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Solena Le Scouarnec

Showing results (1-10 of 39) with videos related to

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Bioinformatics (Oxford, England)|October 11, 2011
Knime4Bio: a set of custom nodes for the interpretation of next-generation sequencing data with KNIMEPierre Lindenbaum, Solena Le Scouarnec, Vincent Portero, et al.
Journal of Molecular and Cellular Cardiology|September 16, 2008
Exon organization and novel alternative splicing of the human ANK2 gene: implications for cardiac function and human cardiac diseaseShane R Cunha, Solena Le Scouarnec, Jean-Jacques Schott, et al.
Bioinformatics (Oxford, England)|March 2, 2011
aCGH.Spline--an R package for aCGH dye bias normalizationTomas W Fitzgerald, Lee D Larcombe, Solena Le Scouarnec, et al.
Frontiers in Cardiovascular Medicine|May 21, 2016
The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex InheritanceJean-Baptiste Gourraud, Julien Barc, Aurélie Thollet, et al.
Heart Rhythm|April 29, 2014
Myotonic dystrophy type 1 mimics and exacerbates Brugada phenotype induced by Nav1.5 sodium channel loss-of-function mutationThomas Pambrun, Aurélie Mercier, Aurélien Chatelier, et al.
Heart (British Cardiac Society)|January 21, 2018
Genetics of syndromic and non-syndromic mitral valve prolapseThierry Le Tourneau, Jean Mérot, Antoine Rimbert, et al.
Circulation|February 8, 2006
Familial aggregation of calcific aortic valve stenosis in the western part of FranceVincent Probst, Solena Le Scouarnec, Antoine Legendre, et al.
Plos One|July 26, 2017
DoEstRare: A statistical test to identify local enrichments in rare genomic variants associated with diseaseElodie Persyn, Matilde Karakachoff, Solena Le Scouarnec, 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.
Pageof 4

Showing results (1-10 of 39) with videos related to

Sort By:
Pageof 4
Bioinformatics (Oxford, England)|October 11, 2011
Knime4Bio: a set of custom nodes for the interpretation of next-generation sequencing data with KNIMEPierre Lindenbaum, Solena Le Scouarnec, Vincent Portero, et al.
Journal of Molecular and Cellular Cardiology|September 16, 2008
Exon organization and novel alternative splicing of the human ANK2 gene: implications for cardiac function and human cardiac diseaseShane R Cunha, Solena Le Scouarnec, Jean-Jacques Schott, et al.
Bioinformatics (Oxford, England)|March 2, 2011
aCGH.Spline--an R package for aCGH dye bias normalizationTomas W Fitzgerald, Lee D Larcombe, Solena Le Scouarnec, et al.
Frontiers in Cardiovascular Medicine|May 21, 2016
The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex InheritanceJean-Baptiste Gourraud, Julien Barc, Aurélie Thollet, et al.
Heart Rhythm|April 29, 2014
Myotonic dystrophy type 1 mimics and exacerbates Brugada phenotype induced by Nav1.5 sodium channel loss-of-function mutationThomas Pambrun, Aurélie Mercier, Aurélien Chatelier, et al.
Heart (British Cardiac Society)|January 21, 2018
Genetics of syndromic and non-syndromic mitral valve prolapseThierry Le Tourneau, Jean Mérot, Antoine Rimbert, et al.
Circulation|February 8, 2006
Familial aggregation of calcific aortic valve stenosis in the western part of FranceVincent Probst, Solena Le Scouarnec, Antoine Legendre, et al.
Plos One|July 26, 2017
DoEstRare: A statistical test to identify local enrichments in rare genomic variants associated with diseaseElodie Persyn, Matilde Karakachoff, Solena Le Scouarnec, 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.
Pageof 4