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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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Delayed rectifier K+ currents and cardiac repolarization

Journal of molecular and cellular cardiology, 2010-01, Vol.48 (1), p.37-44

2010

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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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Dual Effect of Phosphatidyl (4,5)-Bisphosphate PIP2 on Shaker K+ Channels

The Journal of biological chemistry, 2012-10, Vol.287 (43), p.36158-36167

2012

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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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Kv7.1 (KCNQ1) properties and channelopathies

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

2008

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Phosphatidylinositol-4,5-Bisphosphate (PIP2) Stabilizes the Open Pore Conformation of the Kv11.1 (hERG) Channel

Biophysical journal, 2010-08, Vol.99 (4), p.1110-1118

2010

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LQT1-associated Mutations Increase KCNQ1 Proteasomal Degradation Independently of Derlin-1

The Journal of biological chemistry, 2009-02, Vol.284 (8), p.5250-5256

2009

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Mouse Models of SCN5A-Related Cardiac Arrhythmias

Frontiers in physiology, 2012-01, Vol.3, p.210-210

2012

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Neural modulation of ion channels in cardiac arrhythmias: Clinical implications and future investigations

Heart rhythm, 2010-06, Vol.7 (6), p.847-849

2010

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Dysfunction of the Voltage‐Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome

Journal of the American Heart Association, 2016-06, Vol.5 (6), p.n/a

2016

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Dual effect of phosphatidylinositol (4,5)-bisphosphate PIP2 on Shaker K+ channels

The Journal of biological chemistry, 2013-04, Vol.288 (15), p.10951-10951

2013

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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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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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Trafficking-deficient long QT syndrome mutation KCNQ1-T587M confers severe clinical phenotype by impairment of KCNH2 membrane localization: Evidence for clinically significant I Kr-I Ks α-subunit interaction

Heart rhythm, 2009-12, Vol.6 (12), p.1792-1801

2009

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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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Trafficking-deficient long QT syndrome mutation KCNQ1-T587M confers severe clinical phenotype by impairment of KCNH2 membrane localization: Evidence for clinically significant IKr -IKs α-subunit interaction

Heart rhythm, 2009-12, Vol.6 (12), p.1792-1801

2009

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sigma(2)-receptor ligand-mediated inhibition of inwardly rectifying K(+) channels in the heart

The Journal of pharmacology and experimental therapeutics, 2007-07, Vol.322 (1), p.341

2007

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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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Transfer of Rolf S3-S4 Linker to hERG Eliminates Activation Gating but Spares Inactivation

Biophysical journal, 2009-09, Vol.97 (5), p.1323-1334

2009

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

Delayed rectifier K+ currents and cardiac repolarization

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

Dual Effect of Phosphatidyl (4,5)-Bisphosphate PIP2 on Shaker K+ Channels

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

Kv7.1 (KCNQ1) properties and channelopathies

Phosphatidylinositol-4,5-Bisphosphate (PIP2) Stabilizes the Open Pore Conformation of the Kv11.1 (hERG) Channel

LQT1-associated Mutations Increase KCNQ1 Proteasomal Degradation Independently of Derlin-1

Mouse Models of SCN5A-Related Cardiac Arrhythmias

Neural modulation of ion channels in cardiac arrhythmias: Clinical implications and future investigations

Dysfunction of the Voltage‐Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome

Dual effect of phosphatidylinositol (4,5)-bisphosphate PIP2 on Shaker K+ channels

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

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

Trafficking-deficient long QT syndrome mutation KCNQ1-T587M confers severe clinical phenotype by impairment of KCNH2 membrane localization: Evidence for clinically significant I Kr-I Ks α-subunit interaction

Atrial fibrillation: Is NO an answer for refractoriness?

Trafficking-deficient long QT syndrome mutation KCNQ1-T587M confers severe clinical phenotype by impairment of KCNH2 membrane localization: Evidence for clinically significant IKr -IKs α-subunit interaction

sigma(2)-receptor ligand-mediated inhibition of inwardly rectifying K(+) channels in the heart

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

Transfer of Rolf S3-S4 Linker to hERG Eliminates Activation Gating but Spares Inactivation

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

Differential expression of KvLQT1 isoforms across the human ventricular wall

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

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