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How CRISPR/Cas9 Gene Editing Is Revolutionizing T Cell Research
Clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 allows for precise gene targeting in mammalian cells, including T cells, allowing scientists to disrupt or edit specific genes of interest. This has enabled immunologists to investigate T cell functions as well as opened the pat...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Mary Ann Liebert, Inc., publishers
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8787706/ https://www.ncbi.nlm.nih.gov/pubmed/34939826 http://dx.doi.org/10.1089/dna.2021.0579 |