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ProteomicsiTRAQ Protemics of mdx vs. mdx/Actg1-TG mouse skeletal muscle
Duchenne muscular dystrophy (DMD) is an X-linked recessive disease caused by deleterious mutations in the DMD gene, rendering non-functional forms or complete absence of the protein dystrophin. Eccentric contraction-induced force loss is the most robust and reproducible phenotype of dystrophin-defic...
ORGANISM(S): Mus musculus (Mouse) 
2018-10-22 | PXD009680 | Pride
Mdx Itraq Skeletal muscle 
ProteomicsSplit intein mdx skeletal muscle proteomics
Duchenne muscular dystrophy is a rare and lethal neuromuscular disease caused by loss-of-function mutations in the dystrophin protein that provides structural integrity to striated muscle fibers. Mice with loss-of-function mutations for the Dmd gene encoding dystrophin (mdx-4cv) were treated with mi...
ORGANISM(S): Mus musculus (Mouse) 
2025-11-06 | PXD062324 | Pride
Aav therapy Split-intein Duchenne muscular dystrophy Skeletal muscle Lcms 
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