Article
Impaired mechanical response of an EDMD mutation leads to motility phenotypes that are repaired by loss of prenylation.
Journal of cell science - 1 May 2016
Zuela Noam, Zwerger Monika, Levin Tal, Medalia Ohad, Gruenbaum Yosef
Abstract excerpt
There are roughly 14 distinct heritable autosomal dominant diseases associated with mutations in lamins A/C, including Emery-Dreifuss muscular dystrophy (EDMD). The mechanical model proposes that the lamin mutations change the mechanical properties of muscle nuclei, leading to cell death and tissue deterioration. Here, we developed an experimental protocol that analyzes the effect of disease-linked lamin...
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