Highly efficient in vivo delivery of PMO into regenerating myotubes and rescue in laminin-α2 chain-null congenital muscular dystrophy mice.
Document Type
Journal Article
Publication Date
12-15-2013
Journal
Human Molecular Genetics
Volume
22
Issue
24
Inclusive Pages
4914–4928
DOI
10.1093/hmg/ddt341
Keywords
Alternative Splicing; Animals; Base Sequence; Bromodeoxyuridine; Cardiotoxins; Cell Line; Cell Membrane Permeability; Disease Models, Animal; Dystrophin; Exons; Gene Expression; Gene Order; Humans; Laminin; Mice; Mice, Knockout; Morpholinos; Muscle Fibers, Skeletal; Muscular Dystrophies; Muscular Dystrophy, Animal; Muscular Dystrophy, Duchenne; Regeneration
APA Citation
Aoki, Y., Nagata, T., Yokota, T., Nakamura, A., Wood, M. J., Partridge, T., & Takeda, S. (2013). Highly efficient in vivo delivery of PMO into regenerating myotubes and rescue in laminin-α2 chain-null congenital muscular dystrophy mice.. Human Molecular Genetics, 22 (24). http://dx.doi.org/10.1093/hmg/ddt341
Peer Reviewed
1
- Citations
- Citation Indexes: 59
- Usage
- Abstract Views: 10
- Captures
- Readers: 82
- Mentions
- References: 2
