Subcellular diversity of Nav1.5 in cardiomyocytes: distinct functions, mechanisms and targets-Reference-Cited by-同舟云学术

Subcellular diversity of Nav1.5 in cardiomyocytes: distinct functions, mechanisms and targets

Published:2022-12-19 Issue:5 Volume:601 Page:941-960
ISSN:0022-3751
Container-title:The Journal of Physiology
language:en
Short-container-title:The Journal of Physiology

Author:

Marchal Gerard A.¹²^ORCID,Remme Carol Ann¹^ORCID

Affiliation:

1. Department of Experimental Cardiology Heart Centre, Amsterdam Cardiovascular Sciences, Heart Failure & Arrhythmias Amsterdam UMC location University of Amsterdam Amsterdam The Netherlands

2. National Institute of Optics National Research Council (CNR‐INO) Sesto Fiorentino FlorenceItaly

Funder

ZonMw

Fondation Leducq

Publisher

Wiley

Subject

Physiology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1113/JP283086

Reference125 articles.

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

2. Super-resolution imaging reveals that loss of the C-terminus of connexin43 limits microtubule plus-end capture and NaV1.5 localization at the intercalated disc

3. An Ankyrin-Based Mechanism for Functional Organization of Dystrophin and Dystroglycan

4. [Na+]i and the driving force of the Na+/Ca2+-exchanger in heart failure

5. The Cardiac Sodium Channel: Gating Function and Molecular Pharmacology

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