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Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non–SCN5A-related patients

Journal of the American College of Cardiology, 2002-07, Vol.40 (2), p.350-356

2002

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Polyethylenimine but Not Cationic Lipids Promotes Transgene Delivery to the Nucleus in Mammalian Cells

The Journal of biological chemistry, 1998-03, Vol.273 (13), p.7507-7511

1998

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Variable Na(v)1.5 protein expression from the wild-type allele correlates with the penetrance of cardiac conduction disease in the Scn5a(+/-) mouse model

PloS one, 2010-02, Vol.5 (2), p.e9298-e9298

2010

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Impaired KCNQ1–KCNE1 and Phosphatidylinositol-4,5-Bisphosphate Interaction Underlies the Long QT Syndrome

Circulation research, 2005-04, Vol.96 (7), p.730-739

2005

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Gastrointestinal prokinetic drugs have different affinity for the human cardiac human ether-à-gogo K(+) channel

The Journal of pharmacology and experimental therapeutics, 2001-12, Vol.299 (3), p.1007

2001

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14-3-3 Is a Regulator of the Cardiac Voltage-Gated Sodium Channel Nav1.5

Circulation research, 2006-06, Vol.98 (12), p.1538-1546

2006

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Differential expression of KvLQT1 and its regulator IsK in mouse epithelia

American Journal of Physiology: Cell Physiology, 2001-02, Vol.280 (2), p.C359-C372

2001

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A Common Antitussive Drug, Clobutinol, Precipitates the Long QT Syndrome 2

Molecular pharmacology, 2004-11, Vol.66 (5), p.1093-1102

2004

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Gender-related differences in ion-channel and transporter subunit expression in non-diseased human hearts

Journal of molecular and cellular cardiology, 2010-10, Vol.49 (4), p.639-646

2010

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Long-term amiodarone administration remodels expression of ion channel transcripts in the mouse heart

Circulation (New York, N.Y.), 2004-11, Vol.110 (19), p.3028-3035

2004

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AKAP proteins anchor cAMP-dependent protein kinase to KvLQT1/IsK channel complex

American journal of physiology. Heart and circulatory physiology, 2001-05, Vol.280 (5), p.H2038-H2045

2001

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Differential expression of KvLQT1 isoforms across the human ventricular wall

American journal of physiology. Heart and circulatory physiology, 2000-06, Vol.278 (6), p.H1908-H1915

2000

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Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans

The Journal of clinical investigation, 2008-06, Vol.118 (6), p.2260-2268

2008

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K + channel openers and ‘natural’ cardioprotection

Trends in pharmacological sciences (Regular ed.), 1992, Vol.13 (7), p.269-272

1992

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Mutation in the KCNQ1 gene leading to the short QT-interval syndrome

Circulation (New York, N.Y.), 2004-05, Vol.109 (20), p.2394-2397

2004

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A Dominant Negative Isoform of the Long QT Syndrome 1 Gene Product

The Journal of biological chemistry, 1998-03, Vol.273 (12), p.6837-6843

1998

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Human atrial ion channel and transporter subunit gene-expression remodeling associated with valvular heart disease and atrial fibrillation

Circulation (New York, N.Y.), 2005-07, Vol.112 (4), p.471-481

2005

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Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

Nature (London), 2003-02, Vol.421 (6923), p.634-639

2003

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Bradycardia and Slowing of the Atrioventricular Conduction in Mice Lacking CaV3.1/α1G T-Type Calcium Channels

Circulation research, 2006-06, Vol.98 (11), p.1422-1430

2006

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β3-Adrenoceptor Control the Cystic Fibrosis Transmembrane Conductance Regulator through a cAMP/Protein Kinase A-independent Pathway

The Journal of biological chemistry, 1999-03, Vol.274 (10), p.6107-6113

1999

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In vitro molecular interactions and distribution of KCNE family with KCNQ1 in the human heart

Cardiovascular research, 2005-08, Vol.67 (3), p.529-538

2005

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Defining the cellular phenotype of ankyrin-B syndrome variants : Human ANK2 variants associated with clinical phenotypes display a spectrum of activities in cardiomyocytes

Circulation (New York, N.Y.), 2007-01, Vol.115 (4), p.432-441

2007

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Pharmacogenetics of cardiac K + channels

European journal of pharmacology, 2000-12, Vol.410 (2), p.281-287

Escande, Denis

2000

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Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large french family

Circulation (New York, N.Y.), 2001-12, Vol.104 (25), p.3081-3086

2001

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Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non–SCN5A-related patients

Polyethylenimine but Not Cationic Lipids Promotes Transgene Delivery to the Nucleus in Mammalian Cells

Variable Na(v)1.5 protein expression from the wild-type allele correlates with the penetrance of cardiac conduction disease in the Scn5a(+/-) mouse model

Variable Nav1.5 Protein Expression from the Wild-Type Allele Correlates with the Penetrance of Cardiac Conduction Disease in the Scn5a+/− Mouse Model

Impaired KCNQ1–KCNE1 and Phosphatidylinositol-4,5-Bisphosphate Interaction Underlies the Long QT Syndrome

Gastrointestinal prokinetic drugs have different affinity for the human cardiac human ether-à-gogo K(+) channel

14-3-3 Is a Regulator of the Cardiac Voltage-Gated Sodium Channel Nav1.5

Differential expression of KvLQT1 and its regulator IsK in mouse epithelia

A Common Antitussive Drug, Clobutinol, Precipitates the Long QT Syndrome 2

Gender-related differences in ion-channel and transporter subunit expression in non-diseased human hearts

Long-term amiodarone administration remodels expression of ion channel transcripts in the mouse heart

AKAP proteins anchor cAMP-dependent protein kinase to KvLQT1/IsK channel complex

Differential expression of KvLQT1 isoforms across the human ventricular wall

Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans

K + channel openers and ‘natural’ cardioprotection

Mutation in the KCNQ1 gene leading to the short QT-interval syndrome

A Dominant Negative Isoform of the Long QT Syndrome 1 Gene Product

Human atrial ion channel and transporter subunit gene-expression remodeling associated with valvular heart disease and atrial fibrillation

Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

Bradycardia and Slowing of the Atrioventricular Conduction in Mice Lacking CaV3.1/α1G T-Type Calcium Channels

β3-Adrenoceptor Control the Cystic Fibrosis Transmembrane Conductance Regulator through a cAMP/Protein Kinase A-independent Pathway

In vitro molecular interactions and distribution of KCNE family with KCNQ1 in the human heart

Defining the cellular phenotype of ankyrin-B syndrome variants : Human ANK2 variants associated with clinical phenotypes display a spectrum of activities in cardiomyocytes

Pharmacogenetics of cardiac K + channels

Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large french family

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