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| Format: | Recurso digital |
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Zenodo
2025
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| Online Access: | https://doi.org/10.5281/zenodo.14915505 |
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Table of Contents:
- <p>The goal of this project is to design a series of CRISPR-based vaccines aimed at<br>addressing a wide range of genetic diseases. These vaccines will be designed<br>to:<br>● Eliminate the genetic mutations responsible for conditions such as cystic<br>fibrosis, gigantism, Down syndrome, sickle cell anemia, among others.<br>● Correct or replace defective genes that cause these disorders through<br>precise genetic editing.<br>● Add therapeutic genes that promote tissue regeneration, helping repair<br>damage caused by these diseases at the cellular and tissue levels.<br>These vaccines will not only correct the underlying cause of these diseases but<br>will also enhance the body's ability to repair and regenerate tissues and organs<br>damaged by genetic mutations</p>