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Gilles Millat

Showing results (1-10 of 58) with videos related to

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Biochimica Et Biophysica Acta|October 7, 2004
Structure and function of the NPC2 proteinMarie T Vanier, Gilles Millat
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
Molecular Diagnosis & Therapy|April 2, 2014
Evaluation of a new high-throughput next-generation sequencing method based on a custom AmpliSeq™ library and ion torrent PGM™ sequencing for the rapid detection of genetic variations in long QT syndromeGilles Millat, Valérie Chanavat, Robert Rousson
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 12, 2014
Evaluation of a new NGS method based on a custom AmpliSeq library and Ion Torrent PGM sequencing for the fast detection of genetic variations in cardiomyopathiesGilles Millat, Valérie Chanavat, Robert Rousson
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 2010
Development of a high resolution melting method for the detection of genetic variations in hypertrophic cardiomyopathyGilles Millat, Valérie Chanavat, Hervé Créhalet, et al.
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.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 21, 2010
Development of a high resolution melting method for the detection of genetic variations in Long QT SyndromeGilles Millat, Valérie Chanavat, Hervé Créhalet, et al.
Clinical Biochemistry|November 26, 2008
Rapid, sensitive and inexpensive detection of SCN5A genetic variations by high resolution melting analysisGilles Millat, Valérie Chanavat, Claire Rodriguez-Lafrasse, et al.
DNA and Cell Biology|April 8, 2015
Functional characterization of putative novel splicing mutations in the cardiomyopathy-causing genesGilles Millat, Estèle Lafont, Séverine Nony, et al.
Pageof 6

Showing results (1-10 of 58) with videos related to

Sort By:
Pageof 6
Biochimica Et Biophysica Acta|October 7, 2004
Structure and function of the NPC2 proteinMarie T Vanier, Gilles Millat
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
Molecular Diagnosis & Therapy|April 2, 2014
Evaluation of a new high-throughput next-generation sequencing method based on a custom AmpliSeq™ library and ion torrent PGM™ sequencing for the rapid detection of genetic variations in long QT syndromeGilles Millat, Valérie Chanavat, Robert Rousson
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 12, 2014
Evaluation of a new NGS method based on a custom AmpliSeq library and Ion Torrent PGM sequencing for the fast detection of genetic variations in cardiomyopathiesGilles Millat, Valérie Chanavat, Robert Rousson
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 2010
Development of a high resolution melting method for the detection of genetic variations in hypertrophic cardiomyopathyGilles Millat, Valérie Chanavat, Hervé Créhalet, et al.
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.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 21, 2010
Development of a high resolution melting method for the detection of genetic variations in Long QT SyndromeGilles Millat, Valérie Chanavat, Hervé Créhalet, et al.
Clinical Biochemistry|November 26, 2008
Rapid, sensitive and inexpensive detection of SCN5A genetic variations by high resolution melting analysisGilles Millat, Valérie Chanavat, Claire Rodriguez-Lafrasse, et al.
DNA and Cell Biology|April 8, 2015
Functional characterization of putative novel splicing mutations in the cardiomyopathy-causing genesGilles Millat, Estèle Lafont, Séverine Nony, et al.
Pageof 6