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Eric Schulze

Showing results (31-40 of 155) with videos related to

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International Journal of Legal Medicine|January 7, 2006
Cardiac arrhythmias and sudden death in infancy: implication for the medicolegal investigationHorst Wedekind, Eric Schulze-Bahr, Volker Debus, et al.
Herzschrittmachertherapie & Elektrophysiologie|September 22, 2012
Inherited long QT syndrome: clinical manifestation, genetic diagnostics, and therapySven Zumhagen, Birgit Stallmeyer, Corinna Friedrich, et al.
Pacing and Clinical Electrophysiology : PACE|October 1, 2003
Electrical alternans in long QT syndrome resembling a Brugada syndrome patternEric Schulze-Bahr, Karl-Albert Zoelch, Lars Eckardt, et al.
Nanoscale|May 2, 2023
Bilayer lipid membrane formation on surface assemblies with sparsely distributed tethersMartynas Gavutis, Eric Schulze-Niemand, Hung-Hsun Lee, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|March 5, 2016
Tpeak-Tend interval and Tpeak-Tend/QT ratio in patients with Brugada syndromeSven Zumhagen, Eva Maria Zeidler, Birgit Stallmeyer, et al.
International Journal of Molecular Sciences|October 28, 2023
The W101C <i>KCNJ5</i> Mutation Induces Slower Pacing by Constitutively Active GIRK Channels in hiPSC-Derived CardiomyocytesAnne Kayser, Sven Dittmann, Tomo Šarić, et al.
Stem Cell Research|May 25, 2025
Generation of human induced pluripotent stem cell (hiPSC) lines (UKMi009-A and UKMi011-A) harboring a homozygous and heterozygous HCN4 variant from a family with inherited sinus node dysfunction (SND)Jassin Hamidi, Sven Dittmann, Elisabeth Krämer, et al.
Human Mutation|June 22, 2010
A homozygous SCN5A mutation in a severe, recessive type of cardiac conduction diseaseAxel Neu, Michele Eiselt, Matthias Paul, et al.
The Journal of Clinical Investigation|May 17, 2003
Pacemaker channel dysfunction in a patient with sinus node diseaseEric Schulze-Bahr, Axel Neu, Patrick Friederich, et al.
Biochemical and Biophysical Research Communications|August 23, 2019
A cardiac α-actin (ACTC1) p. Gly247Asp mutation inhibits SRF-signaling in vitro in neonatal rat cardiomyocytesAshraf Yusuf Rangrez, Lucia Kilian, Katharina Stiebeling, et al.
Pageof 16

Showing results (31-40 of 155) with videos related to

Sort By:
Pageof 16
International Journal of Legal Medicine|January 7, 2006
Cardiac arrhythmias and sudden death in infancy: implication for the medicolegal investigationHorst Wedekind, Eric Schulze-Bahr, Volker Debus, et al.
Herzschrittmachertherapie & Elektrophysiologie|September 22, 2012
Inherited long QT syndrome: clinical manifestation, genetic diagnostics, and therapySven Zumhagen, Birgit Stallmeyer, Corinna Friedrich, et al.
Pacing and Clinical Electrophysiology : PACE|October 1, 2003
Electrical alternans in long QT syndrome resembling a Brugada syndrome patternEric Schulze-Bahr, Karl-Albert Zoelch, Lars Eckardt, et al.
Nanoscale|May 2, 2023
Bilayer lipid membrane formation on surface assemblies with sparsely distributed tethersMartynas Gavutis, Eric Schulze-Niemand, Hung-Hsun Lee, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|March 5, 2016
Tpeak-Tend interval and Tpeak-Tend/QT ratio in patients with Brugada syndromeSven Zumhagen, Eva Maria Zeidler, Birgit Stallmeyer, et al.
International Journal of Molecular Sciences|October 28, 2023
The W101C <i>KCNJ5</i> Mutation Induces Slower Pacing by Constitutively Active GIRK Channels in hiPSC-Derived CardiomyocytesAnne Kayser, Sven Dittmann, Tomo Šarić, et al.
Stem Cell Research|May 25, 2025
Generation of human induced pluripotent stem cell (hiPSC) lines (UKMi009-A and UKMi011-A) harboring a homozygous and heterozygous HCN4 variant from a family with inherited sinus node dysfunction (SND)Jassin Hamidi, Sven Dittmann, Elisabeth Krämer, et al.
Human Mutation|June 22, 2010
A homozygous SCN5A mutation in a severe, recessive type of cardiac conduction diseaseAxel Neu, Michele Eiselt, Matthias Paul, et al.
The Journal of Clinical Investigation|May 17, 2003
Pacemaker channel dysfunction in a patient with sinus node diseaseEric Schulze-Bahr, Axel Neu, Patrick Friederich, et al.
Biochemical and Biophysical Research Communications|August 23, 2019
A cardiac α-actin (ACTC1) p. Gly247Asp mutation inhibits SRF-signaling in vitro in neonatal rat cardiomyocytesAshraf Yusuf Rangrez, Lucia Kilian, Katharina Stiebeling, et al.
Pageof 16