pharmacological characterization of α6-containing nicotinic acetylcholine receptors expressed in HEK293 cellsAndreas H Rasmussen, Dorte Strøbæk, Tino Dyhring, et al.
Biochemical and Biophysical Research Communications|February 16, 2006
The corticosteroid hormone induced factor: a new modulator of KCNQ1 channels?Thomas Jespersen, Morten Grunnet, Hanne B Rasmussen, et al.
Frontiers in Pharmacology|June 9, 2020
Inhibition of K<sub>Ca</sub>2 Channels Decreased the Risk of Ventricular Arrhythmia in the Guinea Pig Heart During Induced HypokalemiaJonas Goldin Diness, Lea Abildgaard, Sofia Hammami Bomholtz, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|March 7, 2014
Flecainide provocation reveals concealed brugada syndrome in a long QT syndrome family with a novel L1786Q mutation in SCN5AJørgen K Kanters, Lei Yuan, Paula L Hedley, et al.
Biochemical and Biophysical Research Communications|October 31, 2007
Characterizations of a loss-of-function mutation in the Kir3.4 channel subunitKirstine Calloe, Lasse Steen Ravn, Nicole Schmitt, et al.
Heart Rhythm|October 29, 2005
Functional assessment of compound mutations in the KCNQ1 and KCNH2 genes associated with long QT syndromeMorten Grunnet, Elijah Raphael Behr, Kirstine Calloe, et al.
British Journal of Pharmacology|September 20, 2017
A new negative allosteric modulator, AP14145, for the study of small conductance calcium-activated potassium (K<sub>Ca</sub> 2) channelsRafel Simó-Vicens, Jeppe E Kirchhoff, Bernardo Dolce, et al.
Pageof 14