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European Journal of Human Genetics : EJHG|August 13, 2015
Plakophilin-2 c.419C>T and risk of heart failure and arrhythmias in the general populationAlex Hørby Christensen, Pia Rørbœk Kamstrup, Estelle Gandjbakhch, 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|July 17, 2013
Screening of genes encoding junctional candidates in arrhythmogenic right ventricular cardiomyopathy/dysplasiaEstelle Gandjbakhch, Alexia Vite, Françoise Gary, 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|December 18, 2019
Desmoglein-2 mutations in propeptide cleavage-site causes arrhythmogenic right ventricular cardiomyopathy/dysplasia by impairing extracellular 1-dependent desmosomal interactions upon cellular stressAlexia Vite, Estelle Gandjbakhch, Tiphaine Hery, et al.
The Journal of Infectious Diseases|November 4, 2006
Association between ABCC2 gene haplotypes and tenofovir-induced proximal tubulopathyHassane Izzedine, Jean-Sebastien Hulot, Eric Villard, 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|January 20, 2009
Sporadic arrhythmogenic right ventricular cardiomyopathy/dysplasia due to a de novo mutationEstelle Gandjbakhch, Véronique Fressart, Géraldine Bertaux, et al.
Stem Cell Research|January 30, 2022
Generation of a heterozygous SCN5A knockout human induced pluripotent stem cell line by CRISPR/Cas9 editionMarie Gizon, Laëtitia Duboscq-Bidot, Lina El Kassar, et al.
Plos One|August 3, 2017
Contribution of exome sequencing for genetic diagnostic in arrhythmogenic right ventricular cardiomyopathy/dysplasiaJoel Fedida, Veronique Fressart, Philippe Charron, et al.
European Heart Journal|June 16, 2009
Mutations in the ANKRD1 gene encoding CARP are responsible for human dilated cardiomyopathyLaëtitia Duboscq-Bidot, Philippe Charron, Volker Ruppert, et al.
International Journal of Molecular Sciences|June 8, 2017
Differential Sarcomere and Electrophysiological Maturation of Human iPSC-Derived Cardiac Myocytes in Monolayer vs. Aggregation-Based Differentiation ProtocolsDorota Jeziorowska, Vincent Fontaine, Charlène Jouve, et al.
Stem Cell Research|February 20, 2021
Generation of iPSC line from MYH7 R403L mutation carrier with severe hypertrophic cardiomyopathy and isogenic CRISPR/Cas9 corrected controlVincent Fontaine, Laetitia Duboscq-Bidot, Charlène Jouve, et al.
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