Homology-directed gene-editing approaches for hematopoietic stem and progenitor cell gene therapy
Abstract The advent of next-generation genome engineering tools like CRISPR-Cas9 has transformed the field of gene therapy, rendering targeted treatment for several incurable diseases. Hematopoietic stem and progenitor cells (HSPCs) continue to be the ideal target cells for gene manipulation due to...
Na minha lista:
| Principais autores: | , , , |
|---|---|
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMC
2021-09-01
|
| coleção: | Stem Cell Research & Therapy |
| Assuntos: | |
| Acesso em linha: | https://doi.org/10.1186/s13287-021-02565-6 |
| Tags: |
Sem tags, seja o primeiro a adicionar uma tag!
|