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Results: 1 to 20 of 86

Similar articles for PubMed (Select 22303359)

1.

Dystrophin Orchestrates the Epigenetic Profile of Muscle Cells Via miRNAs.

Marrone AK, Shcherbata HR.

Front Genet. 2011 Sep 13;2:64. doi: 10.3389/fgene.2011.00064. eCollection 2011.

2.

Dg-Dys-Syn1 signaling in Drosophila regulates the microRNA profile.

Marrone AK, Edeleva EV, Kucherenko MM, Hsiao NH, Shcherbata HR.

BMC Cell Biol. 2012 Oct 29;13:26. doi: 10.1186/1471-2121-13-26.

3.

MicroRNAs involved in molecular circuitries relevant for the Duchenne muscular dystrophy pathogenesis are controlled by the dystrophin/nNOS pathway.

Cacchiarelli D, Martone J, Girardi E, Cesana M, Incitti T, Morlando M, Nicoletti C, Santini T, Sthandier O, Barberi L, Auricchio A, Musarò A, Bozzoni I.

Cell Metab. 2010 Oct 6;12(4):341-51. doi: 10.1016/j.cmet.2010.07.008. Epub 2010 Aug 19.

4.

Identification of muscle-specific microRNAs in serum of muscular dystrophy animal models: promising novel blood-based markers for muscular dystrophy.

Mizuno H, Nakamura A, Aoki Y, Ito N, Kishi S, Yamamoto K, Sekiguchi M, Takeda S, Hashido K.

PLoS One. 2011 Mar 30;6(3):e18388. doi: 10.1371/journal.pone.0018388.

5.
6.

Complete genetic correction of ips cells from Duchenne muscular dystrophy.

Kazuki Y, Hiratsuka M, Takiguchi M, Osaki M, Kajitani N, Hoshiya H, Hiramatsu K, Yoshino T, Kazuki K, Ishihara C, Takehara S, Higaki K, Nakagawa M, Takahashi K, Yamanaka S, Oshimura M.

Mol Ther. 2010 Feb;18(2):386-93. doi: 10.1038/mt.2009.274. Epub 2009 Dec 8.

7.

Temporal gene expression profiling of dystrophin-deficient (mdx) mouse diaphragm identifies conserved and muscle group-specific mechanisms in the pathogenesis of muscular dystrophy.

Porter JD, Merriam AP, Leahy P, Gong B, Feuerman J, Cheng G, Khanna S.

Hum Mol Genet. 2004 Feb 1;13(3):257-69. Epub 2003 Dec 17.

8.

Application of microRNA in cardiac and skeletal muscle disease gene therapy.

Huang ZP, Neppl RL Jr, Wang DZ.

Methods Mol Biol. 2011;709:197-210. doi: 10.1007/978-1-61737-982-6_12.

PMID:
21194029
9.

Dystrophins carrying spectrin-like repeats 16 and 17 anchor nNOS to the sarcolemma and enhance exercise performance in a mouse model of muscular dystrophy.

Lai Y, Thomas GD, Yue Y, Yang HT, Li D, Long C, Judge L, Bostick B, Chamberlain JS, Terjung RL, Duan D.

J Clin Invest. 2009 Mar;119(3):624-35. doi: 10.1172/JCI36612. Epub 2009 Feb 23.

10.
11.

A web-accessible complete transcriptome of normal human and DMD muscle.

Bakay M, Zhao P, Chen J, Hoffman EP.

Neuromuscul Disord. 2002 Oct;12 Suppl 1:S125-41.

PMID:
12206807
12.

Muscle regeneration in dystrophin-deficient mdx mice studied by gene expression profiling.

Turk R, Sterrenburg E, de Meijer EJ, van Ommen GJ, den Dunnen JT, 't Hoen PA.

BMC Genomics. 2005 Jul 13;6:98.

13.

Common micro-RNA signature in skeletal muscle damage and regeneration induced by Duchenne muscular dystrophy and acute ischemia.

Greco S, De Simone M, Colussi C, Zaccagnini G, Fasanaro P, Pescatori M, Cardani R, Perbellini R, Isaia E, Sale P, Meola G, Capogrossi MC, Gaetano C, Martelli F.

FASEB J. 2009 Oct;23(10):3335-46. doi: 10.1096/fj.08-128579. Epub 2009 Jun 15.

14.

Stem cell therapies to treat muscular dystrophy: progress to date.

Meregalli M, Farini A, Parolini D, Maciotta S, Torrente Y.

BioDrugs. 2010 Aug 1;24(4):237-47. doi: 10.2165/11534300-000000000-00000. Review.

PMID:
20623990
15.

Function and genetics of dystrophin and dystrophin-related proteins in muscle.

Blake DJ, Weir A, Newey SE, Davies KE.

Physiol Rev. 2002 Apr;82(2):291-329. Review.

16.

Multiple regulatory events controlling the expression and localization of utrophin in skeletal muscle fibers: insights into a therapeutic strategy for Duchenne muscular dystrophy.

Jasmin BJ, Angus LM, Bélanger G, Chakkalakal JV, Gramolini AO, Lunde JA, Stocksley MA, Thompson J.

J Physiol Paris. 2002 Jan-Mar;96(1-2):31-42. Review.

PMID:
11755781
17.

Absence of neuronal nitric oxide synthase (nNOS) as a pathological marker for the diagnosis of Becker muscular dystrophy with rod domain deletions.

Torelli S, Brown SC, Jimenez-Mallebrera C, Feng L, Muntoni F, Sewry CA.

Neuropathol Appl Neurobiol. 2004 Oct;30(5):540-5.

PMID:
15488030
18.

[Association between dystrophin and neuronal nitric oxide synthase in muscles of progressive muscular dystrophy].

Wang S, Shen D.

Zhonghua Yi Xue Za Zhi. 2002 Feb 10;82(3):155-7. Chinese.

PMID:
11953148
19.
20.

Transcriptional profiles from patients with dystrophinopathies and limb girdle muscular dystrophies as determined by qRT-PCR.

Arning L, Jagiello P, Schara U, Vorgerd M, Dahmen N, Gencikova A, Mortier W, Epplen JT, Gencik M.

J Neurol. 2004 Jan;251(1):72-8.

PMID:
14999492
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