ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene. - Wikidata - wikimedia - TriplyDB

ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene.

ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene.

http://www.wikidata.org/entity/Q37627289

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Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome Early Repolarization Syndrome; Mechanistic Theories and Clinical Correlates The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance Genetics of channelopathies associated with sudden cardiac death Genetics of inherited primary arrhythmia disorders Electrophysiological Mechanisms of Brugada Syndrome: Insights from Pre-clinical and Clinical Studies Genetics of Brugada syndrome ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology.The new kids on the block of arrhythmogenic disorders: Short QT Syndrome and early repolarization.Ranolazine for Congenital Long-QT Syndrome Type III: Experimental and Long-Term Clinical Data.A Brugada syndrome proband with compound heterozygote SCN5A mutations identified from a Chinese family in Singapore.The Diagnosis, Risk Stratification, and Treatment of Brugada Syndrome A novel mutation in the SCN5A gene contributes to arrhythmogenic characteristics of early repolarization syndrome.A mutation in the CACNA1C gene leads to early repolarization syndrome with incomplete penetrance: A Chinese family study.J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge Genetics of Brugada syndrome.Evaluation of the Genetic Basis of Familial Aggregation of Pacemaker Implantation by a Large Next Generation Sequencing Panel.ABCC9/SUR2 in the brain: Implications for hippocampal sclerosis of aging and a potential therapeutic target.KATP Channels in the Cardiovascular System.Brugada Syndrome: Clinical, Genetic, Molecular, Cellular, and Ionic Aspects.Cellular and ionic mechanisms underlying the effects of cilostazol, milrinone, and isoproterenol to suppress arrhythmogenesis in an experimental model of early repolarization syndrome.Novel Therapeutic Strategies for the Management of Ventricular Arrhythmias Associated with the Brugada Syndrome Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect.Brugada Syndrome and Early Repolarisation: Distinct Clinical Entities or Different Phenotypes of the Same Genetic Disease?Brugada syndrome: clinical and genetic findings.Evaluation Of Patients With Early Repolarization Syndrome Phosphorylation-dependent changes in nucleotide binding, conformation, and dynamics of the first nucleotide binding domain (NBD1) of the sulfonylurea receptor 2B (SUR2B).Cantú Syndrome Associated with Ovarian Agenesis.Sanger sequencing as a first-line approach for molecular diagnosis of Andersen-Tawil syndrome.The Cumulative Effects of the MYH7-V878A and CACNA1C-A1594V Mutations in a Chinese Family with Hypertrophic Cardiomyopathy.Prognosis, risk stratification, and management of asymptomatic individuals with Brugada syndrome: A systematic review.Novel mutation in ABBC9 gene associated with congenital hypertrichosis and acromegaloid facial features, without cardiac or skeletal anomalies: a new phenotype.Ion Channel Disorders and Sudden Cardiac Death.J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge.Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome High risk electrocardiographic markers in Brugada syndrome.Calcium in Brugada Syndrome: Questions for Future Research Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations High-throughput genetic characterization of a cohort of Brugada syndrome patients

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ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene.

http://www.wikidata.org/entity/Q37627289

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

@pt

bilimsel makale

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scientific article published on 04 January 2014

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene.

@en

ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene.

@nl

type

label

ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene.

@en

ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene.

@nl

prefLabel

ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene.

@en

ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene.

@nl

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J.IJCARD.2013.12.084

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International Journal of Cardiology

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ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene

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Andre Terzic

http://www.w3.org/2001/XMLSchema#string

Christian Veltmann

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Daniela Ponce-Balbuena

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Elena Burashnikov

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Gi-Byong Nam

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Hector Barajas-Martínez

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John J Cai

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Jonathan Steinberg

http://www.w3.org/2001/XMLSchema#string

José Antonio Sánchez-Chapula

http://www.w3.org/2001/XMLSchema#string

Mark Preminger

http://www.w3.org/2001/XMLSchema#string

P2860

Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches

ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating

Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors

Gain-of-function mutation S422L in the KCNJ8-encoded cardiac K(ATP) channel Kir6.1 as a pathogenic substrate for J-wave syndromes

Principles governing amino acid composition of integral membrane proteins: application to topology prediction

Ventricular fibrillation in a patient with prominent J (Osborn) waves and ST segment elevation in the inferior electrocardiographic leads: a Brugada syndrome variant?

Electrophysiological characterization of SCN5A mutations causing long QT (E1784K) and Brugada (R1512W and R1432G) syndromes.

Natural history of Brugada syndrome: insights for risk stratification and management.

Sudden cardiac arrest associated with early repolarization.

Identification of six novel SCN5A mutations in Japanese patients with Brugada syndrome.

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431-442

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scholarly article

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10.1016/J.IJCARD.2013.12.084

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3

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171

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Charles Antzelevitch

Angelica López-Izquierdo

Martin Borggrefe

Christian Wolpert

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2014-01-04T00:00:00Z

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259806278

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24439875

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potassium channel activity

ATP binding cassette subfamily C member 9

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3947869

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