(Q24294117)

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Defining the cellular phenotype of "ankyrin-B syndrome" variants: human ANK2 variants associated with clinical phenotypes display a spectrum of activities in cardiomyocytes

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Defining the cellular phenotype of "ankyrin-B syndrome" variants: human ANK2 variants associated with clinical phenotypes display a spectrum of activities in cardiomyocytes (English)

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GOA release 2020-03-11

regulation of heart rate by cardiac conduction

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GOA release 2020-03-11

Ankyrin 2, brain

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GOA release 2020-03-11

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Jean-Jacques Schott

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12

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Solena Le Scouarnec

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Pascale Guicheney

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13

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Dan M Roden

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Peter J Mohler

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author name string

Isabelle Denjoy

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John S Lowe

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Lise Caron

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Iwona M Driskell

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Kris Norris

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Antoine Leenhardt

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Richard B Kim

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publication date

30 January 2007

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115

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432-41

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4

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Brugada syndrome: report of the second consensus conference.

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https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.656512

7 January 2021

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Targeted mutational analysis of ankyrin-B in 541 consecutive, unrelated patients referred for long QT syndrome genetic testing and 200 healthy subjects

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https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.656512

7 January 2021

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Human genomics and its impact on arrhythmias

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https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.656512

7 January 2021

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Molecular biology and the prolonged QT syndromes

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https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.656512

7 January 2021

based on heuristic

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Molecular and cellular mechanisms of cardiac arrhythmias

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https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.656512

7 January 2021

based on heuristic

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Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

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https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.656512

7 January 2021

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A cardiac arrhythmia syndrome caused by loss of ankyrin-B function

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https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.656512

7 January 2021

based on heuristic

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The ankyrin-B C-terminal domain determines activity of ankyrin-B/G chimeras in rescue of abnormal inositol 1,4,5-trisphosphate and ryanodine receptor distribution in ankyrin-B (-/-) neonatal cardiomyocytes

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https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.656512

7 January 2021

based on heuristic

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Inositol 1,4,5-trisphosphate receptor localization and stability in neonatal cardiomyocytes requires interaction with ankyrin-B

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https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.656512

7 January 2021

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Isoform specificity among ankyrins. An amphipathic alpha-helix in the divergent regulatory domain of ankyrin-b interacts with the molecular co-chaperone Hdj1/Hsp40.

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.656512

7 January 2021

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Ankyrin-B targets beta2-spectrin to an intracellular compartment in neonatal cardiomyocytes

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https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.656512

7 January 2021

based on heuristic

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Isoform specificity of ankyrin-B: a site in the divergent C-terminal domain is required for intramolecular association

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https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.656512

7 January 2021

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Molecular physiology of cardiac repolarization

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https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.656512

7 January 2021

based on heuristic

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Spectrin and ankyrin-based pathways: metazoan inventions for integrating cells into tissues

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https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.656512

7 January 2021

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Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes

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https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.656512

7 January 2021

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Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.656512

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetics of acquired long QT syndrome

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.656512

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetics of cardiac arrhythmias and sudden cardiac death

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.656512

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1161/CIRCULATIONAHA.106.656512

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