Rapid and Efficient Gene Editing for Direct Transplantation of Naive Murine Cas9(+) T Cells

Gene editing of primary T cells is a difficult task. However, it is important for research and especially for clinical T-cell transfers. CRISPR/Cas9 is the most powerful gene-editing technique. It has to be applied to cells by either retroviral transduction or electroporation of ribonucleoprotein co...

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Detalles Bibliográficos
Autores principales: Majumder, Snigdha, Jugovic, Isabelle, Saul, Domenica, Bell, Luisa, Hundhausen, Nadine, Seal, Rishav, Beilhack, Andreas, Rosenwald, Andreas, Mougiakakos, Dimitrios, Berberich-Siebelt, Friederike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8335400/
https://www.ncbi.nlm.nih.gov/pubmed/34367143
http://dx.doi.org/10.3389/fimmu.2021.683631

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8335400/
https://www.ncbi.nlm.nih.gov/pubmed/34367143
http://dx.doi.org/10.3389/fimmu.2021.683631

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