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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Detalhes bibliográficos
Publicado no:BMC Med
Main Authors: Yatsenko, Andriy S., Kucherenko, Mariya M., Xie, Yuanbin, Aweida, Dina, Urlaub, Henning, Scheibe, Renate J., Cohen, Shenhav, Shcherbata, Halyna R.
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2020
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6971923/
https://ncbi.nlm.nih.gov/pubmed/31959160
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12916-019-1478-3
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