These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
1295 related items for PubMed ID: 30171539
1. Direct Reprogramming of Human DMD Fibroblasts into Myotubes for In Vitro Evaluation of Antisense-Mediated Exon Skipping and Exons 45-55 Skipping Accompanied by Rescue of Dystrophin Expression. Lee JJA, Saito T, Duddy W, Takeda S, Yokota T. Methods Mol Biol; 2018; 1828():141-150. PubMed ID: 30171539 [Abstract] [Full Text] [Related]
3. Antisense PMO cocktails effectively skip dystrophin exons 45-55 in myotubes transdifferentiated from DMD patient fibroblasts. Lee J, Echigoya Y, Duddy W, Saito T, Aoki Y, Takeda S, Yokota T. PLoS One; 2018; 13(5):e0197084. PubMed ID: 29771942 [Abstract] [Full Text] [Related]
4. Quantitative Antisense Screening and Optimization for Exon 51 Skipping in Duchenne Muscular Dystrophy. Echigoya Y, Lim KRQ, Trieu N, Bao B, Miskew Nichols B, Vila MC, Novak JS, Hara Y, Lee J, Touznik A, Mamchaoui K, Aoki Y, Takeda S, Nagaraju K, Mouly V, Maruyama R, Duddy W, Yokota T. Mol Ther; 2017 Nov 01; 25(11):2561-2572. PubMed ID: 28865998 [Abstract] [Full Text] [Related]
5. Creation of DMD Muscle Cell Model Using CRISPR-Cas9 Genome Editing to Test the Efficacy of Antisense-Mediated Exon Skipping. Maruyama R, Yokota T. Methods Mol Biol; 2018 Nov 01; 1828():165-171. PubMed ID: 30171541 [Abstract] [Full Text] [Related]
8. Antisense PMO found in dystrophic dog model was effective in cells from exon 7-deleted DMD patient. Saito T, Nakamura A, Aoki Y, Yokota T, Okada T, Osawa M, Takeda S. PLoS One; 2010 Aug 18; 5(8):e12239. PubMed ID: 20805873 [Abstract] [Full Text] [Related]
12. In Vivo Evaluation of Multiple Exon Skipping with Peptide-PMOs in Cardiac and Skeletal Muscles in Dystrophic Dogs. Maruyama R, Aoki Y, Takeda S, Yokota T. Methods Mol Biol; 2018 Aug 18; 1828():365-379. PubMed ID: 30171554 [Abstract] [Full Text] [Related]
13. In Vivo Evaluation of Single-Exon and Multiexon Skipping in mdx52 Mice. Mizobe Y, Miyatake S, Takizawa H, Hara Y, Yokota T, Nakamura A, Takeda S, Aoki Y. Methods Mol Biol; 2018 Aug 18; 1828():275-292. PubMed ID: 30171548 [Abstract] [Full Text] [Related]
18. A Dystrophin Exon-52 Deleted Miniature Pig Model of Duchenne Muscular Dystrophy and Evaluation of Exon Skipping. Echigoya Y, Trieu N, Duddy W, Moulton HM, Yin H, Partridge TA, Hoffman EP, Kornegay JN, Rohret FA, Rogers CS, Yokota T. Int J Mol Sci; 2021 Dec 02; 22(23):. PubMed ID: 34884867 [Abstract] [Full Text] [Related]