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Alexandre Janin

Showing results (1-10 of 43) with videos related to

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Frontiers in Physiology|September 25, 2018
Nesprins and Lamins in Health and Diseases of Cardiac and Skeletal MusclesAlexandre Janin, Vincent Gache
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 22, 2015
A fast and cost-effective molecular diagnostic tool for genetic diseases involved in sudden cardiac deathValérie Chanavat, Alexandre Janin, Gilles Millat
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|March 27, 2018
Cardiac voltage-gated sodium channel mutations associated with left atrial dysfunction and stroke in childrenAdrien Moreau, Alexandre Janin, Gilles Millat, et al.
Molecular Diagnosis & Therapy|March 18, 2018
A Novel Missense Mutation p.Gly162Glu of the Gene MYL2 Involved in Hypertrophic Cardiomyopathy: A Pedigree Analysis of a ProbandPauline Renaudin, Alexandre Janin, Gilles Millat, et al.
Methods in Molecular Biology (Clifton, N.J.)|July 23, 2025
Functional Evaluation of Splice Variants Using a Minigene StrategyAngélique Nizou, Lana Mahfoud, Alexandre Janin, et al.
Nature Geoscience|October 13, 2025
Geodynamics of a global plate reorganization from topological data analysisAlexandre Janin, Nicolas Coltice, Nicolas Chamot-Rooke, et al.
Orphanet Journal of Rare Diseases|September 1, 2017
Nuclear envelopathies: a complex LINC between nuclear envelope and pathologyAlexandre Janin, Delphine Bauer, Francesca Ratti, et al.
Gene|July 18, 2018
First identification of homozygous truncating CSRP3 variants in two unrelated cases with hypertrophic cardiomyopathyAlexandre Janin, Francis Bessière, Samuel Chauveau, et al.
European Journal of Medical Genetics|July 25, 2015
HCN4 mutation as a molecular explanation on patients with bradycardia and non-compaction cardiomyopathyGilles Millat, Alexandre Janin, Olivier de Tauriac, et al.
Molecular Diagnosis & Therapy|May 6, 2021
Molecular Diagnosis of Inherited Cardiac Diseases in the Era of Next-Generation Sequencing: A Single Center's Experience Over 5 YearsAlexandre Janin, Louis Januel, Cécile Cazeneuve, et al.
Pageof 5

Showing results (1-10 of 43) with videos related to

Sort By:
Pageof 5
Frontiers in Physiology|September 25, 2018
Nesprins and Lamins in Health and Diseases of Cardiac and Skeletal MusclesAlexandre Janin, Vincent Gache
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 22, 2015
A fast and cost-effective molecular diagnostic tool for genetic diseases involved in sudden cardiac deathValérie Chanavat, Alexandre Janin, Gilles Millat
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|March 27, 2018
Cardiac voltage-gated sodium channel mutations associated with left atrial dysfunction and stroke in childrenAdrien Moreau, Alexandre Janin, Gilles Millat, et al.
Molecular Diagnosis & Therapy|March 18, 2018
A Novel Missense Mutation p.Gly162Glu of the Gene MYL2 Involved in Hypertrophic Cardiomyopathy: A Pedigree Analysis of a ProbandPauline Renaudin, Alexandre Janin, Gilles Millat, et al.
Methods in Molecular Biology (Clifton, N.J.)|July 23, 2025
Functional Evaluation of Splice Variants Using a Minigene StrategyAngélique Nizou, Lana Mahfoud, Alexandre Janin, et al.
Nature Geoscience|October 13, 2025
Geodynamics of a global plate reorganization from topological data analysisAlexandre Janin, Nicolas Coltice, Nicolas Chamot-Rooke, et al.
Orphanet Journal of Rare Diseases|September 1, 2017
Nuclear envelopathies: a complex LINC between nuclear envelope and pathologyAlexandre Janin, Delphine Bauer, Francesca Ratti, et al.
Gene|July 18, 2018
First identification of homozygous truncating CSRP3 variants in two unrelated cases with hypertrophic cardiomyopathyAlexandre Janin, Francis Bessière, Samuel Chauveau, et al.
European Journal of Medical Genetics|July 25, 2015
HCN4 mutation as a molecular explanation on patients with bradycardia and non-compaction cardiomyopathyGilles Millat, Alexandre Janin, Olivier de Tauriac, et al.
Molecular Diagnosis & Therapy|May 6, 2021
Molecular Diagnosis of Inherited Cardiac Diseases in the Era of Next-Generation Sequencing: A Single Center's Experience Over 5 YearsAlexandre Janin, Louis Januel, Cécile Cazeneuve, et al.
Pageof 5