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The Cherenkov Telescope Array production system for Monte Carlo simulations and analysis

Journal of Physics: Conference Series, 2017-10, Vol.898 (5), p.52013

2017

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Study of the cardiac sodium channel in a mouse model of Scn5a haploinsufficiency towards a novel approach of therapy

Cardiovascular research, 2024-05, Vol.120 (Supplement_1)

2024

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Notched T waves on Holter recordings enhance detection of patients with LQT2 (HERG) mutations

Circulation (New York, N.Y.), 2001-02, Vol.103 (8), p.1095-1101

2001

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Different Atrial and Ventricular Resting Membrane Potentials May Explain the Phenotypical Variability of a Truncating SCN5A Mutation

Heart rhythm, 2013-11, Vol.10 (11), p.1746-1746

2013

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Dominant-Negative Suppression of Nav1.5 Channel by N-Terminal SCN5A Mutations in Brugada Syndrome

Heart rhythm, 2011, Vol.8 (11), p.1824-1824

2011

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Diagnostic performance of QT interval variables from 24-h electrocardiography in the long QT syndrome

European heart journal, 1998-01, Vol.19 (1), p.158-165

1998

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Syndrome du QT long congénital

La Presse médicale (1983), 1998-06, Vol.27 (21), p.1029-1034

1998

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P5713A new scn5a mutation responsible for multifocal ectopic purkinje-related premature contractions

European heart journal, 2018-08, Vol.39 (suppl_1)

2018

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279Exploration of the dominant-negative effect of a SCN5A mutation in mice using adeno-associated viruses

Cardiovascular research, 2016-07, Vol.111 (suppl 1), p.S54-S54

2016

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P128Recovery of Scn5a-deficient mice cardiac conduction using AAVs

Cardiovascular research, 2018-04, Vol.114 (suppl_1), p.S33-S33

2018

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A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

Nature genetics, 1997-02, Vol.15 (2), p.186-189

1997

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Splicing mutations in KCNQ1 : A mutation hot spot at codon 344 that produces in frame transcripts

Circulation (New York, N.Y.), 1999-09, Vol.100 (10), p.1077-1084

1999

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CRISPR/Cas9-mediated generation of cardiomyocytes derived from human induced pluripotent stem cells to model SCN5A deficiency

Archives of Cardiovascular Diseases Supplements, 2021-05, Vol.13 (2), p.232-233

2021

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P371Role of the N- and distal C-terminal domains in Nav1.5 alpha-subunit interaction

Cardiovascular research, 2014-07, Vol.103 (suppl 1), p.S68-S68

2014

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Isoform-Specific Modulation of Voltage-Gated Na+ Channels by Calmodulin

Circulation research, 2002-03, Vol.90 (4), p.e49-e57

2002

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KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome

Circulation (New York, N.Y.), 1997-11, Vol.96 (9), p.2778-2781

1997

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Somatic gene transfer of tagged K+ channel fragments to probe trafficking and electrical function in epithelial cells and cardiac myocytes

The Journal of membrane biology, 2002-11, Vol.190 (2), p.133-144

2002

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Overexpression of the cardiac Na + channel in Scn5a deficient mice using AAVs

Archives of cardiovascular diseases supplements, 2017-04, Vol.9 (2), p.169

2017

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227 - Overexpression of the cardiac Na+ channel in Scn5a deficient mice using AAVs

Archives of Cardiovascular Diseases Supplements, 2017-04, Vol.9 (2), p.169-169

2017

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Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias

The EMBO journal, 1997-09, Vol.16 (17), p.5472-5479

1997

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Genomic Organization of the KCNQ1 K+ Channel Gene and Identification of C-Terminal Mutations in the Long-QT Syndrome

Circulation research, 1999-02, Vol.84 (3), p.290-297

1999

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Heart rate influences on repolarization duration and morphology in symptomatic versus asymptomatic KCNQ1 mutation carriers

The American journal of cardiology, 2005-02, Vol.95 (3), p.406-409

2005

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Syndrome du QT long congénital: apport de la génétique dans l'évaluation pronostique

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 1999, Vol.6, p.S519-S519

1999

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Different circadian behavior of the apex and the end of the T wave

Journal of electrocardiology, 1995, Vol.28, p.138-142

1995

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The Cherenkov Telescope Array production system for Monte Carlo simulations and analysis

Study of the cardiac sodium channel in a mouse model of Scn5a haploinsufficiency towards a novel approach of therapy

Notched T waves on Holter recordings enhance detection of patients with LQT2 (HERG) mutations

Different Atrial and Ventricular Resting Membrane Potentials May Explain the Phenotypical Variability of a Truncating SCN5A Mutation

Dominant-Negative Suppression of Nav1.5 Channel by N-Terminal SCN5A Mutations in Brugada Syndrome

Diagnostic performance of QT interval variables from 24-h electrocardiography in the long QT syndrome

Syndrome du QT long congénital

P5713A new scn5a mutation responsible for multifocal ectopic purkinje-related premature contractions

279Exploration of the dominant-negative effect of a SCN5A mutation in mice using adeno-associated viruses

P128Recovery of Scn5a-deficient mice cardiac conduction using AAVs

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

Splicing mutations in KCNQ1 : A mutation hot spot at codon 344 that produces in frame transcripts

CRISPR/Cas9-mediated generation of cardiomyocytes derived from human induced pluripotent stem cells to model SCN5A deficiency

P371Role of the N- and distal C-terminal domains in Nav1.5 alpha-subunit interaction

Isoform-Specific Modulation of Voltage-Gated Na+ Channels by Calmodulin

KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome

Somatic gene transfer of tagged K+ channel fragments to probe trafficking and electrical function in epithelial cells and cardiac myocytes

Overexpression of the cardiac Na + channel in Scn5a deficient mice using AAVs

227 - Overexpression of the cardiac Na+ channel in Scn5a deficient mice using AAVs

Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias

Genomic Organization of the KCNQ1 K+ Channel Gene and Identification of C-Terminal Mutations in the Long-QT Syndrome

Heart rate influences on repolarization duration and morphology in symptomatic versus asymptomatic KCNQ1 mutation carriers

Syndrome du QT long congénital: apport de la génétique dans l'évaluation pronostique

Different circadian behavior of the apex and the end of the T wave

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