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Regional and tissue specific transcript signatures of ion channel genes in the non-diseased human heart

The Journal of physiology, 2007-07, Vol.582 (2), p.675-693

2007

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Specific pattern of ionic channel gene expression associated with pacemaker activity in the mouse heart

The Journal of physiology, 2005-01, Vol.562 (1), p.223-234

2005

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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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Progressive Cardiac Conduction Defect is the Prevailing Phenotype in Carriers of a Brugada Syndrome SCN5A Mutation

Journal of cardiovascular electrophysiology, 2006-03, Vol.17 (3), p.270-275

2006

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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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Novel Brugada SCN5A Mutation Leading to ST Segment Elevation in the Inferior or the Right Precordial Leads

Journal of cardiovascular electrophysiology, 2003-02, Vol.14 (2), p.200-203

2003

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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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Regional and tissue specific transcript signatures of ion channel genes in the non-diseased human heart

Specific pattern of ionic channel gene expression associated with pacemaker activity in the mouse heart

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

Progressive Cardiac Conduction Defect is the Prevailing Phenotype in Carriers of a Brugada Syndrome SCN5A Mutation

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

Novel Brugada SCN5A Mutation Leading to ST Segment Elevation in the Inferior or the Right Precordial Leads

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

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