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Article

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

BMC medicine - 21 Jan 2020

Yatsenko Andriy S, Kucherenko Mariya M, Xie Yuanbin, Aweida Dina, Urlaub Henning, Scheibe Renate J, Cohen Shenhav, Shcherbata Halyna R

Abstract excerpt

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 directly to mutations in Dg or its regulatory enzymes, implying the involvement of other, not-yet-characterized,...

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Identifiers

PMID: 31959160
DOI: 10.1186/s12916-019-1478-3
PMCID: PMC6971923

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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