p53 Hinders CRISPR/Cas9-Mediated Targeted Gene Disruption in Memory CD8 T Cells In Vivo
Author:
Publisher
The American Association of Immunologists
Subject
Immunology,Immunology and Allergy
Reference49 articles.
1. The next generation of CRISPR-Cas technologies and applications.;Pickar-Oliver;Nat. Rev. Mol. Cell Biol.,2019
2. The Functional Requirement for CD69 in Establishment of Resident Memory CD8+T Cells Varies with Tissue Location
3. Optimized RNP transfection for highly efficient CRISPR/Cas9-mediated gene knockout in primary T cells
4. CRISPR–Cas9 genome engineering of primary CD4+ T cells for the interrogation of HIV–host factor interactions
5. Generation of knock-in primary human T cells using Cas9 ribonucleoproteins
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1. Increasing Gene Editing Efficiency via CRISPR/Cas9- or Cas12a-Mediated Knock-In in Primary Human T Cells;Biomedicines;2024-01-06
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3. Molecular dynamics of genome editing with CRISPR-Cas9 and rAAV6 virus in human HSPCs to treat sickle cell disease;Molecular Therapy - Methods & Clinical Development;2023-09
4. Sublethal whole-body irradiation induces permanent loss and dysfunction in pathogen-specific circulating memory CD8 T cell populations;Proceedings of the National Academy of Sciences;2023-06-26
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