Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Alessandra Rampazzo

Showing results (11-20 of 60) with videos related to

Pageof 6
Sort By:
International Journal of Molecular Sciences|May 15, 2020
Modeling Cardiovascular Diseases with hiPSC-Derived Cardiomyocytes in 2D and 3D CulturesClaudia Sacchetto, Libero Vitiello, Leon J de Windt, et al.
Oncotarget|September 27, 2017
Wnt/β-catenin pathway in arrhythmogenic cardiomyopathyAlessandra Lorenzon, Martina Calore, Giulia Poloni, et al.
International Journal of Molecular Sciences|October 23, 2021
Recent Advances in CRISPR/Cas9-Based Genome Editing Tools for Cardiac DiseasesJuliët Schreurs, Claudia Sacchetto, Robin M W Colpaert, et al.
Future Cardiology|May 14, 2010
From molecular mechanisms of cardiac development to genetic substrate of congenital heart diseasesAntonella Cecchetto, Alessandra Rampazzo, Annalisa Angelini, et al.
Annals of Biomedical Engineering|December 21, 2018
Transcriptomic Characterization of a Human In Vitro Model of Arrhythmogenic Cardiomyopathy Under Topological and Mechanical StimuliSebastian Martewicz, Camilla Luni, Elena Serena, 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|April 20, 2007
Homozygous SCN5A mutation in Brugada syndrome with monomorphic ventricular tachycardia and structural heart abnormalitiesGianfranco Frigo, Alessandra Rampazzo, Barbara Bauce, et al.
Clinical Chemistry|May 8, 2004
Denaturing HPLC-based approach for detecting RYR2 mutations involved in malignant arrhythmiasAlessia Bagattin, Caterina Veronese, Barbara Bauce, et al.
Journal of Clinical Medicine|June 2, 2021
Hypertrophic Cardiomyopathy and Primary Restrictive Cardiomyopathy: Similarities, Differences and PhenocopiesRiccardo Vio, Annalisa Angelini, Cristina Basso, et al.
Journal of Applied Genetics|June 30, 2021
Pathogenic variants in plakophilin-2 gene (PKP2) are associated with better survival in arrhythmogenic right ventricular cardiomyopathyElżbieta K Biernacka, Karolina Borowiec, Maria Franaszczyk, et al.
Journal of Medical Genetics|March 6, 2015
A founder MYBPC3 mutation results in HCM with a high risk of sudden death after the fourth decade of lifeChiara Calore, Marzia De Bortoli, Chiara Romualdi, et al.
Pageof 6

Showing results (11-20 of 60) with videos related to

Sort By:
Pageof 6
International Journal of Molecular Sciences|May 15, 2020
Modeling Cardiovascular Diseases with hiPSC-Derived Cardiomyocytes in 2D and 3D CulturesClaudia Sacchetto, Libero Vitiello, Leon J de Windt, et al.
Oncotarget|September 27, 2017
Wnt/β-catenin pathway in arrhythmogenic cardiomyopathyAlessandra Lorenzon, Martina Calore, Giulia Poloni, et al.
International Journal of Molecular Sciences|October 23, 2021
Recent Advances in CRISPR/Cas9-Based Genome Editing Tools for Cardiac DiseasesJuliët Schreurs, Claudia Sacchetto, Robin M W Colpaert, et al.
Future Cardiology|May 14, 2010
From molecular mechanisms of cardiac development to genetic substrate of congenital heart diseasesAntonella Cecchetto, Alessandra Rampazzo, Annalisa Angelini, et al.
Annals of Biomedical Engineering|December 21, 2018
Transcriptomic Characterization of a Human In Vitro Model of Arrhythmogenic Cardiomyopathy Under Topological and Mechanical StimuliSebastian Martewicz, Camilla Luni, Elena Serena, 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|April 20, 2007
Homozygous SCN5A mutation in Brugada syndrome with monomorphic ventricular tachycardia and structural heart abnormalitiesGianfranco Frigo, Alessandra Rampazzo, Barbara Bauce, et al.
Clinical Chemistry|May 8, 2004
Denaturing HPLC-based approach for detecting RYR2 mutations involved in malignant arrhythmiasAlessia Bagattin, Caterina Veronese, Barbara Bauce, et al.
Journal of Clinical Medicine|June 2, 2021
Hypertrophic Cardiomyopathy and Primary Restrictive Cardiomyopathy: Similarities, Differences and PhenocopiesRiccardo Vio, Annalisa Angelini, Cristina Basso, et al.
Journal of Applied Genetics|June 30, 2021
Pathogenic variants in plakophilin-2 gene (PKP2) are associated with better survival in arrhythmogenic right ventricular cardiomyopathyElżbieta K Biernacka, Karolina Borowiec, Maria Franaszczyk, et al.
Journal of Medical Genetics|March 6, 2015
A founder MYBPC3 mutation results in HCM with a high risk of sudden death after the fourth decade of lifeChiara Calore, Marzia De Bortoli, Chiara Romualdi, et al.
Pageof 6