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Lia Crotti

Showing results (91-100 of 246) with videos related to

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International Journal of Molecular Sciences|July 27, 2022
Mitochondrial a Kinase Anchor Proteins in Cardiovascular Health and Disease: A Review Article on Behalf of the Working Group on Cellular and Molecular Biology of the Heart of the Italian Society of CardiologyRoberta Paolillo, Stefania D'Apice, Gabriele Giacomo Schiattarella, et al.
Stem Cell Research|August 10, 2019
Generation of two human induced pluripotent stem cell (hiPSC) lines from a long QT syndrome South African founder populationManuela Mura, Federica Pisano, Manuela Stefanello, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|November 28, 2017
Contemporary genetic testing in inherited cardiac disease: tools, ethical issues, and clinical applicationsFrancesca Girolami, Giulia Frisso, Matteo Benelli, et al.
Heart Rhythm|February 26, 2011
Transient outward current (I(to)) gain-of-function mutations in the KCND3-encoded Kv4.3 potassium channel and Brugada syndromeJohn R Giudicessi, Dan Ye, David J Tester, et al.
Circulation. Arrhythmia and Electrophysiology|October 8, 2009
Malignant perinatal variant of long-QT syndrome caused by a profoundly dysfunctional cardiac sodium channelDao W Wang, Lia Crotti, Wataru Shimizu, et al.
Circulation|January 11, 2007
Cardiac sodium channel dysfunction in sudden infant death syndromeDao W Wang, Reshma R Desai, Lia Crotti, et al.
Stem Cell Research|April 23, 2019
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi005-A from a patient carrying the KCNQ1-R190W mutationManuela Mura, Yee-Ki Lee, Federica Pisano, et al.
Stem Cell Research|April 12, 2019
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi004-A from a carrier of the KCNQ1-R594Q mutationManuela Mura, Yee-Ki Lee, Federica Pisano, et al.
Journal of the American Heart Association|August 17, 2023
Cardiac Genetic Investigation of Sudden Infant and Early Childhood Death: A Study From Victims to FamiliesMaria-Christina Kotta, Margherita Torchio, Pauline Bayliss, et al.
European Heart Journal|October 12, 2017
Identification of a targeted and testable antiarrhythmic therapy for long-QT syndrome type 2 using a patient-specific cellular modelAshish Mehta, Chrishan J A Ramachandra, Pritpal Singh, et al.
Pageof 25

Showing results (91-100 of 246) with videos related to

Sort By:
Pageof 25
International Journal of Molecular Sciences|July 27, 2022
Mitochondrial a Kinase Anchor Proteins in Cardiovascular Health and Disease: A Review Article on Behalf of the Working Group on Cellular and Molecular Biology of the Heart of the Italian Society of CardiologyRoberta Paolillo, Stefania D'Apice, Gabriele Giacomo Schiattarella, et al.
Stem Cell Research|August 10, 2019
Generation of two human induced pluripotent stem cell (hiPSC) lines from a long QT syndrome South African founder populationManuela Mura, Federica Pisano, Manuela Stefanello, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|November 28, 2017
Contemporary genetic testing in inherited cardiac disease: tools, ethical issues, and clinical applicationsFrancesca Girolami, Giulia Frisso, Matteo Benelli, et al.
Heart Rhythm|February 26, 2011
Transient outward current (I(to)) gain-of-function mutations in the KCND3-encoded Kv4.3 potassium channel and Brugada syndromeJohn R Giudicessi, Dan Ye, David J Tester, et al.
Circulation. Arrhythmia and Electrophysiology|October 8, 2009
Malignant perinatal variant of long-QT syndrome caused by a profoundly dysfunctional cardiac sodium channelDao W Wang, Lia Crotti, Wataru Shimizu, et al.
Circulation|January 11, 2007
Cardiac sodium channel dysfunction in sudden infant death syndromeDao W Wang, Reshma R Desai, Lia Crotti, et al.
Stem Cell Research|April 23, 2019
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi005-A from a patient carrying the KCNQ1-R190W mutationManuela Mura, Yee-Ki Lee, Federica Pisano, et al.
Stem Cell Research|April 12, 2019
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi004-A from a carrier of the KCNQ1-R594Q mutationManuela Mura, Yee-Ki Lee, Federica Pisano, et al.
Journal of the American Heart Association|August 17, 2023
Cardiac Genetic Investigation of Sudden Infant and Early Childhood Death: A Study From Victims to FamiliesMaria-Christina Kotta, Margherita Torchio, Pauline Bayliss, et al.
European Heart Journal|October 12, 2017
Identification of a targeted and testable antiarrhythmic therapy for long-QT syndrome type 2 using a patient-specific cellular modelAshish Mehta, Chrishan J A Ramachandra, Pritpal Singh, et al.
Pageof 25