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Stem Cell Research
|
October 27, 2023
Patient-derived stem cell line UKMi005-A (hiPSC) harboring a non-synonymous heterozygous KCNJ5 gene variant
Anne Kayser, Sven Dittmann, Andreas van Impel, et al.
BMC Cardiovascular Disorders
|
April 14, 2021
A rare cause of sudden unexpected death syndrome (SUDS) in the first year of life: endomyocardial fibroelastosis (EFE) due to two compound heterozygous MYBPC3 mutations
Benno Hartung, Anne Tank, Sven Dittmann, et al.
Chembiochem : a European Journal of Chemical Biology
|
October 24, 2019
Chemical-Shift Perturbations Reflect Bile Acid Binding to Norovirus Coat Protein: Recognition Comes in Different Flavors
Robert Creutznacher, Eric Schulze, Georg Wallmann, et al.
Journal of Chemical Information and Modeling
|
January 9, 2025
Activation and Reactivity of the Deubiquitinylase OTU Cezanne-2 from MD Simulations and QM/MM Calculations
Metehan Ilter, Andrés M Escorcia, Eric Schulze-Niemand, et al.
Journal of Cardiovascular Translational Research
|
October 1, 2025
A MATLAB Algorithm to Automatically Estimate the QT Interval and Other ECG Parameters and Validation Using a Machine Learning Approach in Congenital Long-QT Syndrome
Elinor Tzvi-Minker, Sven Dittmann, Corinna Rickert, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology
|
July 11, 2013
A common structural component for β-subunit mediated modulation of slow inactivation in different KV channels
Nathalie Strutz-Seebohm, Ulrike Henrion, Nicole Schmitt, et al.
Pflugers Archiv : European Journal of Physiology
|
November 19, 2014
The role of acid-sensitive two-pore domain potassium channels in cardiac electrophysiology: focus on arrhythmias
Niels Decher, Aytug K Kiper, Caroline Rolfes, et al.
Herz
|
April 17, 2009
Genes causing inherited forms of cardiomyopathies. A current compendium
Matthias Paul, Sven Zumhagen, Birgit Stallmeyer, et al.
Current Sports Medicine Reports
|
July 2, 2003
The long QT syndrome: considerations in the athletic population
Eric Schulze-Bahr, Gerold Mönnig, Lars Eckardt, et al.
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 phenotyping
Elinor Tzvi-Minker, Sven Dittmann, Christian Krijger Juárez, et al.
Page
of 16
Search research articles
Search
Showing results (21-30 of 155) with videos related to
Sort By:
Page
of 16
Stem Cell Research
|
October 27, 2023
Patient-derived stem cell line UKMi005-A (hiPSC) harboring a non-synonymous heterozygous KCNJ5 gene variant
Anne Kayser, Sven Dittmann, Andreas van Impel, et al.
BMC Cardiovascular Disorders
|
April 14, 2021
A rare cause of sudden unexpected death syndrome (SUDS) in the first year of life: endomyocardial fibroelastosis (EFE) due to two compound heterozygous MYBPC3 mutations
Benno Hartung, Anne Tank, Sven Dittmann, et al.
Chembiochem : a European Journal of Chemical Biology
|
October 24, 2019
Chemical-Shift Perturbations Reflect Bile Acid Binding to Norovirus Coat Protein: Recognition Comes in Different Flavors
Robert Creutznacher, Eric Schulze, Georg Wallmann, et al.
Journal of Chemical Information and Modeling
|
January 9, 2025
Activation and Reactivity of the Deubiquitinylase OTU Cezanne-2 from MD Simulations and QM/MM Calculations
Metehan Ilter, Andrés M Escorcia, Eric Schulze-Niemand, et al.
Journal of Cardiovascular Translational Research
|
October 1, 2025
A MATLAB Algorithm to Automatically Estimate the QT Interval and Other ECG Parameters and Validation Using a Machine Learning Approach in Congenital Long-QT Syndrome
Elinor Tzvi-Minker, Sven Dittmann, Corinna Rickert, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology
|
July 11, 2013
A common structural component for β-subunit mediated modulation of slow inactivation in different KV channels
Nathalie Strutz-Seebohm, Ulrike Henrion, Nicole Schmitt, et al.
Pflugers Archiv : European Journal of Physiology
|
November 19, 2014
The role of acid-sensitive two-pore domain potassium channels in cardiac electrophysiology: focus on arrhythmias
Niels Decher, Aytug K Kiper, Caroline Rolfes, et al.
Herz
|
April 17, 2009
Genes causing inherited forms of cardiomyopathies. A current compendium
Matthias Paul, Sven Zumhagen, Birgit Stallmeyer, et al.
Current Sports Medicine Reports
|
July 2, 2003
The long QT syndrome: considerations in the athletic population
Eric Schulze-Bahr, Gerold Mönnig, Lars Eckardt, et al.
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 phenotyping
Elinor Tzvi-Minker, Sven Dittmann, Christian Krijger Juárez, et al.
Page
of 16