Expression of Lmna-R225X nonsense mutation results in dilated cardiomyopathy and conduction disorders (DCM-CD) in mice: Impact of exercise training-Reference-Cited by-同舟云学术

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Expression of Lmna-R225X nonsense mutation results in dilated cardiomyopathy and conduction disorders (DCM-CD) in mice: Impact of exercise training

Published:2020-01 Issue: Volume:298 Page:85-92
ISSN:0167-5273
Container-title:International Journal of Cardiology
language:en
Short-container-title:International Journal of Cardiology

Author:

Cai Zhu-Jun,Lee Yee-Ki,Lau Yee-Man,Ho Jenny Chung-Yee,Lai Wing-Hon,Wong Navy Lai-Yung,Huang Duo,Hai Jo-jo,Ng Kwong-Man,Tse Hung-Fat,Siu Chung-Wah

Funder

Hong Kong Research Grant Council

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference27 articles.

1. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease;Fatkin;N. Engl. J. Med.,1999

2. Natural history of dilated cardiomyopathy due to lamin A/C gene mutations;Taylor;J. Am. Coll. Cardiol.,2003

3. Long-term outcome and risk stratification in dilated cardiolaminopathies;Pasotti;J. Am. Coll. Cardiol.,2008

4. A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation;Hershberger;Am. Heart J.,2002

5. Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death?;van Berlo;J. Mol. Med.,2005

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1. The Pathogenic Mechanisms of and Novel Therapies for Lamin A/C-Related Dilated Cardiomyopathy Based on Patient-Specific Pluripotent Stem Cell Platforms and Animal Models;Pharmaceuticals;2024-08-05

2. Non-cell-Autonomous Cardiomyocyte Regulation Complicates Gene Supplementation Therapy for Lmna-Associated Cardiac Defects in Mice;JACC: Basic to Translational Science;2024-08

3. In Vivo Approaches to Understand Arrhythmogenic Cardiomyopathy: Perspectives on Animal Models;Cells;2024-07-27

4. The structure and function of lamin A/C: Special focus on cardiomyopathy and therapeutic interventions;Life Sciences;2024-03

5. An alpha-helix variant p.Arg156Pro in LMNA as a cause of hereditary dilated cardiomyopathy: genetics and bioinfomatics exploration;BMC Medical Genomics;2023-10-02

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