Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth

Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth

Laminopathies are a clinically heterogeneous group of disorders caused by mutations in the <i>LMNA</i> gene, which encodes the nuclear envelope proteins lamins A and C. The most frequent diseases associated with <i>LMNA</i> mutations are characterized by skeletal and cardiac...

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Bibliographic Details
Main Authors: Daniel J. Owens, Julien Messéant, Sophie Moog, Mark Viggars, Arnaud Ferry, Kamel Mamchaoui, Emmanuelle Lacène, Norma Roméro, Astrid Brull, Gisèle Bonne, Gillian Butler-Browne, Catherine Coirault
Format: Article
Language:English
Published: MDPI AG 2021-12-01
Series:International Journal of Molecular Sciences
Subjects:
mechanotransduction
muscle growth
nuclear envelope
satellite cell
YAP
Online Access:https://www.mdpi.com/1422-0067/22/1/306

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https://www.mdpi.com/1422-0067/22/1/306

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