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Physiological Reports|April 9, 2026
Models of the human heart for biomedical research: Opportunities and challengesKatrin Streckfuss-Bömeke, Laura C Zelarayán, Renate B Schnabel, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|December 20, 2011
In vitro modeling of ryanodine receptor 2 dysfunction using human induced pluripotent stem cellsAzra Fatima, Guoxing Xu, Kaifeng Shao, et al.
European Journal of Heart Failure|July 14, 2011
Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart FailureStephan Waldmüller, Jeanette Erdmann, Priska Binner, et al.
European Heart Journal|March 7, 2014
The TMEM43 Newfoundland mutation p.S358L causing ARVC-5 was imported from Europe and increases the stiffness of the cell nucleusHendrik Milting, Bärbel Klauke, Alex Hoerby Christensen, et al.
Science Translational Medicine|November 3, 2021
Truncated titin proteins and titin haploinsufficiency are targets for functional recovery in human cardiomyopathy due to TTN mutationsAndrey Fomin, Anna Gärtner, Lukas Cyganek, et al.
Nature Cardiovascular Research|February 24, 2025
The cellular and molecular cardiac tissue responses in human inflammatory cardiomyopathies after SARS-CoV-2 infection and COVID-19 vaccinationHenrike Maatz, Eric L Lindberg, Eleonora Adami, et al.
JACC. Cardiovascular Imaging|January 16, 2022
18F-GP1 Positron Emission Tomography and Bioprosthetic Aortic Valve ThrombusRong Bing, Marcus-André Deutsch, Stephanie L Sellers, et al.
Journal of Cardiovascular Translational Research|June 25, 2026
Tracing the pathogenic PLN p.(Arg14del) variant across the globe; more than just a local curiosityEsmée van Drie, Freyja H M van Lint, Rob Zwart, et al.
Nature|August 10, 2022
Spatial multi-omic map of human myocardial infarctionChristoph Kuppe, Ricardo O Ramirez Flores, Zhijian Li, et al.
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