Profiling of the muscle-specific dystroglycan interactome reveals the role of Hippo signaling in muscular dystrophy and age-dependent muscle atrophy

BACKGROUND: Dystroglycanopathies are a group of inherited disorders characterized by vast clinical and genetic heterogeneity and caused by abnormal functioning of the ECM receptor dystroglycan (Dg). Remarkably, among many cases of diagnosed dystroglycanopathies, only a small fraction can be linked d...

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Detalles Bibliográficos
Autores principales: Yatsenko, Andriy S., Kucherenko, Mariya M., Xie, Yuanbin, Aweida, Dina, Urlaub, Henning, Scheibe, Renate J., Cohen, Shenhav, Shcherbata, Halyna R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971923/
https://www.ncbi.nlm.nih.gov/pubmed/31959160
http://dx.doi.org/10.1186/s12916-019-1478-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971923/
https://www.ncbi.nlm.nih.gov/pubmed/31959160
http://dx.doi.org/10.1186/s12916-019-1478-3

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