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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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Detalles Bibliográficos
Autor principal:	Johansen, Kristoffer Haurum
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Mary Ann Liebert, Inc., publishers 2022
Materias:	Section C: Synergy of New Technologies with Basic and Translational Research
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

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