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Modelling sudden cardiac death risks factors in patients with coronavirus disease of 2019: the hydroxychloroquine and azithromycin case

Europace (London, England), 2021-05, Vol.23 (7), p.1124-1136

2021

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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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Gap-134, a Connexin43 activator, prevents age-related development of ventricular fibrosis in Scn5a+/− mice

Pharmacological research, 2020-09, Vol.159, p.104922-104922, Article 104922

2020

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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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Transforming growth factor β receptor inhibition prevents ventricular fibrosis in a mouse model of progressive cardiac conduction disease

Cardiovascular research, 2017-04, Vol.113 (5), p.464-474

2017

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Marine n-3 PUFAs modulate IKs gating, channel expression, and location in membrane microdomains

Cardiovascular research, 2015-02, Vol.105 (2), p.223-232

2015

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Kv7.1 (KCNQ1) properties and channelopathies

The Journal of physiology, 2008-04, Vol.586 (7), p.1785-1789

2008

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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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KCNE1–KCNQ1 osmoregulation by interaction of phosphatidylinositol‐4,5‐bisphosphate with Mg2+ and polyamines

The Journal of physiology, 2010-09, Vol.588 (18), p.3471-3483

2010

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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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Atrial fibrillation: Is NO an answer for refractoriness?

Cardiovascular research, 2006-10, Vol.72 (1), p.7-8

BARO, I

2006

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Infanticide vs. inherited cardiac arrhythmias

Europace (London, England), 2021-03, Vol.23 (3), p.441-450

2021

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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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Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations

Basic research in cardiology, 2014-11, Vol.109 (6), p.446-446, Article 446

2014

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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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KCNE1-KCNQ1 osmoregulation by interaction of phosphatidylinositol-4,5-bisphosphate with Mg 2+ and polyamines: Mechanism of KCNE1-KCNQ1 osmoregulation

The Journal of physiology, 2010-09, Vol.588 (18), p.3471-3483

2010

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I Ks 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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Non-invasive testing of acquired long QT syndrome: evidence for multiple arrhythmogenic substrates

Cardiovascular research, 2001-05, Vol.50 (2), p.386-398

2001

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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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Abstract 1507: Disruption of KCNH2 Trafficking May Contribute to Severe Clinical Phenotype of Trafficking Deficient Long-QT Type-1 Mutation KCNQ1-T587M

Circulation (New York, N.Y.), 2008-10, Vol.118 (suppl_18)

2008

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Transgenic mice overexpressing human KvLQT1 dominant-negative isoform. Part I: Phenotypic characterisation

Cardiovascular research, 2001-05, Vol.50 (2), p.314-327

2001

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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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Modelling sudden cardiac death risks factors in patients with coronavirus disease of 2019: the hydroxychloroquine and azithromycin case

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

Gap-134, a Connexin43 activator, prevents age-related development of ventricular fibrosis in Scn5a+/− mice

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

Transforming growth factor β receptor inhibition prevents ventricular fibrosis in a mouse model of progressive cardiac conduction disease

Marine n-3 PUFAs modulate IKs gating, channel expression, and location in membrane microdomains

Kv7.1 (KCNQ1) properties and channelopathies

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

KCNE1–KCNQ1 osmoregulation by interaction of phosphatidylinositol‐4,5‐bisphosphate with Mg2+ and polyamines

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

Atrial fibrillation: Is NO an answer for refractoriness?

RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome

Infanticide vs. inherited cardiac arrhythmias

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

Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations

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

KCNE1-KCNQ1 osmoregulation by interaction of phosphatidylinositol-4,5-bisphosphate with Mg 2+ and polyamines: Mechanism of KCNE1-KCNQ1 osmoregulation

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

Non-invasive testing of acquired long QT syndrome: evidence for multiple arrhythmogenic substrates

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

Abstract 1507: Disruption of KCNH2 Trafficking May Contribute to Severe Clinical Phenotype of Trafficking Deficient Long-QT Type-1 Mutation KCNQ1-T587M

Transgenic mice overexpressing human KvLQT1 dominant-negative isoform. Part I: Phenotypic characterisation

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

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