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Journal Abstract Search
361 related items for PubMed ID: 17235323
1. 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 [Abstract] [Full Text] [Related]
2. 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. Cell Stem Cell; 2007 Dec 13; 1(6):646-57. PubMed ID: 18371406 [Abstract] [Full Text] [Related]
4. 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 15; 17(16):2507-17. PubMed ID: 18511457 [Abstract] [Full Text] [Related]
10. 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 Aug 15; 11(8):759-67. PubMed ID: 12588108 [Abstract] [Full Text] [Related]
19. 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 15; 18(5):1586-94. PubMed ID: 17314403 [Abstract] [Full Text] [Related]