Mutation-independent proteomic signatures of pathological progression in murine models of Duchenne muscular dystrophy.

This study provides novel insights into mutation-independent proteomic signatures characteristic of the dystrophic phenotype and its progression with aging.
PMID: 32994316 [PubMed - as supplied by publisher]

Source: Molecular and Cellular Proteomics : MCP - September 28, 2020 Category: Molecular Biology Authors: van Westering TLE, Johansson HJ, Hanson B, Coenen-Stass AML, Lomonosova Y, Tanihata J, Motohashi N, Yokota T, Takeda S, Lehtiö J, Wood MJA, El Andaloussi S, Aoki Y, Roberts TC Tags: Mol Cell Proteomics Source Type: research