NamiF, BasiriM, SatarianL, et al.Strategies for in vivo genome editing in nondividing cells. Trends Biotechnol, 2018; 36(8):770–786; doi: 10.1016/j.tibtech.2018.03.004
2.
SuzukiK, TsunekawaY, Hernandez-BenitezR, et al.In vivo genome editing via CRISPR/Cas9 mediated homology-independent targeted integration. Nature, 2016; 540(7631):144–149; doi: 10.1038/nature20565
3.
CongL, RanFA, CoxD, et al.Multiplex genome engineering using CRISPR/Cas systems. Science, 2013; 339(6121):819–823; doi: 10.1126/science.1231143
4.
GeisingerJM, StearnsT. CRISPR/Cas9 treatment causes extended TP53-dependent cell cycle arrest in human cells. Nucleic Acids Res, 2020; 48(16):9067–9081; doi: 10.1093/nar/gkaa603
5.
AnzaloneAV, RandolphPB, DavisJR, et al.Search-and-replace genome editing without double-strand breaks or donor DNA. Nature, 2019; 576(7785):149–157; doi: 10.1038/s41586-019-1711-4
6.
AnzaloneAV, GaoXD, PodrackyCJ, et al.Programmable deletion, replacement, integration and inversion of large DNA sequences with twin prime editing. Nat Biotechnol, 2022; 40(5):731–740; doi: 10.1038/s41587-021-01133-w
7.
YarnallMTN, IoannidiEI, Schmitt-UlmsC, et al.Drag-and-drop genome insertion of large sequences without double-strand DNA cleavage using CRISPR-directed integrases. Nat Biotechnol, 2022; doi: 10.1038/s41587-022-01527-4
8.
GrindleyND, WhitesonKL, RicePA. Mechanisms of site-specific recombination. Annu Rev Biochem, 2006; 75(1):567–605; doi: 10.1146/annurev.biochem.73.011303.073908
9.
DurrantMG, FantonA, TyckoJ, et al.Systematic discovery of recombinases for efficient integration of large DNA sequences into the human genome. Nat Biotechnol, 2022; 1–12; doi: 10.1038/s41587-022-01494-w
10.
JusiakB, JagtapK, GaidukovL, et al.Comparison of integrases identifies Bxb1-GA mutant as the most efficient site-specific integrase system in mammalian cells. ACS Synth Biol, 2019; 8(1):16–24; doi: 10.1021/acssynbio.8b00089
11.
WangC, QuY, ChengJK, et al.dCas9-based gene editing for cleavage-free genomic knock-in of long sequences. Nat Cell Biol, 2022; 24(2):268–278; doi: 10.1038/s41556-021-00836-1
