Meng J - Search Results

1

CRISPR-mediated correction of skeletal muscle Ca²⁺ handling in a novel DMD patient-derived pluripotent stem cell model.

Morera C, Kim J, Paredes-Redondo A, Nobles M, Rybin D, Moccia R, Kowala A, Meng J, Garren S, Liu P, Morgan JE, Muntoni F, Christoforou N, Owens J, Tinker A, Lin YY. Morera C, et al. Among authors: meng j. Neuromuscul Disord. 2022 Dec;32(11-12):908-922. doi: 10.1016/j.nmd.2022.10.007. Epub 2022 Nov 1. Neuromuscul Disord. 2022. PMID: 36418198 Free 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

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.

6

CD133+ cells derived from skeletal muscles of Duchenne muscular dystrophy patients have a compromised myogenic and muscle regenerative capability.

Meng J, Muntoni F, Morgan J. Meng J, et al. Stem Cell Res. 2018 Jul;30:43-52. doi: 10.1016/j.scr.2018.05.004. Epub 2018 May 12. Stem Cell Res. 2018. PMID: 29783100 Free PMC article.

7

Effects of Mini-Dystrophin on Dystrophin-Deficient, Human Skeletal Muscle-Derived Cells.

Meng J, Counsell J, Morgan JE. Meng J, et al. Int J Mol Sci. 2020 Sep 28;21(19):7168. doi: 10.3390/ijms21197168. Int J Mol Sci. 2020. PMID: 32998454 Free PMC article.

8

Optogenetic modeling of human neuromuscular circuits in Duchenne muscular dystrophy with CRISPR and pharmacological corrections.

Paredes-Redondo A, Harley P, Maniati E, Ryan D, Louzada S, Meng J, Kowala A, Fu B, Yang F, Liu P, Marino S, Pourquié O, Muntoni F, Wang J, Lieberam I, Lin YY. Paredes-Redondo A, et al. Among authors: meng j. Sci Adv. 2021 Sep 10;7(37):eabi8787. doi: 10.1126/sciadv.abi8787. Epub 2021 Sep 10. Sci Adv. 2021. PMID: 34516770 Free PMC article.

9

Optimized lentiviral vector to restore full-length dystrophin via a cell-mediated approach in a mouse model of Duchenne muscular dystrophy.

Meng J, Moore M, Counsell J, Muntoni F, Popplewell L, Morgan J. Meng J, et al. Mol Ther Methods Clin Dev. 2022 May 2;25:491-507. doi: 10.1016/j.omtm.2022.04.015. eCollection 2022 Jun 9. Mol Ther Methods Clin Dev. 2022. PMID: 35615709 Free PMC article.

10

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.

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