Uncoordinated transcription and compromised muscle function in the lmna-null mouse model of Emery- Emery-Dreyfuss muscular dystrophy.
LMNA encodes both lamin A and C: major components of the nuclear lamina. Mutations in LMNA underlie a range of tissue-specific degenerative diseases, including those that affect skeletal muscle, such as autosomal-Emery-Dreifuss muscular dystrophy (A-EDMD) and limb girdle muscular dystrophy 1B. Here,...
Main Authors: | Viola F Gnocchi, Juergen Scharner, Zhe Huang, Ken Brady, Jaclyn S Lee, Robert B White, Jennifer E Morgan, Yin-Biao Sun, Juliet A Ellis, Peter S Zammit |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2011-02-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC3043058?pdf=render |
Similar Items
-
Novel LMNA Mutation in a Taiwanese Family with Autosomal Dominant Emery-Dreifuss Muscular Dystrophy
by: Wen-Chen Liang, et al.
Published: (2007-01-01) -
LMNA mutation leads to cardiac sodium channel dysfunction in the Emery-Dreifuss muscular dystrophy patient
by: Kseniya Perepelina, et al.
Published: (2022-07-01) -
An Omics View of Emery–Dreifuss Muscular Dystrophy
by: Nicolas Vignier, et al.
Published: (2020-06-01) -
Distrofia muscular de Emery-Dreifuss: relato de caso Emery-Dreifuss muscular dystrophy: case report
by: Ana Lucila Moreira Carsten, et al.
Published: (2006-06-01) -
Samp1 Mislocalization in Emery-Dreifuss Muscular Dystrophy
by: Elisabetta Mattioli, et al.
Published: (2018-10-01)