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肌肉萎缩症基因治疗新方法
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Science：全新基因治疗新方法——将大基因分两部分传递给患者
https://www.ebiotrade.com/newsf/2024-11/20241115045510143.htm
http://www.pubmedplus.cn/P/SearchQuickResult?wd=9b136bcf-1a78-4184-9211-ee629c816ab3
| 01. | RNA, Catalytic | 83 篇 | 83.000% |
| 02. | RNA, Messenger | 66 篇 | 66.000% |
| 03. | Humans | 59 篇 | 59.000% |
| 04. | Base Sequence | 49 篇 | 49.000% |
| 05. | Animals | 44 篇 | 44.000% |
| 06. | Genetic Vectors | 44 篇 | 44.000% |
| 07. | Genetic Therapy | 39 篇 | 39.000% |
| 08. | Molecular Sequence Data | 39 篇 | 39.000% |
| 09. | Nucleic Acid Conformation | 31 篇 | 31.000% |
| 10. | Mice | 28 篇 | 28.000% |
1. Ribozyme-activated mRNA trans-ligation enables large gene delivery to treat muscular dystrophies.
Aab Cardiovascular Research Institute, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA.
Science (P 1095-9203 E 0036-8075) 2024 年 386 卷 6723 期 762-767 页
PMID：39541470 相似文献
2. Stitchr: stitching coding TCR nucleotide sequences from V/J/CDR3 information.
Massachusetts General Hospital Cancer Center, Charlestown, MA, USA.
Nucleic Acids Res (P 1362-4962 E 0305-1048) H指数：452 2022 年 50 卷 12 期 e68 页
PMID：35325179 相似文献
https://blog.sciencenet.cn/blog-280034-1460509.html
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