Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction

Mutations in the lamin A/C gene (LMNA) cause a variety of human diseases including Emery-Dreifuss muscular dystrophy, dilated cardiomyopathy, and Hutchinson-Gilford progeria syndrome. The tissue-specific effects of lamin mutations are unclear, in part because the function of lamin A/C is incompletel...

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Autors principals: Lammerding, Jan, Schulze, P. Christian, Takahashi, Tomosaburo, Kozlov, Serguei, Sullivan, Teresa, Kamm, Roger D., Stewart, Colin L., Lee, Richard T.
Format: Artigo
Idioma:Inglês
Publicat: American Society for Clinical Investigation 2004
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC324542/
https://ncbi.nlm.nih.gov/pubmed/14755334
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI200419670
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