Discovery of potential urine-accessible metabolite biomarkers associated with muscle disease and corticosteroid response in the mdx mouse model for Duchenne
Author:
Funder
National Cancer Institute
Muscular Dystrophy Association
American Academy of Neurology/American Brain Foundation
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
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4. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals;M Koenig;Cell,1987
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1. Biomarkers in Duchenne Muscular Dystrophy;Current Heart Failure Reports;2022-04
2. Tetrahydrobiopterin synthesis and metabolism is impaired in dystrophin‐deficient mdx mice and humans;Acta Physiologica;2021-03-08
3. Biomarkers for Duchenne muscular dystrophy: myonecrosis, inflammation and oxidative stress;Disease Models & Mechanisms;2020-02-01
4. Longitudinal metabolomic analysis of plasma enables modeling disease progression in Duchenne muscular dystrophy mouse models;Human Molecular Genetics;2020-01-10
5. Identification of marker proteins of muscular dystrophy in the urine proteome from the mdx-4cv model of dystrophinopathy;Molecular Omics;2020
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