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Sven Dittmann

Showing results (11-20 of 39) with videos related to

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Frontiers in Cardiovascular Medicine|May 11, 2026
Polygenic risk modulates myocardial repolarization and T-wave geometry in congenital long-QT syndrome type 1: evidence from digital ECG phenotypingElinor Tzvi-Minker, Sven Dittmann, Christian Krijger Juárez, 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.
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.
Inflammation Research : Official Journal of the European Histamine Research Society ... [Et Al.]|December 10, 2013
Effect of lovastatin on coxsackievirus B3 infection in human endothelial cellsBianca Werner, Sven Dittmann, Carsten Funke, et al.
The Journal of General Virology|April 16, 2010
Antiviral effect of Bosentan and Valsartan during coxsackievirus B3 infection of human endothelial cellsCarsten Funke, Martin Farr, Bianca Werner, et al.
Frontiers in Cardiovascular Medicine|February 18, 2025
Unusual hypertrophic cardiomyopathy: case report of an early onset wild-type ATTR amyloidosis accompanied by a chromosomal duplication involving the <i>MYH6</i> and <i>MYH7</i> geneJassin Hamidi, Yvonne Hanel, Sven Dittmann, 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.
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.
JACC. Cardiovascular Imaging|September 16, 2023
Possible Causes and Clinical Relevance of a "Ring-Like" Late Gadolinium Enhancement PatternMichael Bietenbeck, Claudia Meier, Dennis Korthals, et al.
Pageof 4

Showing results (11-20 of 39) with videos related to

Sort By:
Pageof 4
Frontiers in Cardiovascular Medicine|May 11, 2026
Polygenic risk modulates myocardial repolarization and T-wave geometry in congenital long-QT syndrome type 1: evidence from digital ECG phenotypingElinor Tzvi-Minker, Sven Dittmann, Christian Krijger Juárez, 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.
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.
Inflammation Research : Official Journal of the European Histamine Research Society ... [Et Al.]|December 10, 2013
Effect of lovastatin on coxsackievirus B3 infection in human endothelial cellsBianca Werner, Sven Dittmann, Carsten Funke, et al.
The Journal of General Virology|April 16, 2010
Antiviral effect of Bosentan and Valsartan during coxsackievirus B3 infection of human endothelial cellsCarsten Funke, Martin Farr, Bianca Werner, et al.
Frontiers in Cardiovascular Medicine|February 18, 2025
Unusual hypertrophic cardiomyopathy: case report of an early onset wild-type ATTR amyloidosis accompanied by a chromosomal duplication involving the <i>MYH6</i> and <i>MYH7</i> geneJassin Hamidi, Yvonne Hanel, Sven Dittmann, 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.
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.
JACC. Cardiovascular Imaging|September 16, 2023
Possible Causes and Clinical Relevance of a "Ring-Like" Late Gadolinium Enhancement PatternMichael Bietenbeck, Claudia Meier, Dennis Korthals, et al.
Pageof 4