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From DNA break repair pathways to CRISPR/Cas-mediated gene knock-in methods.
Plasmid-Based Donor Templates for Nonviral CRISPR/Cas9-Mediated Gene Knock-In in Human T Cells.
An efficient gene knock-in strategy using 5'-modified double-stranded DNA donors with short homology…
Reporter gene knock-in into Marc-145 cells using CRISPR/Cas9-mediated homologous recombination.
Single-Copy Knock-In Loci for Defined Gene Expression in Caenorhabditis elegans.
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Study of CRISPR-Cas9 Mediated PD-1 and TCR Gene-knocked Out Mesothelin-directed CAR-T Cells in Patie…
Study of PD-1 Gene-knocked Out Mesothelin-directed CAR-T Cells With the Conditioning of PC in Mesoth…
Gene Transfer Therapy for Treating Children and Adults With Limb Girdle Muscular Dystrophy Type 2D (…
Differential Gene Expression of Liver Tissue and Blood From Individuals With Chronic Viral Hepatitis
CRISPR/Cas9-modified Human T Cell ( PD-1and ACE2 Knockout Engineered T Cells ) for Inducing Long-ter…
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