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Lentiviral vectors can be used for full-length dystrophin gene therapy.
Counsell JR, Asgarian Z, Meng J, Ferrer V, Vink CA, Howe SJ, Waddington SN, Thrasher AJ, Muntoni F, Morgan JE, Danos O. Counsell JR, et al. Among authors: morgan je. Sci Rep. 2017 Mar 6;7(1):79. doi: 10.1038/s41598-017-00152-5. Sci Rep. 2017. PMID: 28250438 Free PMC article.
Lentiviral vectors can be used for full-length dystrophin gene therapy.
Counsell JR, Asgarian Z, Meng J, Ferrer V, Vink CA, Howe SJ, Waddington SN, Thrasher AJ, Muntoni F, Morgan JE, Danos O. Counsell JR, et al. Among authors: morgan je. Sci Rep. 2017 Mar 17;7:44775. doi: 10.1038/srep44775. Sci Rep. 2017. PMID: 28303972 Free PMC article.
Delivery of large transgene cassettes by foamy virus vector.
Sweeney NP, Meng J, Patterson H, Morgan JE, McClure M. Sweeney NP, et al. Among authors: morgan je. Sci Rep. 2017 Aug 14;7(1):8085. doi: 10.1038/s41598-017-08312-3. Sci Rep. 2017. PMID: 28808269 Free PMC article.
Stem cells to treat muscular dystrophies - where are we?
Meng J, Muntoni F, Morgan JE. Meng J, et al. Among authors: morgan je. Neuromuscul Disord. 2011 Jan;21(1):4-12. doi: 10.1016/j.nmd.2010.10.004. Epub 2010 Nov 4. Neuromuscul Disord. 2011. PMID: 21055938 Review.
518 results