Deep dive into muscle repair yields new strategies to combat Duchenne muscular dystrophy
By A Mystery Man Writer
Description
Researchers at the Sanford Burnham Prebys Medical Discovery Institute (SBP) reported new findings this week that may lead to novel therapeutic strategies for people suffering from Duchenne muscular dystrophy (DMD). DMD, a muscle-wasting disease that affects 1 in 7250 males aged 5 to 24 years in the United States, is caused by a genetic mutation leading…
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Muscle and cardiac therapeutic strategies for Duchenne muscular dystrophy: past, present, and future
Piezo1 Possible Key to Supporting Muscle Regeneration in Duchenne Muscular Dystrophy - Penn Medicine
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Frontiers Combined Therapies for Duchenne Muscular Dystrophy to
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Regenerative Rehabilitation for Duchenne Muscular Dystrophy
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Proteomes, Free Full-Text
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Muscular Dystrophy
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Todd Dubnicoff The Stem Cellar
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Genes, Free Full-Text
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PDF) Delivery challenges for CRISPR—Cas9 genome editing for Duchenne muscular dystrophy
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New treatment could benefit up to 45 per cent of patients with
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Duchenne muscular dystrophy, The Stem Cellar
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