154 related articles for article (PubMed ID: 11054455)
1. Functional EGFP-dystrophin fusion proteins for gene therapy vector development.
Chapdelaine P; Moisset PA; Campeau P; Asselin I; Vilquin JT; Tremblay JP
Protein Eng; 2000 Sep; 13(9):611-5. PubMed ID: 11054455
[TBL] [Abstract][Full Text] [Related]
2. A minidystrophin-EGFP fusion gene expressed in Cos-7 cells mediated by human source vector.
Liang Y; Liang DS; Xue ZG; Long ZG; Wu LQ; Pan Q; Hu YQ; Dai HP; Xia K; Xia JH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Oct; 22(5):493-6. PubMed ID: 16215933
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 17235323
[TBL] [Abstract][Full Text] [Related]
4. Effects of Mini-Dystrophin on Dystrophin-Deficient, Human Skeletal Muscle-Derived Cells.
Meng J; Counsell J; Morgan JE
Int J Mol Sci; 2020 Sep; 21(19):. PubMed ID: 32998454
[TBL] [Abstract][Full Text] [Related]
5. 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(10):1610-22. PubMed ID: 16595609
[TBL] [Abstract][Full Text] [Related]
6. Nucleofection of muscle-derived stem cells and myoblasts with phiC31 integrase: stable expression of a full-length-dystrophin fusion gene by human myoblasts.
Quenneville SP; Chapdelaine P; Rousseau J; Beaulieu J; Caron NJ; Skuk D; Mills P; Olivares EC; Calos MP; Tremblay JP
Mol Ther; 2004 Oct; 10(4):679-87. PubMed ID: 15451452
[TBL] [Abstract][Full Text] [Related]
7. Mini-dystrophin efficiently incorporates into the dystrophin protein complex in living cells.
Draviam RA; Wang B; Li J; Xiao X; Watkins SC
J Muscle Res Cell Motil; 2006; 27(1):53-67. PubMed ID: 16496225
[TBL] [Abstract][Full Text] [Related]
8. Herpes simplex virus type 1 amplicon vector-mediated gene transfer to muscle.
Wang Y; Mukherjee S; Fraefel C; Breakefield XO; Allen PD
Hum Gene Ther; 2002 Jan; 13(2):261-73. PubMed ID: 11812282
[TBL] [Abstract][Full Text] [Related]
9. Transfection of large plasmids in primary human myoblasts.
Campeau P; Chapdelaine P; Seigneurin-Venin S; Massie B; Tremblay JP
Gene Ther; 2001 Sep; 8(18):1387-94. PubMed ID: 11571578
[TBL] [Abstract][Full Text] [Related]
10. Local high-capacity adenovirus-mediated mCTLA4Ig and mCD40Ig expression prolongs recombinant gene expression in skeletal muscle.
Jiang ZL; Reay D; Kreppel F; Gambotto A; Feingold E; Kochanek S; McCarthy SA; Clemens PR
Mol Ther; 2001 Jun; 3(6):892-900. PubMed ID: 11407903
[TBL] [Abstract][Full Text] [Related]
11. Sustained muscle expression of dystrophin from a high-capacity adenoviral vector with systemic gene transfer of T cell costimulatory blockade.
Jiang Z; Schiedner G; van Rooijen N; Liu CC; Kochanek S; Clemens PR
Mol Ther; 2004 Oct; 10(4):688-96. PubMed ID: 15451453
[TBL] [Abstract][Full Text] [Related]
12. Improvement of calcium handling and changes in calcium-release properties after mini- or full-length dystrophin forced expression in cultured skeletal myotubes.
Marchand E; Constantin B; Balghi H; Claudepierre MC; Cantereau A; Magaud C; Mouzou A; Raymond G; Braun S; Cognard C
Exp Cell Res; 2004 Jul; 297(2):363-79. PubMed ID: 15212940
[TBL] [Abstract][Full Text] [Related]
13. Cell-lineage regulated myogenesis for dystrophin replacement: a novel therapeutic approach for treatment of muscular dystrophy.
Kimura E; Han JJ; Li S; Fall B; Ra J; Haraguchi M; Tapscott SJ; Chamberlain JS
Hum Mol Genet; 2008 Aug; 17(16):2507-17. PubMed ID: 18511457
[TBL] [Abstract][Full Text] [Related]
14. Dystrophin expression in host muscle following transplantation of muscle precursor cells modified with the phiC31 integrase.
Quenneville SP; Chapdelaine P; Rousseau J; Tremblay JP
Gene Ther; 2007 Mar; 14(6):514-22. PubMed ID: 17167499
[TBL] [Abstract][Full Text] [Related]
15. Electrotransfer of the full-length dog dystrophin into mouse and dystrophic dog muscles.
Pichavant C; Chapdelaine P; Cerri DG; Bizario JC; Tremblay JP
Hum Gene Ther; 2010 Nov; 21(11):1591-601. PubMed ID: 20553115
[TBL] [Abstract][Full Text] [Related]
16. Herpes simplex virus vector-mediated dystrophin gene transfer and expression in MDX mouse skeletal muscle.
Akkaraju GR; Huard J; Hoffman EP; Goins WF; Pruchnic R; Watkins SC; Cohen JB; Glorioso JC
J Gene Med; 1999; 1(4):280-9. PubMed ID: 10738561
[TBL] [Abstract][Full Text] [Related]
17. 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
Hum Mol Genet; 2006 Jan; 15(2):213-21. PubMed ID: 16321987
[TBL] [Abstract][Full Text] [Related]
18. Herpes simplex virus VP22 enhances adenovirus-mediated microdystrophin gene transfer to skeletal muscles in dystrophin-deficient (mdx) mice.
Xiong F; Xiao S; Peng F; Zheng H; Yu M; Ruan Y; Li W; Shang Y; Zhao C; Zhou W; Chen H; Chamberlain JS; Fang L; Zhang C
Hum Gene Ther; 2007 Jun; 18(6):490-501. PubMed ID: 17550336
[TBL] [Abstract][Full Text] [Related]
19. Expression of truncated dystrophin cDNAs mediated by a lentiviral vector.
Shunchang S; Haitao C; Weidong C; Jingbo H; Yunsheng P
Neurol India; 2008; 56(1):52-6. PubMed ID: 18310838
[TBL] [Abstract][Full Text] [Related]
20. Transgene expression in hypertrophied and aged skeletal muscle in vivo by lentivirus delivery.
Ouyang J; Alway SE
J Gene Med; 2004 Mar; 6(3):278-87. PubMed ID: 15026989
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
