An episomal CRISPR/Cas9 system to derive vector-free gene modified mammalian cells
Linlin Li, Fei Gao, Sen Wu
An episomal CRISPR/Cas9 system to derive vector-free gene modified mammalian cells
[1] |
Cong L, Ran FA, Cox D, Lin S, Barretto R, Habib N, Hsu PD, Wu X, Jiang W, Marraffini LA
CrossRef
Google scholar
|
[2] |
Donsante A, Miller DG, Li Y, Vogler C, Brunt EM, Russell DW, Sands MS (2007) AAV vector integration sites in mouse hepatocellular carcinoma. Science 317:477
CrossRef
Google scholar
|
[3] |
Kouranova E, Forbes K, Zhao G, Warren J, Bartels A, Wu Y, Cui X (2016) CRISPRs for optimal targeting: delivery of CRISPR components as DNA, RNA and protein into cultured cells and single-cell embryos. Hum Gene Ther 27:464–475
CrossRef
Google scholar
|
[4] |
Li H, Malani N, Hamilton SR, Schlachterman A, Bussadori G, Edmonson SE, Shah R, Arruda VR, Mingozzi F, Wright JF
CrossRef
Google scholar
|
[5] |
Lin S, Staahl BT, Alla RK, Doudna JA (2014) Enhanced homologydirected human genome engineering by controlled timing of CRISPR/Cas9 delivery. eLife 3:e04766
CrossRef
Google scholar
|
[6] |
Mali P, Yang L, Esvelt KM, Aach J, Guell M, DiCarlo JE, Norville JE, Church GM (2013) RNA-guided human genome engineering via Cas9. Science 339:823–826
CrossRef
Google scholar
|
[7] |
Nanbo A, Sugden A, Sugden B (2007) The coupling of synthesis and partitioning of EBV's plasmid replicon is revealed in live cells. EMBO J 26:4252–4262
CrossRef
Google scholar
|
[8] |
Okita K, Matsumura Y, Sato Y, Okada A, Morizane A, Okamoto S, Hong H, Nakagawa M, Tanabe K, Tezuka K
CrossRef
Google scholar
|
[9] |
Yin H, Song CQ, Dorkin JR, Zhu LJ, Li Y, Wu Q, Park A, Yang J, Suresh S, Bizhanova A
CrossRef
Google scholar
|
[10] |
Yu JY, Hu KJ, Smuga-Otto K, Tian SL, Stewart R, Slukvin II, Thomson JA (2009) Human induced pluripotent stem cells free of vector and transgene sequences. Science 324:797–801
CrossRef
Google scholar
|
/
〈 | 〉 |