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Eric Schulze

Showing results (51-60 of 155) with videos related to

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Basic Research in Cardiology|January 25, 2016
Human iPS cell model of type 3 long QT syndrome recapitulates drug-based phenotype correctionDaniela Malan, Miao Zhang, Birgit Stallmeyer, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|May 23, 2012
Overlapping cardiac phenotype associated with a familial mutation in the voltage sensor of the KCNQ1 channelUlrike Henrion, Sven Zumhagen, Katja Steinke, et al.
Data in Brief|January 11, 2020
Data on the role of cardiac α-actin (ACTC1) gene mutations on SRF-signalingAshraf Yusuf Rangrez, Lucia Kilian, Katharina Stiebeling, et al.
Cardiovascular Research|June 14, 2002
Body surface potential mapping in patients with Brugada syndrome: right precordial ST segment variations and reverse changes in left precordial leadsHans-Jürgen Bruns, Lars Eckardt, Christian Vahlhaus, et al.
The American Journal of Cardiology|March 8, 2013
Connexin expression patterns in arrhythmogenic right ventricular cardiomyopathyMatthias Paul, Thomas Wichter, Joachim Gerss, et al.
Stem Cell Research|May 22, 2024
Generation of a patient-specific hiPS cell line with heterozygous GNB2 mutation (UKMi003-A) causative for human sinus node dysfunction and a corresponding CRISPR/Cas9-corrected isogenic control (UKMi004-A)Anne Kayser, Sven Dittmann, Jassin Hamidi, et al.
Circulation|November 8, 2006
Genotype-specific onset of arrhythmias in congenital long-QT syndrome: possible therapy implicationsHanno L Tan, Abdennasser Bardai, Wataru Shimizu, et al.
European Heart Journal|May 8, 2007
Role of programmed ventricular stimulation in patients with Brugada syndrome: a meta-analysis of worldwide published dataMatthias Paul, Joachim Gerss, Eric Schulze-Bahr, et al.
Herz|February 8, 2003
Molecular mechanisms of inherited ventricular arrhythmiasThomas Wichter, Eric Schulze-Bahr, Lars Eckardt, et al.
Journal of Cardiology Cases|December 15, 2018
High-dose flecainide with low-dose β-blocker therapy in catecholaminergic polymorphic ventricular tachycardia: A case report and review of the literatureJohannes Steinfurt, Markus-Johann Dechant, Doris Böckelmann, et al.
Pageof 16

Showing results (51-60 of 155) with videos related to

Sort By:
Pageof 16
Basic Research in Cardiology|January 25, 2016
Human iPS cell model of type 3 long QT syndrome recapitulates drug-based phenotype correctionDaniela Malan, Miao Zhang, Birgit Stallmeyer, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|May 23, 2012
Overlapping cardiac phenotype associated with a familial mutation in the voltage sensor of the KCNQ1 channelUlrike Henrion, Sven Zumhagen, Katja Steinke, et al.
Data in Brief|January 11, 2020
Data on the role of cardiac α-actin (ACTC1) gene mutations on SRF-signalingAshraf Yusuf Rangrez, Lucia Kilian, Katharina Stiebeling, et al.
Cardiovascular Research|June 14, 2002
Body surface potential mapping in patients with Brugada syndrome: right precordial ST segment variations and reverse changes in left precordial leadsHans-Jürgen Bruns, Lars Eckardt, Christian Vahlhaus, et al.
The American Journal of Cardiology|March 8, 2013
Connexin expression patterns in arrhythmogenic right ventricular cardiomyopathyMatthias Paul, Thomas Wichter, Joachim Gerss, et al.
Stem Cell Research|May 22, 2024
Generation of a patient-specific hiPS cell line with heterozygous GNB2 mutation (UKMi003-A) causative for human sinus node dysfunction and a corresponding CRISPR/Cas9-corrected isogenic control (UKMi004-A)Anne Kayser, Sven Dittmann, Jassin Hamidi, et al.
Circulation|November 8, 2006
Genotype-specific onset of arrhythmias in congenital long-QT syndrome: possible therapy implicationsHanno L Tan, Abdennasser Bardai, Wataru Shimizu, et al.
European Heart Journal|May 8, 2007
Role of programmed ventricular stimulation in patients with Brugada syndrome: a meta-analysis of worldwide published dataMatthias Paul, Joachim Gerss, Eric Schulze-Bahr, et al.
Herz|February 8, 2003
Molecular mechanisms of inherited ventricular arrhythmiasThomas Wichter, Eric Schulze-Bahr, Lars Eckardt, et al.
Journal of Cardiology Cases|December 15, 2018
High-dose flecainide with low-dose β-blocker therapy in catecholaminergic polymorphic ventricular tachycardia: A case report and review of the literatureJohannes Steinfurt, Markus-Johann Dechant, Doris Böckelmann, et al.
Pageof 16