Transcriptional profiling in facioscapulohumeral muscular dystrophy to identify candidate biomarkers
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference47 articles.
1. Facioscapulohumeral muscular dystrophy
2. On the significance of retinal vascular disease and hearing loss in facioscapulohumeral muscular dystrophy
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1. Muscle strength, quantity and quality and muscle fat quantity and their association with oxidative stress in patients with facioscapulohumeral muscular dystrophy: Effect of antioxidant supplementation;Free Radical Biology and Medicine;2024-07
2. Meta-analysis towards FSHD reveals misregulation of neuromuscular junction, nuclear envelope, and spliceosome;Communications Biology;2024-05-25
3. Single-cell spatial transcriptomics reveals a dystrophic trajectory following a developmental bifurcation of myoblast cell fates in facioscapulohumeral muscular dystrophy;Genome Research;2024-05
4. Engineered FSHD mutations results in D4Z4 heterochromatin disruption and feedforward DUX4 network activation;iScience;2024-04
5. An up-to-date myopathologic characterisation of facioscapulohumeral muscular dystrophy type 1 muscle biopsies shows sarcolemmal complement membrane attack complex deposits and increased skeletal muscle regeneration;Neuromuscular Disorders;2024-03
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