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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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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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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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The N-Terminal Juxtamembranous Domain of KCNQ1 Is Critical for Channel Surface Expression: Implications in the Romano-Ward LQT1 Syndrome

Circulation research, 2006-11, Vol.99 (10), p.1076-1083

2006

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Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease

Journal of the American College of Cardiology, 2003-02, Vol.41 (4), p.643-652

2003

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Microarray Analysis Reveals Complex Remodeling of Cardiac Ion Channel Expression With Altered Thyroid Status: Relation to Cellular and Integrated Electrophysiology

Circulation research, 2003-02, Vol.92 (2), p.234-242

2003

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Multifocal Ectopic Purkinje-Related Premature Contractions: A New SCN5A-Related Cardiac Channelopathy

Journal of the American College of Cardiology, 2012-07, Vol.60 (2), p.144-156

2012

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The KCNQ1 potassium channel is down-regulated by ubiquitylating enzymes of the Nedd4/Nedd4-like family

Cardiovascular research, 2007-04, Vol.74 (1), p.64-74

2007

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Mutations in a Dominant-Negative Isoform Correlate with Phenotype in Inherited Cardiac Arrhythmias

American journal of human genetics, 1999-04, Vol.64 (4), p.1015-1023

1999

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IKs response to protein kinase A-dependent KCNQ1 phosphorylation requires direct interaction with microtubules

Cardiovascular research, 2008-08, Vol.79 (3), p.427-435

2008

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New KCNQ1 mutations leading to haploinsufficiency in a general population: Defective trafficking of a KvLQT1 mutant

Cardiovascular research, 2004-07, Vol.63 (1), p.60-68

2004

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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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Effects of sulphonylureas on cAMP-stimulated Cl- transport via the cystic fibrosis gene product in human epithelial cells

Pflügers Archiv, 1994-02, Vol.426 (3-4), p.284-287

1994

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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.49 (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.47 (6), p.H1908-H1915

2000

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Non-invasive testing of acquired long QT syndrome: Evidence for multiple arrhythmogenic substrates: Spotlight issue on sudden cardiac death

Cardiovascular research, 2001, Vol.50 (2), p.386-398

2001

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Transgenic mice overexpressing human KvLQT1 dominant-negative isoform: Part I : Phenotypic characterisation: Spotlight issue on sudden cardiac death

Cardiovascular research, 2001, Vol.50 (2), p.314-327

2001

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Expression of CFTR controls cAMP-dependent activation of epithelial K+ currents

American Journal of Physiology: Cell Physiology, 1996-11, Vol.40 (5), p.C1565-C1573

1996

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Barium- and calcium-permeable channels open at negative membrane potentials in rat ventricular myocytes

The Journal of membrane biology, 1989-10, Vol.111 (1), p.57-67

1989

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A randomized, controlled trial of computer-assisted cognitive remediation for schizophrenia

Schizophrenia research, 2011-02, Vol.125 (2), p.284-290

2011

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

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

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

The N-Terminal Juxtamembranous Domain of KCNQ1 Is Critical for Channel Surface Expression: Implications in the Romano-Ward LQT1 Syndrome

Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease

Microarray Analysis Reveals Complex Remodeling of Cardiac Ion Channel Expression With Altered Thyroid Status: Relation to Cellular and Integrated Electrophysiology

Multifocal Ectopic Purkinje-Related Premature Contractions: A New SCN5A-Related Cardiac Channelopathy

The KCNQ1 potassium channel is down-regulated by ubiquitylating enzymes of the Nedd4/Nedd4-like family

Mutations in a Dominant-Negative Isoform Correlate with Phenotype in Inherited Cardiac Arrhythmias

IKs response to protein kinase A-dependent KCNQ1 phosphorylation requires direct interaction with microtubules

New KCNQ1 mutations leading to haploinsufficiency in a general population: Defective trafficking of a KvLQT1 mutant

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

Effects of sulphonylureas on cAMP-stimulated Cl- transport via the cystic fibrosis gene product in human epithelial cells

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

Differential expression of KvLQT1 isoforms across the human ventricular wall

Non-invasive testing of acquired long QT syndrome: Evidence for multiple arrhythmogenic substrates: Spotlight issue on sudden cardiac death

Transgenic mice overexpressing human KvLQT1 dominant-negative isoform: Part I : Phenotypic characterisation: Spotlight issue on sudden cardiac death

Expression of CFTR controls cAMP-dependent activation of epithelial K+ currents

Barium- and calcium-permeable channels open at negative membrane potentials in rat ventricular myocytes

A randomized, controlled trial of computer-assisted cognitive remediation for schizophrenia

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