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Matteo Vatta

Showing results (101-110 of 124) with videos related to

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American Heart Journal|September 20, 2015
Genetic mutations in African patients with atrial fibrillation: Rationale and design of the Study of Genetics of Atrial Fibrillation in an African Population (SIGNAL)Gerald S Bloomfield, Tecla M Temu, Constantine O Akwanalo, et al.
Circulation. Arrhythmia and Electrophysiology|August 18, 2009
alpha-1-syntrophin mutation and the long-QT syndrome: a disease of sodium channel disruptionGeru Wu, Tomohiko Ai, Jeffrey J Kim, et al.
Circulation. Arrhythmia and Electrophysiology|August 30, 2012
Loss of function of hNav1.5 by a ZASP1 mutation associated with intraventricular conduction disturbances in left ventricular noncompactionYutao Xi, Tomohiko Ai, Enno De Lange, et al.
Circulation. Arrhythmia and Electrophysiology|September 21, 2010
A ZASP missense mutation, S196L, leads to cytoskeletal and electrical abnormalities in a mouse model of cardiomyopathyZhaohui Li, Tomohiko Ai, Kaveh Samani, et al.
Circulation. Genomic and Precision Medicine|March 12, 2020
Variant Interpretation for Dilated Cardiomyopathy: Refinement of the American College of Medical Genetics and Genomics/ClinGen Guidelines for the DCM Precision Medicine StudyAna Morales, Daniel D Kinnamon, Elizabeth Jordan, et al.
Heart Rhythm|January 1, 2010
KCNE2 modulation of Kv4.3 current and its potential role in fatal rhythm disordersJie Wu, Wataru Shimizu, Wei-Guang Ding, et al.
Journal of the American College of Cardiology|October 19, 2010
Nebulette mutations are associated with dilated cardiomyopathy and endocardial fibroelastosisEnkhsaikhan Purevjav, Jaquelin Varela, Micaela Morgado, et al.
Circulation|April 19, 2006
Beta2-adrenergic receptor genetic variants and risk of sudden cardiac deathNona Sotoodehnia, David S Siscovick, Matteo Vatta, et al.
Scientific Reports|June 14, 2018
Phosphorylation of the RSRSP stretch is critical for splicing regulation by RNA-Binding Motif Protein 20 (RBM20) through nuclear localizationRie Murayama, Mariko Kimura-Asami, Marina Togo-Ohno, et al.
Molecular Genetics and Metabolism|October 22, 2003
Mutations in the muscle LIM protein and alpha-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosisBhagyalaxmi Mohapatra, Shinawe Jimenez, Jiuann Huey Lin, et al.
Pageof 13

Showing results (101-110 of 124) with videos related to

Sort By:
Pageof 13
American Heart Journal|September 20, 2015
Genetic mutations in African patients with atrial fibrillation: Rationale and design of the Study of Genetics of Atrial Fibrillation in an African Population (SIGNAL)Gerald S Bloomfield, Tecla M Temu, Constantine O Akwanalo, et al.
Circulation. Arrhythmia and Electrophysiology|August 18, 2009
alpha-1-syntrophin mutation and the long-QT syndrome: a disease of sodium channel disruptionGeru Wu, Tomohiko Ai, Jeffrey J Kim, et al.
Circulation. Arrhythmia and Electrophysiology|August 30, 2012
Loss of function of hNav1.5 by a ZASP1 mutation associated with intraventricular conduction disturbances in left ventricular noncompactionYutao Xi, Tomohiko Ai, Enno De Lange, et al.
Circulation. Arrhythmia and Electrophysiology|September 21, 2010
A ZASP missense mutation, S196L, leads to cytoskeletal and electrical abnormalities in a mouse model of cardiomyopathyZhaohui Li, Tomohiko Ai, Kaveh Samani, et al.
Circulation. Genomic and Precision Medicine|March 12, 2020
Variant Interpretation for Dilated Cardiomyopathy: Refinement of the American College of Medical Genetics and Genomics/ClinGen Guidelines for the DCM Precision Medicine StudyAna Morales, Daniel D Kinnamon, Elizabeth Jordan, et al.
Heart Rhythm|January 1, 2010
KCNE2 modulation of Kv4.3 current and its potential role in fatal rhythm disordersJie Wu, Wataru Shimizu, Wei-Guang Ding, et al.
Journal of the American College of Cardiology|October 19, 2010
Nebulette mutations are associated with dilated cardiomyopathy and endocardial fibroelastosisEnkhsaikhan Purevjav, Jaquelin Varela, Micaela Morgado, et al.
Circulation|April 19, 2006
Beta2-adrenergic receptor genetic variants and risk of sudden cardiac deathNona Sotoodehnia, David S Siscovick, Matteo Vatta, et al.
Scientific Reports|June 14, 2018
Phosphorylation of the RSRSP stretch is critical for splicing regulation by RNA-Binding Motif Protein 20 (RBM20) through nuclear localizationRie Murayama, Mariko Kimura-Asami, Marina Togo-Ohno, et al.
Molecular Genetics and Metabolism|October 22, 2003
Mutations in the muscle LIM protein and alpha-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosisBhagyalaxmi Mohapatra, Shinawe Jimenez, Jiuann Huey Lin, et al.
Pageof 13