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Gene-mediated restoration of normal myofiber elasticity in dystrophic muscles.
Mol Ther. 2009 Jan;17(1):19-25. doi: 10.1038/mt.2008.239. Epub 2008 Nov 11.
2
Combined effect of AAV-U7-induced dystrophin exon skipping and soluble activin Type IIB receptor in mdx mice.
Hum Gene Ther. 2012 Dec;23(12):1269-79. doi: 10.1089/hum.2012.056. Epub 2012 Sep 24.
3
Muscle function recovery in golden retriever muscular dystrophy after AAV1-U7 exon skipping.
Mol Ther. 2012 Nov;20(11):2120-33. doi: 10.1038/mt.2012.181. Epub 2012 Sep 11.
5
AAV genome loss from dystrophic mouse muscles during AAV-U7 snRNA-mediated exon-skipping therapy.
Mol Ther. 2013 Aug;21(8):1551-8. doi: 10.1038/mt.2013.121. Epub 2013 Jun 11.
6
Rescue of dystrophic muscle through U7 snRNA-mediated exon skipping.
Science. 2004 Dec 3;306(5702):1796-9. doi: 10.1126/science.1104297. Epub 2004 Nov 4.
7
Antisense pre-treatment increases gene therapy efficacy in dystrophic muscles.
Hum Mol Genet. 2016 Aug 15;25(16):3555-3563. doi: 10.1093/hmg/ddw201. Epub 2016 Jul 4.
8
Dystrophin Gene-Editing Stability Is Dependent on Dystrophin Levels in Skeletal but Not Cardiac Muscles.
Mol Ther. 2021 Mar 3;29(3):1070-1085. doi: 10.1016/j.ymthe.2020.11.003. Epub 2020 Nov 5.
10
rAAV6-microdystrophin preserves muscle function and extends lifespan in severely dystrophic mice.
Nat Med. 2006 Jul;12(7):787-9. doi: 10.1038/nm1439. Epub 2006 Jul 2.

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Expression of Myomaker and Myomerger in myofibers causes muscle pathology.
Skelet Muscle. 2023 May 1;13(1):8. doi: 10.1186/s13395-023-00317-z.
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Three-dimensional mechanical characterization of murine skeletal muscle using quantitative micro-elastography.
Biomed Opt Express. 2022 Oct 17;13(11):5879-5899. doi: 10.1364/BOE.471062. eCollection 2022 Nov 1.
4
Exon skipping induces uniform dystrophin rescue with dose-dependent restoration of serum miRNA biomarkers and muscle biophysical properties.
Mol Ther Nucleic Acids. 2022 Aug 25;29:955-968. doi: 10.1016/j.omtn.2022.08.033. eCollection 2022 Sep 13.
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Nanomechanics in Monitoring the Effectiveness of Drugs Targeting the Cancer Cell Cytoskeleton.
Int J Mol Sci. 2020 Nov 20;21(22):8786. doi: 10.3390/ijms21228786.
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An AFM-Based Nanomechanical Study of Ovarian Tissues with Pathological Conditions.
Int J Nanomedicine. 2020 Jun 19;15:4333-4350. doi: 10.2147/IJN.S254342. eCollection 2020.
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Fibrogenesis in -Related Muscular Dystrophy Is a Central Tenet of Disease Etiology.
Front Mol Neurosci. 2020 Feb 4;13:3. doi: 10.3389/fnmol.2020.00003. eCollection 2020.
9
Myotube elasticity of an amyotrophic lateral sclerosis mouse model.
Sci Rep. 2018 Apr 12;8(1):5917. doi: 10.1038/s41598-018-24027-5.
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Autologous Cell Therapy Approach for Duchenne Muscular Dystrophy using PiggyBac Transposons and Mesoangioblasts.
Mol Ther. 2018 Apr 4;26(4):1093-1108. doi: 10.1016/j.ymthe.2018.01.021. Epub 2018 Feb 2.

本文引用的文献

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Investigation of Debio 025, a cyclophilin inhibitor, in the dystrophic mdx mouse, a model for Duchenne muscular dystrophy.
Br J Pharmacol. 2008 Oct;155(4):574-84. doi: 10.1038/bjp.2008.285. Epub 2008 Jul 21.
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Muscle diseases: the muscular dystrophies.
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Stiffness alterations of single cells induced by UV in the presence of nanoTiO2.
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Green fluorescent protein impairs actin-myosin interactions by binding to the actin-binding site of myosin.
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Mesenchymal stem cell injection after myocardial infarction improves myocardial compliance.
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Utrophin upregulation for treating Duchenne or Becker muscular dystrophy: how close are we?
Trends Mol Med. 2006 Mar;12(3):122-9. doi: 10.1016/j.molmed.2006.01.002. Epub 2006 Jan 27.
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Rescue of dystrophic muscle through U7 snRNA-mediated exon skipping.
Science. 2004 Dec 3;306(5702):1796-9. doi: 10.1126/science.1104297. Epub 2004 Nov 4.

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