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Isabelle Marty

Showing results (61-70 of 65) with videos related to

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Human Mutation|June 29, 2010
Recessive mutations in RYR1 are a common cause of congenital fiber type disproportionNigel F Clarke, Leigh B Waddell, Sandra T Cooper, et al.
Circulation|June 4, 2014
Single delivery of an adeno-associated viral construct to transfer the CASQ2 gene to knock-in mice affected by catecholaminergic polymorphic ventricular tachycardia is able to cure the disease from birth to advanced ageMarco Denegri, Rossana Bongianino, Francesco Lodola, et al.
Circulation|June 11, 2008
Cardiomyocyte overexpression of neuronal nitric oxide synthase delays transition toward heart failure in response to pressure overload by preserving calcium cyclingXavier Loyer, Ana Maria Gómez, Paul Milliez, et al.
Human Molecular Genetics|March 17, 2012
Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in humanNathalie Roux-Buisson, Marine Cacheux, Anne Fourest-Lieuvin, et al.
Journal of Medical Genetics|September 30, 2020
Clinical phenotype and loss of the slow skeletal muscle troponin T in three new patients with recessive TNNT1 nemaline myopathyJustine Géraud, Klaus Dieterich, John Rendu, et al.
Pageof 7

Showing results (61-70 of 65) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 65 results.
Human Mutation|June 29, 2010
Recessive mutations in RYR1 are a common cause of congenital fiber type disproportionNigel F Clarke, Leigh B Waddell, Sandra T Cooper, et al.
Circulation|June 4, 2014
Single delivery of an adeno-associated viral construct to transfer the CASQ2 gene to knock-in mice affected by catecholaminergic polymorphic ventricular tachycardia is able to cure the disease from birth to advanced ageMarco Denegri, Rossana Bongianino, Francesco Lodola, et al.
Circulation|June 11, 2008
Cardiomyocyte overexpression of neuronal nitric oxide synthase delays transition toward heart failure in response to pressure overload by preserving calcium cyclingXavier Loyer, Ana Maria Gómez, Paul Milliez, et al.
Human Molecular Genetics|March 17, 2012
Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in humanNathalie Roux-Buisson, Marine Cacheux, Anne Fourest-Lieuvin, et al.
Journal of Medical Genetics|September 30, 2020
Clinical phenotype and loss of the slow skeletal muscle troponin T in three new patients with recessive TNNT1 nemaline myopathyJustine Géraud, Klaus Dieterich, John Rendu, et al.
Pageof 7