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Richard Redon

Showing results (61-70 of 131) with videos related to

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Circulation|June 5, 2014
PDZ domain-binding motif regulates cardiomyocyte compartment-specific NaV1.5 channel expression and functionDiana Shy, Ludovic Gillet, Jakob Ogrodnik, et al.
Heart Rhythm|July 2, 2017
Sodium-channel blocker challenge in the familial screening of Brugada syndrome: Safety and predictors of positivityDylan Therasse, Frederic Sacher, Bertrand Petit, et al.
International Journal of Molecular Sciences|May 27, 2023
WGS Revealed Novel <i>BBS5</i> Pathogenic Variants, Missed by WES, Causing Ciliary Structure and Function DefectsAdella Karam, Clarisse Delvallée, Alejandro Estrada-Cuzcano, 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.
Nature Genetics|November 23, 2006
Genome assembly comparison identifies structural variants in the human genomeRazi Khaja, Junjun Zhang, Jeffrey R MacDonald, et al.
European Journal of Human Genetics : EJHG|September 4, 2014
Fine-scale human genetic structure in Western FranceMatilde Karakachoff, Nicolas Duforet-Frebourg, Floriane Simonet, 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.
Basic Research in Cardiology|October 25, 2014
Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutationsDelphine M Béziau, Julien Barc, Thomas O'Hara, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|November 19, 2020
Phenotypic Differences Between Polygenic and Monogenic HypobetalipoproteinemiaAntoine Rimbert, Xavier Vanhoye, Dramane Coulibaly, et al.
Pageof 14

Showing results (61-70 of 131) with videos related to

Sort By:
Pageof 14
Circulation|June 5, 2014
PDZ domain-binding motif regulates cardiomyocyte compartment-specific NaV1.5 channel expression and functionDiana Shy, Ludovic Gillet, Jakob Ogrodnik, et al.
Heart Rhythm|July 2, 2017
Sodium-channel blocker challenge in the familial screening of Brugada syndrome: Safety and predictors of positivityDylan Therasse, Frederic Sacher, Bertrand Petit, et al.
International Journal of Molecular Sciences|May 27, 2023
WGS Revealed Novel <i>BBS5</i> Pathogenic Variants, Missed by WES, Causing Ciliary Structure and Function DefectsAdella Karam, Clarisse Delvallée, Alejandro Estrada-Cuzcano, 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.
Nature Genetics|November 23, 2006
Genome assembly comparison identifies structural variants in the human genomeRazi Khaja, Junjun Zhang, Jeffrey R MacDonald, et al.
European Journal of Human Genetics : EJHG|September 4, 2014
Fine-scale human genetic structure in Western FranceMatilde Karakachoff, Nicolas Duforet-Frebourg, Floriane Simonet, 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.
Basic Research in Cardiology|October 25, 2014
Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutationsDelphine M Béziau, Julien Barc, Thomas O'Hara, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|November 19, 2020
Phenotypic Differences Between Polygenic and Monogenic HypobetalipoproteinemiaAntoine Rimbert, Xavier Vanhoye, Dramane Coulibaly, et al.
Pageof 14