Unmasking the molecular link between arrhythmogenic cardiomyopathy and Brugada syndrome.

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Sudden Unexplained Nocturnal Death Syndrome: The Hundred Years' Enigma.Coding variants in and increase risk of atrial fibrillation

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Unmasking the molecular link between arrhythmogenic cardiomyopathy and Brugada syndrome.

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http://www.wikidata.org/entity/Q39432304

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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Unmasking the molecular link between arrhythmogenic cardiomyopathy and Brugada syndrome.

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Unmasking the molecular link between arrhythmogenic cardiomyopathy and Brugada syndrome.

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Item

label

Unmasking the molecular link between arrhythmogenic cardiomyopathy and Brugada syndrome.

@en

Unmasking the molecular link between arrhythmogenic cardiomyopathy and Brugada syndrome.

@nl

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Unmasking the molecular link between arrhythmogenic cardiomyopathy and Brugada syndrome.

@en

Unmasking the molecular link between arrhythmogenic cardiomyopathy and Brugada syndrome.

@nl

P1476

Unmasking the molecular link between arrhythmogenic cardiomyopathy and Brugada syndrome.

@en

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Ramon Brugada

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Arrhythmogenic right ventricular cardiomyopathy/dysplasia

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias

Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome

Mutations in the area composita protein αT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy

Disease mutations in desmoplakin inhibit Cx43 membrane targeting mediated by desmoplakin-EB1 interactions.

Voltage-gated Nav channel targeting in the heart requires an ankyrin-G dependent cellular pathway

Plakophilin 2: a critical scaffold for PKC alpha that regulates intercellular junction assembly

Nav1.5 E1053K mutation causing Brugada syndrome blocks binding to ankyrin-G and expression of Nav1.5 on the surface of cardiomyocytes

A novel desmocollin-2 mutation reveals insights into the molecular link between desmosomes and gap junctions

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744-756

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scholarly article

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10.1038/NRCARDIO.2017.103

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English

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

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Javier Moncayo-Arlandi

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2017-07-13T00:00:00Z

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28703223

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Unmasking the molecular link between arrhythmogenic cardiomyopathy and Brugada syndrome.

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P2860

P2860

Unmasking the molecular link between arrhythmogenic cardiomyopathy and Brugada syndrome.

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P1433

P1476

P2093

P2860

P304

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P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698