Bioinformatic analysis of a plakophilin-2-dependent transcription network: implications for the mechanisms of arrhythmogenic right ventricular cardiomyopathy in humans and in boxer dogs

Author:

Montnach Jerome1,Agullo-Pascual Esperanza1,Tadros Rafik2,Bezzina Connie R2,Delmar Mario1

Affiliation:

1. The Leon H Charney Division of Cardiology, New York University School of Medicine, 435 East 30th Street. SB 707, New York, NY, USA

2. Department of Clinical and Experimental Cardiology, Heart Center, Academic Medical Center, Amsterdam, the Netherlands

Funder

Fondation Leducq Transatlantic Network of Excellence

CVON-PREDICT

Dutch Heart Foundation

Netherlands Organization for Scientific Research

Philippa and Marvin Carsley Chair in Cardiology

American Heart Association

Heart Rhythm Society

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference27 articles.

1. The cardiac desmosome and arrhythmogenic cardiomyopathies: from gene to disease;Delmar;Circ Res,2010

2. Clinical presentation, long-term follow-up, and outcomes of 1001 arrhythmogenic right ventricular dysplasia/cardiomyopathy patients and family members;Groeneweg;Circ Cardiovasc Genet,2015

3. Pathophysiology of arrhythmogenic cardiomyopathy;Basso;Nat Rev Cardiol,2012

4. Arrhythmogenic right ventricular cardiomyopathy;Basso;Lancet,2009

5. Comparison of features of fatal versus nonfatal cardiac arrest in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy;Gupta;Am J Cardiol,2017

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