Cas13b-mediated RNA targeted therapy alleviates genetic dilated cardiomyopathy in mice
Abstract Background Recent advances in gene editing technology have opened up new avenues for in vivo gene therapy, which holds great promise as a potential treatment method for dilated cardiomyopathy (DCM). The CRISPR-Cas13 system has been shown to be an effective tool for knocking down RNA express...
| Published in: | Cell & Bioscience |
|---|---|
| Main Authors: | , , , , , |
| Format: | Article |
| Language: | English |
| Published: |
BMC
2024-01-01
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| Subjects: | |
| Online Access: | https://doi.org/10.1186/s13578-023-01143-y |
