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Lorenzo Monserrat

Showing results (121-130 of 160) with videos related to

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Human Molecular Genetics|May 6, 2025
Rare DCM associated variants in pre-miR-208a disrupt miRNA maturation and functionYolan J Reckman, Jan Haas, Ingeborg van der Made, et al.
Journal of the American Heart Association|May 16, 2020
Familial Recurrent Myocarditis Triggered by Exercise in Patients With a Truncating Variant of the Desmoplakin GeneWolfgang Poller, Jan Haas, Karin Klingel, et al.
The Journal of Biological Chemistry|May 31, 2011
Molecular mechanism of the E99K mutation in cardiac actin (ACTC Gene) that causes apical hypertrophy in man and mouseWeihua Song, Emma Dyer, Daniel J Stuckey, et al.
Heart (British Cardiac Society)|May 4, 2015
Phenotype and prognostic correlations of the converter region mutations affecting the β myosin heavy chainDiego García-Giustiniani, Michael Arad, Martín Ortíz-Genga, et al.
BMC Medicine|November 28, 2025
The European BestAgeing Study on microRNA candidates reveals distinct signatures with diagnostic and prognostic potential in cardiovascular diseaseChristoph Reich, Elham Kayvanpour, Farbod Sedaghat-Hamedani, et al.
International Journal of Cardiology|June 28, 2016
Prognostic role of stress echocardiography in hypertrophic cardiomyopathy: The International Stress Echo RegistryQuirino Ciampi, Iacopo Olivotto, Chiara Gardini, et al.
Circulation. Genomic and Precision Medicine|November 5, 2020
Clinical Profile of Cardiac Involvement in Danon Disease: A Multicenter European RegistryDor Lotan, Joel Salazar-Mendiguchía, Jens Mogensen, et al.
Ebiomedicine|April 8, 2020
Identification, clinical manifestation and structural mechanisms of mutations in AMPK associated cardiac glycogen storage diseaseDan Hu, Dong Hu, Liwen Liu, et al.
Circulation Research|June 15, 2023
iPSC-Based Modeling of Variable Clinical Presentation in Hypertrophic CardiomyopathyRubén Escribá, José M Larrañaga-Moreira, Yvonne Richaud-Patin, et al.
The Pharmacogenomics Journal|April 1, 2022
Combining familial hypercholesterolemia and statin genetic studies as a strategy for the implementation of pharmacogenomics. A multidisciplinary approachLuis Ramudo-Cela, Sara Santana-Martínez, Maite García-Ramos, et al.
Pageof 16

Showing results (121-130 of 160) with videos related to

Sort By:
Pageof 16
Human Molecular Genetics|May 6, 2025
Rare DCM associated variants in pre-miR-208a disrupt miRNA maturation and functionYolan J Reckman, Jan Haas, Ingeborg van der Made, et al.
Journal of the American Heart Association|May 16, 2020
Familial Recurrent Myocarditis Triggered by Exercise in Patients With a Truncating Variant of the Desmoplakin GeneWolfgang Poller, Jan Haas, Karin Klingel, et al.
The Journal of Biological Chemistry|May 31, 2011
Molecular mechanism of the E99K mutation in cardiac actin (ACTC Gene) that causes apical hypertrophy in man and mouseWeihua Song, Emma Dyer, Daniel J Stuckey, et al.
Heart (British Cardiac Society)|May 4, 2015
Phenotype and prognostic correlations of the converter region mutations affecting the β myosin heavy chainDiego García-Giustiniani, Michael Arad, Martín Ortíz-Genga, et al.
BMC Medicine|November 28, 2025
The European BestAgeing Study on microRNA candidates reveals distinct signatures with diagnostic and prognostic potential in cardiovascular diseaseChristoph Reich, Elham Kayvanpour, Farbod Sedaghat-Hamedani, et al.
International Journal of Cardiology|June 28, 2016
Prognostic role of stress echocardiography in hypertrophic cardiomyopathy: The International Stress Echo RegistryQuirino Ciampi, Iacopo Olivotto, Chiara Gardini, et al.
Circulation. Genomic and Precision Medicine|November 5, 2020
Clinical Profile of Cardiac Involvement in Danon Disease: A Multicenter European RegistryDor Lotan, Joel Salazar-Mendiguchía, Jens Mogensen, et al.
Ebiomedicine|April 8, 2020
Identification, clinical manifestation and structural mechanisms of mutations in AMPK associated cardiac glycogen storage diseaseDan Hu, Dong Hu, Liwen Liu, et al.
Circulation Research|June 15, 2023
iPSC-Based Modeling of Variable Clinical Presentation in Hypertrophic CardiomyopathyRubén Escribá, José M Larrañaga-Moreira, Yvonne Richaud-Patin, et al.
The Pharmacogenomics Journal|April 1, 2022
Combining familial hypercholesterolemia and statin genetic studies as a strategy for the implementation of pharmacogenomics. A multidisciplinary approachLuis Ramudo-Cela, Sara Santana-Martínez, Maite García-Ramos, et al.
Pageof 16