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Solena Le Scouarnec

Showing results (11-20 of 39) with videos related to

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Frontiers in Cardiovascular Medicine|March 6, 2023
Genetics and pathophysiology of mitral valve prolapseConstance Delwarde, Romain Capoulade, Jean Mérot, et al.
Journal of the American College of Cardiology|January 1, 2013
Identification of large families in early repolarization syndromeJean-Baptiste Gourraud, Solena Le Scouarnec, Frederic Sacher, et al.
Circulation|January 24, 2007
Defining the cellular phenotype of "ankyrin-B syndrome" variants: human ANK2 variants associated with clinical phenotypes display a spectrum of activities in cardiomyocytesPeter J Mohler, Solena Le Scouarnec, Isabelle Denjoy, et al.
International Journal of Cardiology|April 15, 2022
Heritability of aortic valve stenosis and bicuspid enrichment in families with aortic valve stenosisAnne-Sophie Boureau, Matilde Karakachoff, Solena Le Scouarnec, et al.
Nature Communications|March 21, 2023
Variations in the poly-histidine repeat motif of HOXA1 contribute to bicuspid aortic valve in mouse and zebrafishGaëlle Odelin, Adèle Faucherre, Damien Marchese, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 4, 2008
Dysfunction in ankyrin-B-dependent ion channel and transporter targeting causes human sinus node diseaseSolena Le Scouarnec, Naina Bhasin, Claude Vieyres, et al.
Cardiovascular Research|June 23, 2026
Macrophage recruitment is a hallmark of non-syndromic myxomatous mitral valve diseaseBenjamin Le Vely, Constance Delwarde, Claire Toquet, et al.
Heart (British Cardiac Society)|December 26, 2023
Filamin A heart valve disease as a genetic cause of inherited bicuspid and tricuspid aortic valve diseaseConstance Delwarde, Claire Toquet, Anne Sophie Boureau, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndromeVincent Probst, Arthur A M Wilde, Julien Barc, et al.
Plos One|February 23, 2010
Variable Na(v)1.5 protein expression from the wild-type allele correlates with the penetrance of cardiac conduction disease in the Scn5a(+/-) mouse modelAnne-Laure Leoni, Bruno Gavillet, Jean-Sébastien Rougier, et al.
Pageof 4

Showing results (11-20 of 39) with videos related to

Sort By:
Pageof 4
Frontiers in Cardiovascular Medicine|March 6, 2023
Genetics and pathophysiology of mitral valve prolapseConstance Delwarde, Romain Capoulade, Jean Mérot, et al.
Journal of the American College of Cardiology|January 1, 2013
Identification of large families in early repolarization syndromeJean-Baptiste Gourraud, Solena Le Scouarnec, Frederic Sacher, et al.
Circulation|January 24, 2007
Defining the cellular phenotype of "ankyrin-B syndrome" variants: human ANK2 variants associated with clinical phenotypes display a spectrum of activities in cardiomyocytesPeter J Mohler, Solena Le Scouarnec, Isabelle Denjoy, et al.
International Journal of Cardiology|April 15, 2022
Heritability of aortic valve stenosis and bicuspid enrichment in families with aortic valve stenosisAnne-Sophie Boureau, Matilde Karakachoff, Solena Le Scouarnec, et al.
Nature Communications|March 21, 2023
Variations in the poly-histidine repeat motif of HOXA1 contribute to bicuspid aortic valve in mouse and zebrafishGaëlle Odelin, Adèle Faucherre, Damien Marchese, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 4, 2008
Dysfunction in ankyrin-B-dependent ion channel and transporter targeting causes human sinus node diseaseSolena Le Scouarnec, Naina Bhasin, Claude Vieyres, et al.
Cardiovascular Research|June 23, 2026
Macrophage recruitment is a hallmark of non-syndromic myxomatous mitral valve diseaseBenjamin Le Vely, Constance Delwarde, Claire Toquet, et al.
Heart (British Cardiac Society)|December 26, 2023
Filamin A heart valve disease as a genetic cause of inherited bicuspid and tricuspid aortic valve diseaseConstance Delwarde, Claire Toquet, Anne Sophie Boureau, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndromeVincent Probst, Arthur A M Wilde, Julien Barc, et al.
Plos One|February 23, 2010
Variable Na(v)1.5 protein expression from the wild-type allele correlates with the penetrance of cardiac conduction disease in the Scn5a(+/-) mouse modelAnne-Laure Leoni, Bruno Gavillet, Jean-Sébastien Rougier, et al.
Pageof 4