Fibrogenesis in LAMA2-Related Muscular Dystrophy Is a Central Tenet of Disease Etiology
Author:
Publisher
Frontiers Media SA
Subject
Cellular and Molecular Neuroscience,Molecular Biology
Reference93 articles.
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4. Restoration of muscle strength in dystrophic muscle by angiotensin-1-7 through inhibition of TGF-beta signalling.;Acuna;Hum. Mol. Genet.,2014
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1. A Multicenter Cross-Sectional Study of the Swiss Cohort of LAMA2-Related Muscular Dystrophy;Journal of Neuromuscular Diseases;2024-09-03
2. Pharmacological Treatments and Therapeutic Targets in Muscle Dystrophies Generated by Alterations in Dystrophin-Associated Proteins;Medicina;2024-06-27
3. Apelin stimulation of the vascular skeletal muscle stem cell niche enhances endogenous repair in dystrophic mice;Science Translational Medicine;2024-03-20
4. SNUPN deficiency causes a recessive muscular dystrophy due to RNA mis-splicing and ECM dysregulation;Nature Communications;2024-02-27
5. Deregulation of multiple mechanisms shapes the onset ofLAMA2-congenital muscular dystrophy;2024-01-24
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