Article
Invertebrate models of lamin diseases.
Nucleus (Austin, Tex.) - 1 Jan 2018
Rzepecki Ryszard, Gruenbaum Yosef
Abstract excerpt
Lamins are evolutionarily conserved nuclear intermediate filament proteins. They provide structural support for the nucleus and help regulate many other nuclear activities. Mutations in human lamin genes, and especially in the LMNA gene, cause numerous diseases, termed laminopathies, including muscle, cardiac, metabolic, neuronal and early aging diseases. Most laminopathies arise from autosomal dominant missense...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
