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Rare Diseases (Austin, Tex.)|October 21, 2015
Human iPS cell models of Jervell and Lange-Nielsen syndromeMilena Bellin, Boris Greber
Biomolecules|October 28, 2023
Advance in Genomics of Rare Genetic DiseasesElena Sommariva, Milena Bellin, Chiara Di Resta
British Journal of Pharmacology|September 20, 2016
Integrating cardiomyocytes from human pluripotent stem cells in safety pharmacology: has the time come?Luca Sala, Milena Bellin, Christine L Mummery
Frontiers in Cardiovascular Medicine|January 6, 2022
Inflammation in the Pathogenesis of Arrhythmogenic Cardiomyopathy: Secondary Event or Active Driver?Viviana Meraviglia, Mireia Alcalde, Oscar Campuzano, et al.
European Journal of Heart Failure|August 8, 2012
Coronary telangiectasia associated with hypertrophic cardiomyopathyAndrea Frustaci, Gerolamo Lanfranchi, Milena Bellin, et al.
Stem Cell Reports|December 18, 2020
Engineered models of the human heart: Directions and challengesJeroen M Stein, Christine L Mummery, Milena Bellin
Biochemical and Biophysical Research Communications|August 7, 2021
Cardiac microtissues from human pluripotent stem cells recapitulate the phenotype of long-QT syndromeElisa Giacomelli, Luca Sala, Dorien Ward-van Oostwaard, et al.
International Journal of Molecular Sciences|November 16, 2018
Large-Scale Simulation of the Phenotypical Variability Induced by Loss-of-Function Long QT Mutations in Human Induced Pluripotent Stem Cell CardiomyocytesMichelangelo Paci, Simona Casini, Milena Bellin, et al.
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