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676 related items for PubMed ID: 12797117
21. Disruption of the splicing enhancer sequence within exon 27 of the dystrophin gene by a nonsense mutation induces partial skipping of the exon and is responsible for Becker muscular dystrophy. Shiga N, Takeshima Y, Sakamoto H, Inoue K, Yokota Y, Yokoyama M, Matsuo M. J Clin Invest; 1997 Nov 01; 100(9):2204-10. PubMed ID: 9410897 [Abstract] [Full Text] [Related]
22. Development of antisense-mediated exon skipping as a treatment for duchenne muscular dystrophy. Heemskerk H, de Winter CL, van Ommen GJ, van Deutekom JC, Aartsma-Rus A. Ann N Y Acad Sci; 2009 Sep 01; 1175():71-9. PubMed ID: 19796079 [Abstract] [Full Text] [Related]
23. Rescue of dystrophin mRNA of Duchenne muscular dystrophy by inducing exon skipping. Matsuo M, Takeshima Y. Acta Myol; 2005 Oct 01; 24(2):110-4. PubMed ID: 16550927 [Abstract] [Full Text] [Related]
24. Specific removal of the nonsense mutation from the mdx dystrophin mRNA using antisense oligonucleotides. Wilton SD, Lloyd F, Carville K, Fletcher S, Honeyman K, Agrawal S, Kole R. Neuromuscul Disord; 1999 Jul 01; 9(5):330-8. PubMed ID: 10407856 [Abstract] [Full Text] [Related]
34. Functional amounts of dystrophin produced by skipping the mutated exon in the mdx dystrophic mouse. Lu QL, Mann CJ, Lou F, Bou-Gharios G, Morris GE, Xue SA, Fletcher S, Partridge TA, Wilton SD. Nat Med; 2003 Aug 01; 9(8):1009-14. PubMed ID: 12847521 [Abstract] [Full Text] [Related]
35. Modulation of in vitro splicing of the upstream intron by modifying an intra-exon sequence which is deleted from the dystrophin gene in dystrophin Kobe. Takeshima Y, Nishio H, Sakamoto H, Nakamura H, Matsuo M. J Clin Invest; 1995 Feb 01; 95(2):515-20. PubMed ID: 7860733 [Abstract] [Full Text] [Related]
36. Design of 2'-O-Me RNA/ENA chimera oligonucleotides to induce exon skipping in dystrophin pre-mRNA. Takagi M, Yagi M, Ishibashi K, Takeshima Y, Surono A, Matsuo M, Koizumi M. Nucleic Acids Symp Ser (Oxf); 2004 Feb 01; (48):297-8. PubMed ID: 17150596 [Abstract] [Full Text] [Related]
40. Efficient bypass of mutations in dysferlin deficient patient cells by antisense-induced exon skipping. Wein N, Avril A, Bartoli M, Beley C, Chaouch S, Laforêt P, Behin A, Butler-Browne G, Mouly V, Krahn M, Garcia L, Lévy N. Hum Mutat; 2010 Feb 01; 31(2):136-42. PubMed ID: 19953532 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]