Rescuing cardiac automaticity in L-type Cav1.3 channelopathies and beyond

Author:

Mesirca Pietro123,Bidaud Isabelle123,Mangoni Matteo E.123

Affiliation:

1. Département de Physiologie; Institut de Genomique Fonctionnelle, LabEx ICST, UMR-5203, Centre national de la recherche scientifique; F-34094 Montpellier France

2. INSERM U1191; F-34094 Montpellier France

3. Université de Montpellier; F-34094 Montpellier France

Funder

Agence Nationale de la Recherche

European Union Research Programme

Publisher

Wiley

Subject

Physiology

Reference62 articles.

1. Control of heart rate by cAMP sensitivity of HCN channels;Alig;Proc Natl Acad Sci USA,2009

2. Loss of Cav1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness;Baig;Nat Neurosci,2011

3. A gain-of-function mutation in the cardiac pacemaker HCN4 channel increasing cAMP sensitivity is associated with familial Inappropriate Sinus Tachycardia;Baruscotti;Eur Heart J,2016

4. Deep bradycardia and heart block caused by inducible cardiac-specific knockout of the pacemaker channel gene Hcn4;Baruscotti;Proc Natl Acad Sci USA,2011

5. Sinoatrial nodal cell ryanodine receptor and Na+-Ca2+ exchanger: molecular partners in pacemaker regulation;Bogdanov;Circ Res,2001

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