Similar articles for PMID: 24928536

Year	Number of Results
1991	1
1992	2
1995	1
1996	1
1997	3
1998	2
2000	1
2001	3
2002	1
2003	2
2004	3
2005	4
2006	4
2007	1
2008	5
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2011	4
2012	3
2013	4
2014	6
2015	3
2016	7
2017	4
2018	11
2019	5
2020	7
2021	4
2022	3
2024	0

1

Conserved regions of the DMD 3' UTR regulate translation and mRNA abundance in cultured myotubes.

Larsen CA, Howard MT. Larsen CA, et al. Neuromuscul Disord. 2014 Aug;24(8):693-706. doi: 10.1016/j.nmd.2014.05.006. Epub 2014 May 22. Neuromuscul Disord. 2014. PMID: 24928536 Free PMC article.

2

Molecular characterization of the 5'-UTR of retinal dystrophin reveals a cryptic intron that regulates translational activity.

Kubokawa I, Takeshima Y, Ota M, Enomoto M, Okizuka Y, Mori T, Nishimura N, Awano H, Yagi M, Matsuo M. Kubokawa I, et al. Mol Vis. 2010 Dec 7;16:2590-7. Mol Vis. 2010. PMID: 21151598 Free PMC article.

3

Dual exon skipping in myostatin and dystrophin for Duchenne muscular dystrophy.

Kemaladewi DU, Hoogaars WM, van Heiningen SH, Terlouw S, de Gorter DJ, den Dunnen JT, van Ommen GJ, Aartsma-Rus A, ten Dijke P, 't Hoen PA. Kemaladewi DU, et al. BMC Med Genomics. 2011 Apr 20;4:36. doi: 10.1186/1755-8794-4-36. BMC Med Genomics. 2011. PMID: 21507246 Free PMC article.

4

Skeletal Muscle Differentiation on a Chip Shows Human Donor Mesoangioblasts' Efficiency in Restoring Dystrophin in a Duchenne Muscular Dystrophy Model.

Serena E, Zatti S, Zoso A, Lo Verso F, Tedesco FS, Cossu G, Elvassore N. Serena E, et al. Stem Cells Transl Med. 2016 Dec;5(12):1676-1683. doi: 10.5966/sctm.2015-0053. Epub 2016 Aug 8. Stem Cells Transl Med. 2016. PMID: 27502519 Free PMC article.

5

Antisense-induced exon skipping restores dystrophin expression in DMD patient derived muscle cells.

van Deutekom JC, Bremmer-Bout M, Janson AA, Ginjaar IB, Baas F, den Dunnen JT, van Ommen GJ. van Deutekom JC, et al. Hum Mol Genet. 2001 Jul 15;10(15):1547-54. doi: 10.1093/hmg/10.15.1547. Hum Mol Genet. 2001. PMID: 11468272

6

Human multipotent adipose-derived stem cells restore dystrophin expression of Duchenne skeletal-muscle cells in vitro.

Vieira NM, Brandalise V, Zucconi E, Jazedje T, Secco M, Nunes VA, Strauss BE, Vainzof M, Zatz M. Vieira NM, et al. Biol Cell. 2008 Apr;100(4):231-41. doi: 10.1042/BC20070102. Biol Cell. 2008. PMID: 17997718

7

Direct Reprogramming of Human DMD Fibroblasts into Myotubes for In Vitro Evaluation of Antisense-Mediated Exon Skipping and Exons 45-55 Skipping Accompanied by Rescue of Dystrophin Expression.

Lee JJA, Saito T, Duddy W, Takeda S, Yokota T. Lee JJA, et al. Methods Mol Biol. 2018;1828:141-150. doi: 10.1007/978-1-4939-8651-4_8. Methods Mol Biol. 2018. PMID: 30171539 Free PMC article.

8

Human mesenchymal stem cells ectopically expressing full-length dystrophin can complement Duchenne muscular dystrophy myotubes by cell fusion.

Gonçalves MA, de Vries AA, Holkers M, van de Watering MJ, van der Velde I, van Nierop GP, Valerio D, Knaän-Shanzer S. Gonçalves MA, et al. Hum Mol Genet. 2006 Jan 15;15(2):213-21. doi: 10.1093/hmg/ddi438. Epub 2005 Dec 1. Hum Mol Genet. 2006. PMID: 16321987

9

Characterization of a Dmd (EGFP) reporter mouse as a tool to investigate dystrophin expression.

Petkova MV, Morales-Gonzales S, Relizani K, Gill E, Seifert F, Radke J, Stenzel W, Garcia L, Amthor H, Schuelke M. Petkova MV, et al. Skelet Muscle. 2016 Jul 5;6:25. doi: 10.1186/s13395-016-0095-5. eCollection 2016. Skelet Muscle. 2016. PMID: 27382459 Free PMC article.

10

De novo revertant fiber formation and therapy testing in a 3D culture model of Duchenne muscular dystrophy skeletal muscle.

Ebrahimi M, Lad H, Fusto A, Tiper Y, Datye A, Nguyen CT, Jacques E, Moyle LA, Nguyen T, Musgrave B, Chávez-Madero C, Bigot A, Chen C, Turner S, Stewart BA, Pegoraro E, Vitiello L, Gilbert PM. Ebrahimi M, et al. Acta Biomater. 2021 Sep 15;132:227-244. doi: 10.1016/j.actbio.2021.05.020. Epub 2021 May 25. Acta Biomater. 2021. PMID: 34048976

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