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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:BMC Med
Hauptverfasser: Yatsenko, Andriy S., Kucherenko, Mariya M., Xie, Yuanbin, Aweida, Dina, Urlaub, Henning, Scheibe, Renate J., Cohen, Shenhav, Shcherbata, Halyna R.
Format: Artigo
Sprache:Inglês
Veröffentlicht: BioMed Central 2020
Schlagworte:
Research Article
Online Zugang: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
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!

Ähnliche Einträge