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

Pierre Lindenbaum

Showing results (21-30 of 43) with videos related to

Pageof 5
Sort By:
Circulation. Cardiovascular Genetics|December 9, 2015
Search for Rare Copy-Number Variants in Congenital Heart Defects Identifies Novel Candidate Genes and a Potential Role for FOXC1 in Patients With Coarctation of the AortaMarta Sanchez-Castro, Hadja Eldjouzi, Eric Charpentier, et al.
Molecular Therapy. Methods & Clinical Development|June 2, 2015
Short-lived recombinant adeno-associated virus transgene expression in dystrophic muscle is associated with oxidative damage to transgene mRNAJean-Baptiste Dupont, Benoit Tournaire, Christophe Georger, et al.
American Journal of Human Genetics|January 6, 2018
Rare Coding Variants in ANGPTL6 Are Associated with Familial Forms of Intracranial AneurysmRomain Bourcier, Solena Le Scouarnec, Stéphanie Bonnaud, et al.
Human Mutation|July 12, 2022
Burden of rare variants in arrhythmogenic cardiomyopathy with right dominant form-associated genes provides new insights for molecular diagnosis and clinical managementAdeline Goudal, Matilde Karakachoff, Pierre Lindenbaum, et al.
International Journal of Cardiology|January 29, 2016
Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type IXavier Daumy, Mohamed-Yassine Amarouch, Pierre Lindenbaum, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|November 19, 2020
Phenotypic Differences Between Polygenic and Monogenic HypobetalipoproteinemiaAntoine Rimbert, Xavier Vanhoye, Dramane Coulibaly, et al.
Journal of the American Heart Association|June 12, 2016
Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada SyndromeVincent Portero, Solena Le Scouarnec, Zeineb Es-Salah-Lamoureux, et al.
Circulation|July 28, 2022
Identification of a Gain-of-Function <i>LIPC</i> Variant as a Novel Cause of Familial Combined HypocholesterolemiaWieneke Dijk, Mathilde Di Filippo, Sander Kooijman, et al.
Cardiovascular Research|August 4, 2025
Phenotypic spectrum of cardiac conduction disturbance and cardiomyopathy linked to titin canonical splice-site variantsTaisuke Ishikawa, Hiroki Kimoto, Akiko Seki, et al.
Human Molecular Genetics|February 5, 2015
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndromeSolena Le Scouarnec, Matilde Karakachoff, Jean-Baptiste Gourraud, et al.
Pageof 5

Showing results (21-30 of 43) with videos related to

Sort By:
Pageof 5
Circulation. Cardiovascular Genetics|December 9, 2015
Search for Rare Copy-Number Variants in Congenital Heart Defects Identifies Novel Candidate Genes and a Potential Role for FOXC1 in Patients With Coarctation of the AortaMarta Sanchez-Castro, Hadja Eldjouzi, Eric Charpentier, et al.
Molecular Therapy. Methods & Clinical Development|June 2, 2015
Short-lived recombinant adeno-associated virus transgene expression in dystrophic muscle is associated with oxidative damage to transgene mRNAJean-Baptiste Dupont, Benoit Tournaire, Christophe Georger, et al.
American Journal of Human Genetics|January 6, 2018
Rare Coding Variants in ANGPTL6 Are Associated with Familial Forms of Intracranial AneurysmRomain Bourcier, Solena Le Scouarnec, Stéphanie Bonnaud, et al.
Human Mutation|July 12, 2022
Burden of rare variants in arrhythmogenic cardiomyopathy with right dominant form-associated genes provides new insights for molecular diagnosis and clinical managementAdeline Goudal, Matilde Karakachoff, Pierre Lindenbaum, et al.
International Journal of Cardiology|January 29, 2016
Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type IXavier Daumy, Mohamed-Yassine Amarouch, Pierre Lindenbaum, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|November 19, 2020
Phenotypic Differences Between Polygenic and Monogenic HypobetalipoproteinemiaAntoine Rimbert, Xavier Vanhoye, Dramane Coulibaly, et al.
Journal of the American Heart Association|June 12, 2016
Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada SyndromeVincent Portero, Solena Le Scouarnec, Zeineb Es-Salah-Lamoureux, et al.
Circulation|July 28, 2022
Identification of a Gain-of-Function <i>LIPC</i> Variant as a Novel Cause of Familial Combined HypocholesterolemiaWieneke Dijk, Mathilde Di Filippo, Sander Kooijman, et al.
Cardiovascular Research|August 4, 2025
Phenotypic spectrum of cardiac conduction disturbance and cardiomyopathy linked to titin canonical splice-site variantsTaisuke Ishikawa, Hiroki Kimoto, Akiko Seki, et al.
Human Molecular Genetics|February 5, 2015
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndromeSolena Le Scouarnec, Matilde Karakachoff, Jean-Baptiste Gourraud, et al.
Pageof 5