Aberrant Protein Turn-Over Associated With Myofibrillar Disorganization in FHL1 Knockout Mice

Mutations in the FHL1 gene, and FHL1 protein deletion, are associated with rare hereditary myopathies and cardiomyopathies. FHL1-null mice develop age-dependent myopathy and increased autophagic activity. However, the molecular pathway involved in contractile function and increased autophagic activi...

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Detalles Bibliográficos
Autores principales: Ding, Jingjing, Cong, Yan Fei, Liu, Bo, Miao, Jianing, Wang, Lili
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065255/
https://www.ncbi.nlm.nih.gov/pubmed/30083183
http://dx.doi.org/10.3389/fgene.2018.00273

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065255/
https://www.ncbi.nlm.nih.gov/pubmed/30083183
http://dx.doi.org/10.3389/fgene.2018.00273

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