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A dystrophic Duchenne mouse model for testing human antisense oligonucleotides | PLOS ONE
Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice | Nature Medicine
Treating Muscular Dystrophy with CRISPR Gene Editing
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PDF] The Crystal Structure of the Exon Junction Complex Reveals How It Maintains a Stable Grip on mRNA | Semantic Scholar
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Biomolecules | Free Full-Text | A Day in the Life of the Exon Junction Complex
PDF] The Crystal Structure of the Exon Junction Complex Reveals How It Maintains a Stable Grip on mRNA | Semantic Scholar
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Efficient Modulation of Exon Skipping via Antisense Circular RNAs | Research
JPM | Free Full-Text | Applications of CRISPR/Cas9 for the Treatment of Duchenne Muscular Dystrophy
Genes | Free Full-Text | Alternative Splicing Role in New Therapies of Spinal Muscular Atrophy
PDF] The Crystal Structure of the Exon Junction Complex Reveals How It Maintains a Stable Grip on mRNA | Semantic Scholar
The Crystal Structure of the Exon Junction Complex Reveals How It Maintains a Stable Grip on mRNA: Cell
The exon-junction complex helicase eIF4A3 controls cell fate via coordinated regulation of ribosome biogenesis and translational output | Science Advances
Development of DG9 peptide-conjugated single- and multi-exon skipping therapies for the treatment of Duchenne muscular dystrophy | PNAS
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Development of DG9 peptide-conjugated single- and multi-exon skipping therapies for the treatment of Duchenne muscular dystrophy