SAP97 and Dystrophin Macromolecular Complexes Determine Two Pools of Cardiac Sodium Channels Na v 1.5 in Cardiomyocytes-Reference-Cited by-同舟云学术

SAP97 and Dystrophin Macromolecular Complexes Determine Two Pools of Cardiac Sodium Channels Na v 1.5 in Cardiomyocytes

Published:2011-02-04 Issue:3 Volume:108 Page:294-304
ISSN:0009-7330
Container-title:Circulation Research
language:en
Short-container-title:Circ Res

Author:

Petitprez Séverine¹,Zmoos Anne-Flore¹,Ogrodnik Jakob¹,Balse Elise¹,Raad Nour¹,El-Haou Said¹,Albesa Maxime¹,Bittihn Philip¹,Luther Stefan¹,Lehnart Stephan E.¹,Hatem Stéphane N.¹,Coulombe Alain¹,Abriel Hugues¹

Affiliation:

1. From the Department of Clinical Research (S.P., A.-F.Z., J.O., M.A., H.A.), University of Bern, Switzerland; INSERM UMRS 956 (S.P., E.B., S.E.-H., S.N.H., A.C.), Université Pierre et Marie Curie-Paris 6, Paris, France; Max Planck Institute for Dynamics and Self-Organization (N.R., P.B., S.L.), Göttingen, Germany; Department of Cardiology & Pulmonology (N.R., S.E.L.), Heart Research Center Goettingen, University Medical Center Göttingen, Germany; Department of Biomedical Sciences (S.L.), Cornell...

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology

Reference35 articles.

1. SCN5A channelopathies – An update on mutations and mechanisms

2. Cardiac sodium channel Nav1.5 and interacting proteins: Physiology and pathophysiology

3. Molecular determinants of voltage-gated sodium channel regulation by the Nedd4/Nedd4-like proteins

4. Cardiac Sodium Channel Na v 1.5 Is Regulated by a Multiprotein Complex Composed of Syntrophins and Dystrophin

5. Function and Genetics of Dystrophin and Dystrophin-Related Proteins in Muscle

Cited by 224 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Nernst-Planck-Gaussian modelling of electrodiffusional recovery from ephaptic excitation between mammalian cardiomyocytes;Frontiers in Physiology;2024-01-03

2. The Kir2.1-NaV1.5 Channelosome and its role in Arrhythmias in Inheritable Cardiac Diseases;Heart Rhythm;2024-01

3. Unraveling Impacts of Chamber-Specific Differences in Intercalated Disc Ultrastructure and Molecular Organization on Cardiac Conduction;JACC: Clinical Electrophysiology;2023-12

4. Gene Therapy for Cardiomyopathy associated with Duchenne Muscular Dystrophy in a Pig Model;2023-10-03

5. Maturation of iPSC-derived cardiomyocytes in a heart-on-a-chip device enables modeling of dilated cardiomyopathy caused by R222Q-SCN5A mutation;Biomaterials;2023-10