Meng J - Search Results

1

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: meng j. Sci Rep. 2017 Mar 6;7(1):79. doi: 10.1038/s41598-017-00152-5. Sci Rep. 2017. PMID: 28250438 Free PMC article.

2

The contribution of human synovial stem cells to skeletal muscle regeneration.

Meng J, Adkin CF, Arechavala-Gomeza V, Boldrin L, Muntoni F, Morgan JE. Meng J, et al. Neuromuscul Disord. 2010 Jan;20(1):6-15. doi: 10.1016/j.nmd.2009.11.007. Neuromuscul Disord. 2010. PMID: 20034794

3

Stem cells to treat muscular dystrophies - where are we?

Meng J, Muntoni F, Morgan JE. Meng J, et al. 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.

4

Contribution of human muscle-derived cells to skeletal muscle regeneration in dystrophic host mice.

Meng J, Adkin CF, Xu SW, Muntoni F, Morgan JE. Meng J, et al. PLoS One. 2011 Mar 9;6(3):e17454. doi: 10.1371/journal.pone.0017454. PLoS One. 2011. PMID: 21408080 Free PMC article.

5

Mouse regenerating myofibers detected as false-positive donor myofibers with anti-human spectrin.

Rozkalne A, Adkin C, Meng J, Lapan A, Morgan JE, Gussoni E. Rozkalne A, et al. Among authors: meng j. Hum Gene Ther. 2014 Jan;25(1):73-81. doi: 10.1089/hum.2013.126. Epub 2013 Dec 19. Hum Gene Ther. 2014. PMID: 24152287 Free PMC article.

6

Human skeletal muscle-derived CD133(+) cells form functional satellite cells after intramuscular transplantation in immunodeficient host mice.

Meng J, Chun S, Asfahani R, Lochmüller H, Muntoni F, Morgan J. Meng J, et al. Mol Ther. 2014 May;22(5):1008-17. doi: 10.1038/mt.2014.26. Epub 2014 Feb 26. Mol Ther. 2014. PMID: 24569833 Free PMC article.

7

The effect of the muscle environment on the regenerative capacity of human skeletal muscle stem cells.

Meng J, Bencze M, Asfahani R, Muntoni F, Morgan JE. Meng J, et al. Skelet Muscle. 2015 Apr 28;5:11. doi: 10.1186/s13395-015-0036-8. eCollection 2015. Skelet Muscle. 2015. PMID: 25949786 Free PMC article.

8

Repeated low doses of morpholino antisense oligomer: an intermediate mouse model of spinal muscular atrophy to explore the window of therapeutic response.

Zhou H, Meng J, Marrosu E, Janghra N, Morgan J, Muntoni F. Zhou H, et al. Among authors: meng j. Hum Mol Genet. 2015 Nov 15;24(22):6265-77. doi: 10.1093/hmg/ddv329. Epub 2015 Aug 11. Hum Mol Genet. 2015. PMID: 26264577 Free PMC article.

9

Autologous skeletal muscle derived cells expressing a novel functional dystrophin provide a potential therapy for Duchenne Muscular Dystrophy.

Meng J, Counsell JR, Reza M, Laval SH, Danos O, Thrasher A, Lochmüller H, Muntoni F, Morgan JE. Meng J, et al. Sci Rep. 2016 Jan 27;6:19750. doi: 10.1038/srep19750. Sci Rep. 2016. PMID: 26813695 Free PMC article.

10

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: meng j. Sci Rep. 2017 Mar 17;7:44775. doi: 10.1038/srep44775. Sci Rep. 2017. PMID: 28303972 Free PMC article.

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