ERK1/2 directly acts on CTGF/CCN2 expression to mediate myocardial fibrosis in cardiomyopathy caused by mutations in the lamin A/C gene-Reference-Cited by-同舟云学术

ERK1/2 directly acts on CTGF/CCN2 expression to mediate myocardial fibrosis in cardiomyopathy caused by mutations in the lamin A/C gene

Published:2016-04-30 Issue:11 Volume:25 Page:2220-2233
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum. Mol. Genet.

Author:

Chatzifrangkeskou Maria,Le Dour Caroline,Wu Wei,Morrow John P.,Joseph Leroy C.,Beuvin Maud,Sera Fusako,Homma Shunichi,Vignier Nicolas,Mougenot Nathalie,Bonne Gisèle,Lipson Kenneth E.,Worman Howard J.,Muchir Antoine

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/25/11/2220/18526698/ddw090.pdf

Reference65 articles.

1. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

2. Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System Disease

3. Primary Prevention of Sudden Death in Patients with Lamin A/C Gene Mutations

4. Heart involvement in lamin A/C related diseases;Ben Yaou;Arch. Mal. Coeur Vaiss,2006

5. CMR-Verified Interstitial Myocardial Fibrosis as a Marker of Subclinical Cardiac Involvement in LMNA Mutation Carriers

Cited by 80 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. Myocardial fibrosis from the perspective of the extracellular matrix: Mechanisms to clinical impact;Matrix Biology;2024-12

3. Risk Assessment and Personalized Treatment Options in Inherited Dilated Cardiomyopathies: A Narrative Review;Biomedicines;2024-07-24

5. mTOR Inhibition Prolongs Survival and Has Beneficial Effects on Heart Function After Onset of Lamin A/C Gene Mutation Cardiomyopathy in Mice;Circulation: Heart Failure;2024-04