hiPSC-derived cardiomyocytes from Brugada Syndrome patients without identified mutations do not exhibit clear cellular electrophysiological abnormalities (Q37148058)

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scientific article published on 03 August 2016

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English	hiPSC-derived cardiomyocytes from Brugada Syndrome patients without identified mutations do not exhibit clear cellular electrophysiological abnormalities	scientific article published on 03 August 2016

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20 March 2020

hiPSC-derived cardiomyocytes from Brugada Syndrome patients without identified mutations do not exhibit clear cellular electrophysiological abnormalities (English)

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20 March 2020

electrophysiology

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Brugada syndrome

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5

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20 March 2020

Arie O. Verkerk

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20 March 2020

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Arthur A M Wilde

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20 March 2020

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Christiaan C Veerman

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20 March 2020

Isabella Mengarelli

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20 March 2020

Kaomei Guan

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20 March 2020

Michael Stauske

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20 March 2020

Hanno L Tan

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20 March 2020

Connie R Bezzina

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20 March 2020

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3 August 2016

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20 March 2020

Scientific Reports

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20 March 2020

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20 March 2020

30967

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20 March 2020

Fibrosis, Connexin-43, and Conduction Abnormalities in the Brugada Syndrome.

1 reference

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6 September 2017

Cardiac electrophysiological substrate underlying the ECG phenotype and electrogram abnormalities in Brugada syndrome patients

1 reference

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6 September 2017

Ion channelopathies in human induced pluripotent stem cell derived cardiomyocytes: a dynamic clamp study with virtual IK1.

1 reference

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Immaturity of human stem-cell-derived cardiomyocytes in culture: fatal flaw or soluble problem?

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Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

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Identification and characterization of a transient outward K+ current in human induced pluripotent stem cell-derived cardiomyocytes.

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Induced pluripotent stem cell derived cardiomyocytes as models for cardiac arrhythmias

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Spectrum and prevalence of mutations involving BrS1- through BrS12-susceptibility genes in a cohort of unrelated patients referred for Brugada syndrome genetic testing: implications for genetic testing.

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6 September 2017

Cardiomyocytes derived from pluripotent stem cells recapitulate electrophysiological characteristics of an overlap syndrome of cardiac sodium channel disease

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Knime4Bio: a set of custom nodes for the interpretation of next-generation sequencing data with KNIME.

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Re-evaluation of the action potential upstroke velocity as a measure of the Na+ current in cardiac myocytes at physiological conditions

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6 September 2017

SAP97 and dystrophin macromolecular complexes determine two pools of cardiac sodium channels Nav1.5 in cardiomyocytes

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6 September 2017

Patient-specific induced pluripotent stem-cell models for long-QT syndrome

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6 September 2017

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6 September 2017

The Brugada ECG pattern: a marker of channelopathy, structural heart disease, or neither? Toward a unifying mechanism of the Brugada syndrome.

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6 September 2017

Drugs and Brugada syndrome patients: review of the literature, recommendations, and an up-to-date website (www.brugadadrugs.org)

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6 September 2017

The Sequence Alignment/Map format and SAMtools

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6 September 2017

Fast and accurate short read alignment with Burrows-Wheeler transform

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Human Splicing Finder: an online bioinformatics tool to predict splicing signals

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6 September 2017

Developmental basis for electrophysiological heterogeneity in the ventricular and outflow tract myocardium as a substrate for life-threatening ventricular arrhythmias

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Characterization and prediction of alternative splice sites

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Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association.

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A single Na(+) channel mutation causing both long-QT and Brugada syndromes

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Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome

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Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiological, genetic, histopathologic, and computational study.

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High prevalence of concealed Brugada syndrome in patients with atrioventricular nodal reentrant tachycardia

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Brugada Syndrome

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1 reference

https://pubmed.ncbi.nlm.nih.gov/27485484

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A mutation in CALM1 encoding calmodulin in familial idiopathic ventricular fibrillation in childhood and adolescence

1 reference

https://pubmed.ncbi.nlm.nih.gov/27485484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Conduction between isolated rabbit Purkinje and ventricular myocytes coupled by a variable resistance

1 reference

https://pubmed.ncbi.nlm.nih.gov/27485484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevention of Ventricular Fibrillation Episodes in Brugada Syndrome by Catheter Ablation Over the Anterior Right Ventricular Outflow Tract Epicardium

1 reference

https://pubmed.ncbi.nlm.nih.gov/27485484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fever increases the risk for cardiac arrest in the Brugada syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/27485484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.1038/SREP30967

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20 March 2020

PMC publication ID

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20 March 2020

PubMed publication ID

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20 March 2020

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