Apoptosis inhibitors and mini-agrin have additive benefits in congenital muscular dystrophy mice

Mutations in LAMA2 cause a severe form of congenital muscular dystrophy, called MDC1A. Studies in mouse models have shown that transgenic expression of a designed, miniaturized form of the extracellular matrix molecule agrin (‘mini-agrin’) or apoptosis inhibition by either overexpression of Bcl2 or...

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Detalles Bibliográficos
Autores principales: Meinen, Sarina, Lin, Shuo, Thurnherr, Raphael, Erb, Michael, Meier, Thomas, Rüegg, Markus A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: WILEY-VCH Verlag 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3377088/
https://www.ncbi.nlm.nih.gov/pubmed/21674808
http://dx.doi.org/10.1002/emmm.201100151

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3377088/
https://www.ncbi.nlm.nih.gov/pubmed/21674808
http://dx.doi.org/10.1002/emmm.201100151

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