Cargando…
Lamin A/C–mediated neuromuscular junction defects in Emery-Dreifuss muscular dystrophy
The LMNA gene encodes lamins A and C, two intermediate filament-type proteins that are important determinants of interphase nuclear architecture. Mutations in LMNA lead to a wide spectrum of human diseases including autosomal dominant Emery-Dreifuss muscular dystrophy (AD-EDMD), which affects skelet...
Autores principales: | Méjat, Alexandre, Decostre, Valérie, Li, Juan, Renou, Laure, Kesari, Akanchha, Hantaï, Daniel, Stewart, Colin L., Xiao, Xiao, Hoffman, Eric, Bonne, Gisèle, Misteli, Tom |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2615092/ https://www.ncbi.nlm.nih.gov/pubmed/19124654 http://dx.doi.org/10.1083/jcb.200811035 |
Ejemplares similares
-
Emery‐Dreifuss muscular dystrophy
por: Heller, Scott A., et al.
Publicado: (2019) -
Lamin A/C Assembly Defects in LMNA-Congenital Muscular Dystrophy Is Responsible for the Increased Severity of the Disease Compared with Emery–Dreifuss Muscular Dystrophy
por: Bertrand, Anne T., et al.
Publicado: (2020) -
Effect of genetic background on the cardiac phenotype in a mouse model of Emery-Dreifuss muscular dystrophy
por: Vignier, Nicolas, et al.
Publicado: (2019) -
Clinical aspects of Emery-Dreifuss muscular dystrophy
por: Madej-Pilarczyk, Agnieszka
Publicado: (2018) -
An Omics View of Emery–Dreifuss Muscular Dystrophy
por: Vignier, Nicolas, et al.
Publicado: (2020)