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Journal Abstract Search
178 related items for PubMed ID: 10455444
1. Enhanced expression of recombinant dystrophin following intramuscular injection of Epstein-Barr virus (EBV)-based mini-chromosome vectors in mdx mice. Tsukamoto H, Wells D, Brown S, Serpente P, Strong P, Drew J, Inui K, Okada S, Dickson G. Gene Ther; 1999 Jul; 6(7):1331-5. PubMed ID: 10455444 [Abstract] [Full Text] [Related]
2. Full-length dystrophin gene transfer to the mdx mouse in utero. Reay DP, Bilbao R, Koppanati BM, Cai L, O'Day TL, Jiang Z, Zheng H, Watchko JF, Clemens PR. Gene Ther; 2008 Apr; 15(7):531-6. PubMed ID: 18273052 [Abstract] [Full Text] [Related]
3. Restoration of dystrophin expression in mdx mice by intravascular injection of naked DNA containing full-length dystrophin cDNA. Liang KW, Nishikawa M, Liu F, Sun B, Ye Q, Huang L. Gene Ther; 2004 Jun; 11(11):901-8. PubMed ID: 14985786 [Abstract] [Full Text] [Related]
4. Transfer of full-length Dmd to the diaphragm muscle of Dmd(mdx/mdx) mice through systemic administration of plasmid DNA. Liu F, Nishikawa M, Clemens PR, Huang L. Mol Ther; 2001 Jul; 4(1):45-51. PubMed ID: 11472105 [Abstract] [Full Text] [Related]
6. Highly efficient gene transfer into murine liver achieved by intravenous administration of naked Epstein-Barr virus (EBV)-based plasmid vectors. Cui FD, Kishida T, Ohashi S, Asada H, Yasutomi K, Satoh E, Kubo T, Fushiki S, Imanishi J, Mazda O. Gene Ther; 2001 Oct; 8(19):1508-13. PubMed ID: 11593364 [Abstract] [Full Text] [Related]
7. 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. PubMed ID: 12548532 [Abstract] [Full Text] [Related]
14. Comparison of high-capacity and first-generation adenoviral vector gene delivery to murine muscle in utero. Bilbao R, Reay DP, Wu E, Zheng H, Biermann V, Kochanek S, Clemens PR. Gene Ther; 2005 Jan; 12(1):39-47. PubMed ID: 15483668 [Abstract] [Full Text] [Related]
15. Enhanced effect of microdystrophin gene transfection by HSV-VP22 mediated intercellular protein transport. Xiong F, Xiao S, Yu M, Li W, Zheng H, Shang Y, Peng F, Zhao C, Zhou W, Chen H, Fang L, Chamberlain JS, Zhang C. BMC Neurosci; 2007 Jul 08; 8():50. PubMed ID: 17617925 [Abstract] [Full Text] [Related]
16. A canine minidystrophin is functional and therapeutic in mdx mice. Wang B, Li J, Qiao C, Chen C, Hu P, Zhu X, Zhou L, Bogan J, Kornegay J, Xiao X. Gene Ther; 2008 Aug 08; 15(15):1099-106. PubMed ID: 18432277 [Abstract] [Full Text] [Related]
17. AAV vector-mediated microdystrophin expression in a relatively small percentage of mdx myofibers improved the mdx phenotype. Yoshimura M, Sakamoto M, Ikemoto M, Mochizuki Y, Yuasa K, Miyagoe-Suzuki Y, Takeda S. Mol Ther; 2004 Nov 08; 10(5):821-8. PubMed ID: 15509500 [Abstract] [Full Text] [Related]
18. Local and distant transfection of mdx muscle fibers with dystrophin and LacZ genes delivered in vivo by synthetic microspheres. Baranov A, Glazkov P, Kiselev A, Ostapenko O, Mikhailov V, Ivaschenko T, Sabetsky V, Baranov V. Gene Ther; 1999 Aug 08; 6(8):1406-14. PubMed ID: 10467365 [Abstract] [Full Text] [Related]
19. Epstein-Barr virus vectors provide prolonged robust factor IX expression in mice. Sclimenti CR, Neviaser AS, Baba EJ, Meuse L, Kay MA, Calos MP. Biotechnol Prog; 2003 Aug 08; 19(1):144-51. PubMed ID: 12573017 [Abstract] [Full Text] [Related]
20. Design of trans-splicing adeno-associated viral vectors for Duchenne muscular dystrophy gene therapy. Lai Y, Li D, Yue Y, Duan D. Methods Mol Biol; 2008 Aug 08; 433():259-75. PubMed ID: 18679629 [Abstract] [Full Text] [Related] Page: [Next] [New Search]