Depletion of extracellular signal-regulated kinase 1 in mice with cardiomyopathy caused by lamin A/C gene mutation partially prevents pathology before isoenzyme activation
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/23/1/1/2136955/ddt387.pdf
Reference43 articles.
1. The Nuclear Envelope as a Signaling Node in Development and Disease
2. Laminopathies and the long strange trip from basic cell biology to therapy
3. LMNA cardiomyopathy: cell biology and genetics meet clinical medicine
4. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy
5. Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System Disease
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