Linker of nucleoskeleton and cytoskeleton complex proteins in cardiomyopathy
Author:
Funder
British Heart Foundation
Publisher
Springer Science and Business Media LLC
Subject
Molecular Biology,Structural Biology,Biophysics
Link
http://link.springer.com/article/10.1007/s12551-018-0431-6/fulltext.html
Reference229 articles.
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3. Arimura T et al (2005) Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies. Hum Mol Genet 14:155–169. https://doi.org/10.1093/hmg/ddi017
4. Astejada MN et al (2007) Emerinopathy and laminopathy clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in Japan. Acta Myol 26:159–164
5. Banerjee I et al (2014) Targeted ablation of nesprin 1 and nesprin 2 from murine myocardium results in cardiomyopathy, altered nuclear morphology and inhibition of the biomechanical gene response. PLoS Genet 10:e1004114. https://doi.org/10.1371/journal.pgen.1004114
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