Precision genome editing using combinatorial viral vector delivery of CRISPR-Cas9 nucleases and donor DNA constructs
Zhen Li(Leiden University Medical Center), Manuel A.F.V. Gonçalves(Leiden University)
Cited by 12
Related Papers
In trans paired nicking triggers seamless genome editing without double-stranded DNA cutting
|Nature Communications|2017|91
Broadening the reach and investigating the potential of prime editors through fully viral gene-deleted adenoviral vector delivery
|Nucleic Acids Research|2021|41
High-Capacity Adenoviral Vectors Permit Robust and Versatile Testing of DMD Gene Repair Tools and Strategies in Human Cells
|Cells|2020|26
Selection-free precise gene repair using high-capacity adenovector delivery of advanced prime editing systems rescues dystrophin synthesis in DMD muscle cells
|Nucleic Acids Research|2024|19
Comparative genomic analysis and multilocus sequence typing of Staphylococcus aureus reveals candidate genes for low-temperature tolerance
|The Science of The Total Environment|2024|3