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Plasma lipidomic analysis shows a disease progression signature in mdx mice

Duchenne muscular dystrophy (DMD) is a rare genetic disorder affecting paediatric patients. The disease course is characterized by loss of muscle mass, which is rapidly substituted by fibrotic and adipose tissue. Clinical and preclinical models have clarified the processes leading to muscle damage a...

Ausführliche Beschreibung

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Bibliographische Detailangaben
Veröffentlicht in:Sci Rep
Hauptverfasser: Tsonaka, Roula, Seyer, Alexandre, Aartsma-Rus, Annemieke, Spitali, Pietro
Format: Artigo
Sprache:Inglês
Veröffentlicht: Nature Publishing Group UK 2021
Schlagworte:
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC8217252/
https://ncbi.nlm.nih.gov/pubmed/34155298
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-021-92406-6
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