Mutant lamins cause nuclear envelope rupture and DNA damage in skeletal muscle cells

Mutations in the LMNA gene, which encodes the nuclear envelope (NE) proteins lamins A/C, cause Emery-Dreifuss muscular dystrophy, congenital muscular dystrophy, and other diseases collectively known as laminopathies. The mechanisms responsible for these diseases remain incompletely understood. Using...

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Detalles Bibliográficos
Autores principales: Earle, Ashley J., Kirby, Tyler J., Fedorchak, Gregory R., Isermann, Philipp, Patel, Jineet, Iruvanti, Sushruta, Moore, Steven A., Bonne, Gisèle, Wallrath, Lori L., Lammerding, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7102937/
https://www.ncbi.nlm.nih.gov/pubmed/31844279
http://dx.doi.org/10.1038/s41563-019-0563-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7102937/
https://www.ncbi.nlm.nih.gov/pubmed/31844279
http://dx.doi.org/10.1038/s41563-019-0563-5

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