(Q33618629)

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Flecainide inhibits arrhythmogenic Ca2+ waves by open state block of ryanodine receptor Ca2+ release channels and reduction of Ca2+ spark mass.

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scholarly article

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10 February 2020

Flecainide inhibits arrhythmogenic Ca2+ waves by open state block of ryanodine receptor Ca2+ release channels and reduction of Ca2+ spark mass (English)

1 reference

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10 February 2020

Bjorn C. Knollmann

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10 February 2020

author name string

Fredrick A Hilliard

1

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10 February 2020

Derek S Steele

2

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10 February 2020

Derek Laver

3

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10 February 2020

Zhaokang Yang

4

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10 February 2020

Sylvain J Le Marchand

5

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10 February 2020

Nagesh Chopra

6

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10 February 2020

David W Piston

7

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10 February 2020

Sabine Huke

8

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10 February 2020

publication date

14 October 2009

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10 February 2020

Journal of Molecular and Cellular Cardiology

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10 February 2020

48

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10 February 2020

293-301

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10 February 2020

2

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10 February 2020

describes a project that uses

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11 June 2022

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1 reference

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Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans

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The sarcoplasmic reticulum and arrhythmogenic calcium release

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The ryanodine receptor pore blocker neomycin also inhibits channel activity via a previously undescribed high-affinity Ca(2+) binding site

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SparkMaster: automated calcium spark analysis with ImageJ

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Casq2 deletion causes sarcoplasmic reticulum volume increase, premature Ca2+ release, and catecholaminergic polymorphic ventricular tachycardia

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10.1016/J.YJMCC.2009.10.005

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Europe PubMed Central

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10 February 2020

1 reference

Europe PubMed Central

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10 February 2020

1 reference

Europe PubMed Central

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10 February 2020

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