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

Simon Lecointe

Showing results (1-10 of 15) with videos related to

Pageof 2
Sort By:
Structure (London, England : 1993)|October 23, 2018
Non-syndromic Mitral Valve Dysplasia Mutation Changes the Force Resilience and Interaction of Human Filamin ATatu J K Haataja, Rafael C Bernardi, Simon Lecointe, et al.
Biophysical Journal|September 23, 2019
Critical Structural Defects Explain Filamin A Mutations Causing Mitral Valve DysplasiaTatu J K Haataja, Romain Capoulade, Simon Lecointe, et al.
Journal of Cardiovascular Translational Research|July 21, 2011
Filamin-a-related myxomatous mitral valve dystrophy: genetic, echocardiographic and functional aspectsAurélie Lardeux, Florence Kyndt, Simon Lecointe, et al.
Biochimica Et Biophysica Acta. Molecular Cell Research|March 22, 2017
The alternatively spliced LRRFIP1 Isoform-1 is a key regulator of the Wnt/β-catenin transcription pathwayPauline Labbé, Emilie Faure, Simon Lecointe, et al.
Atherosclerosis|May 16, 2016
Identification of novel APOB mutations by targeted next-generation sequencing for the molecular diagnosis of familial hypobetalipoproteinemiaAntoine Rimbert, Matthieu Pichelin, Simon Lecointe, 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.
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.
Cardiovascular Research|August 24, 2022
Multimodality imaging and transcriptomics to phenotype mitral valve dystrophy in a unique knock-in Filamin-A rat modelConstance Delwarde, Claire Toquet, Pascal Aumond, et al.
Circulation. Genomic and Precision Medicine|March 7, 2020
Genetic Association Analyses Highlight <i>IL6</i>, <i>ALPL</i>, and <i>NAV1</i> As 3 New Susceptibility Genes Underlying Calcific Aortic Valve StenosisSébastien Thériault, Christian Dina, David Messika-Zeitoun, et al.
European Heart Journal|October 12, 2017
New insights into mitral valve dystrophy: a Filamin-A genotype-phenotype and outcome studyThierry Le Tourneau, Solena Le Scouarnec, Caroline Cueff, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Structure (London, England : 1993)|October 23, 2018
Non-syndromic Mitral Valve Dysplasia Mutation Changes the Force Resilience and Interaction of Human Filamin ATatu J K Haataja, Rafael C Bernardi, Simon Lecointe, et al.
Biophysical Journal|September 23, 2019
Critical Structural Defects Explain Filamin A Mutations Causing Mitral Valve DysplasiaTatu J K Haataja, Romain Capoulade, Simon Lecointe, et al.
Journal of Cardiovascular Translational Research|July 21, 2011
Filamin-a-related myxomatous mitral valve dystrophy: genetic, echocardiographic and functional aspectsAurélie Lardeux, Florence Kyndt, Simon Lecointe, et al.
Biochimica Et Biophysica Acta. Molecular Cell Research|March 22, 2017
The alternatively spliced LRRFIP1 Isoform-1 is a key regulator of the Wnt/β-catenin transcription pathwayPauline Labbé, Emilie Faure, Simon Lecointe, et al.
Atherosclerosis|May 16, 2016
Identification of novel APOB mutations by targeted next-generation sequencing for the molecular diagnosis of familial hypobetalipoproteinemiaAntoine Rimbert, Matthieu Pichelin, Simon Lecointe, 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.
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.
Cardiovascular Research|August 24, 2022
Multimodality imaging and transcriptomics to phenotype mitral valve dystrophy in a unique knock-in Filamin-A rat modelConstance Delwarde, Claire Toquet, Pascal Aumond, et al.
Circulation. Genomic and Precision Medicine|March 7, 2020
Genetic Association Analyses Highlight <i>IL6</i>, <i>ALPL</i>, and <i>NAV1</i> As 3 New Susceptibility Genes Underlying Calcific Aortic Valve StenosisSébastien Thériault, Christian Dina, David Messika-Zeitoun, et al.
European Heart Journal|October 12, 2017
New insights into mitral valve dystrophy: a Filamin-A genotype-phenotype and outcome studyThierry Le Tourneau, Solena Le Scouarnec, Caroline Cueff, et al.
Pageof 2