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Items: 1 to 20 of 87

1.

Cell therapies for muscular dystrophy.

Blau HM.

N Engl J Med. 2008 Sep 25;359(13):1403-5. doi: 10.1056/NEJMcibr0805708. No abstract available.

PMID:
18815403
2.

Mural cells paint a new picture of muscle stem cells.

Morgan J, Muntoni F.

Nat Cell Biol. 2007 Mar;9(3):249-51. No abstract available.

PMID:
17330116
3.

Stem-cell biology: a move in the right direction.

Chamberlain JS.

Nature. 2006 Nov 30;444(7119):552-3. No abstract available.

PMID:
17108968
4.

[Future treatment modalities in Duchenne muscular dystrophy].

Oron A, Shuper A, Shohat M.

Harefuah. 1998 Apr 1;134(7):557-60. Review. Hebrew. No abstract available.

PMID:
10909603
5.

Mdx mice inducibly expressing dystrophin provide insights into the potential of gene therapy for duchenne muscular dystrophy.

Ahmad A, Brinson M, Hodges BL, Chamberlain JS, Amalfitano A.

Hum Mol Genet. 2000 Oct 12;9(17):2507-15.

PMID:
11030755
6.

Menstrual blood-derived cells confer human dystrophin expression in the murine model of Duchenne muscular dystrophy via cell fusion and myogenic transdifferentiation.

Cui CH, Uyama T, Miyado K, Terai M, Kyo S, Kiyono T, Umezawa A.

Mol Biol Cell. 2007 May;18(5):1586-94.

PMID:
17314403
7.

[Restoration of human dystrophin following transplantation of exon-skipping-engineered DMD patient stem cells into dystrophic mice].

Benchaouir R, Meregalli M, Farini A, D'Antona G, Belicchi M, Goyenvalle A, Battistelli M, Bresolin N, Bottinelli R, Garcia L, Torrente Y.

Med Sci (Paris). 2008 Jan;24(1):99-101. doi: 10.1051/medsci/200824199. French. No abstract available.

PMID:
18198122
8.

A highly functional mini-dystrophin/GFP fusion gene for cell and gene therapy studies of Duchenne muscular dystrophy.

Li S, Kimura E, Ng R, Fall BM, Meuse L, Reyes M, Faulkner JA, Chamberlain JS.

Hum Mol Genet. 2006 May 15;15(10):1610-22.

PMID:
16595609
9.

Splice modification to restore functional dystrophin synthesis in Duchenne muscular dystrophy.

Wilton SD, Fletcher S.

Curr Pharm Des. 2010;16(8):988-1001. Review.

PMID:
20041827
10.

Autologous transplantation of muscle precursor cells modified with a lentivirus for muscular dystrophy: human cells and primate models.

Quenneville SP, Chapdelaine P, Skuk D, Paradis M, Goulet M, Rousseau J, Xiao X, Garcia L, Tremblay JP.

Mol Ther. 2007 Feb;15(2):431-8.

PMID:
17235323
11.

Systemic delivery of allogenic muscle stem cells induces long-term muscle repair and clinical efficacy in duchenne muscular dystrophy dogs.

Rouger K, Larcher T, Dubreil L, Deschamps JY, Le Guiner C, Jouvion G, Delorme B, Lieubeau B, Carlus M, Fornasari B, Theret M, Orlando P, Ledevin M, Zuber C, Leroux I, Deleau S, Guigand L, Testault I, Le Rumeur E, Fiszman M, Chérel Y.

Am J Pathol. 2011 Nov;179(5):2501-18. doi: 10.1016/j.ajpath.2011.07.022.

PMID:
21924229
12.

Autotransplantation in mdx mice of mdx myoblasts genetically corrected by an HSV-1 amplicon vector.

Bujold M, Caron N, Camiran G, Mukherjee S, Allen PD, Tremblay JP, Wang Y.

Cell Transplant. 2002;11(8):759-67.

PMID:
12588108
13.

The role of utrophin in the potential therapy of Duchenne muscular dystrophy.

Perkins KJ, Davies KE.

Neuromuscul Disord. 2002 Oct;12 Suppl 1:S78-89. Review.

PMID:
12206801
14.

Cell transplantation and gene therapy in muscular dystrophy.

Morgan JE, Partridge TA.

Bioessays. 1992 Sep;14(9):641-5.

PMID:
1365921
15.

Restoration of muscle fibers and satellite cells after isogenic MSC transplantation with microdystrophin gene delivery.

Feng SW, Chen F, Cao J, Yu MJ, Liang YY, Song XM, Zhang C.

Biochem Biophys Res Commun. 2012 Mar 2;419(1):1-6. doi: 10.1016/j.bbrc.2012.01.029.

PMID:
22321394
16.
17.

Identification of a putative pathway for the muscle homing of stem cells in a muscular dystrophy model.

Torrente Y, Camirand G, Pisati F, Belicchi M, Rossi B, Colombo F, El Fahime M, Caron NJ, Issekutz AC, Constantin G, Tremblay JP, Bresolin N.

J Cell Biol. 2003 Aug 4;162(3):511-20.

PMID:
12885758
18.

[Stem cell based cell therapy for muscular dystrophy].

Takeda S.

Rinsho Shinkeigaku. 2006 Nov;46(11):945-8. Japanese.

PMID:
17432228
19.

Full-length dystrophin cDNA transfer into skeletal muscle of adult mdx mice by electroporation.

Murakami T, Nishi T, Kimura E, Goto T, Maeda Y, Ushio Y, Uchino M, Sunada Y.

Muscle Nerve. 2003 Feb;27(2):237-41.

PMID:
12548532
20.

Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs.

Sampaolesi M, Blot S, D'Antona G, Granger N, Tonlorenzi R, Innocenzi A, Mognol P, Thibaud JL, Galvez BG, Barthélémy I, Perani L, Mantero S, Guttinger M, Pansarasa O, Rinaldi C, Cusella De Angelis MG, Torrente Y, Bordignon C, Bottinelli R, Cossu G.

Nature. 2006 Nov 30;444(7119):574-9. Erratum in: Nature. 2014 Mar 13;507(7491):262. Nature. 2013 Feb 28;494(7438):506.

PMID:
17108972
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