Highly efficient in vivo delivery of PMO into regenerating myotubes and rescue in laminin-α2 chain-null congenital muscular dystrophy mice. [electronic resource]
Producer: 20140722Description: 4914-28 p. digitalISSN:- 1460-2083
- Alternative Splicing
- Animals
- Base Sequence
- Bromodeoxyuridine -- metabolism
- Cardiotoxins -- administration & dosage
- Cell Line
- Cell Membrane Permeability -- genetics
- Disease Models, Animal
- Dystrophin -- chemistry
- Exons
- Gene Expression
- Gene Order
- Humans
- Laminin -- genetics
- Mice
- Mice, Knockout
- Morpholinos -- administration & dosage
- Muscle Fibers, Skeletal -- classification
- Muscular Dystrophies -- genetics
- Muscular Dystrophy, Animal
- Muscular Dystrophy, Duchenne -- genetics
- Regeneration
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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