psPAX2-D64V-NC-MS2 Citations (4)
Originally described in: Delivering SaCas9 mRNA by lentivirus-like bionanoparticles for transient expression and efficient genome editing.Lu B, Javidi-Parsijani P, Makani V, Mehraein-Ghomi F, Sarhan WM, Sun D, Yoo KW, Atala ZP, Lyu P, Atala A Nucleic Acids Res. 2019 Feb 13. pii: 5316732. doi: 10.1093/nar/gkz093. PubMed Journal
Articles Citing psPAX2-D64V-NC-MS2
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| CRISPR/Cas9 increases mitotic gene conversion in human cells. Javidi-Parsijani P, Lyu P, Makani V, Sarhan WM, Yoo KW, El-Korashi L, Atala A, Lu B. Gene Ther. 2020 Jun;27(6):281-296. doi: 10.1038/s41434-020-0126-z. Epub 2020 Feb 4. PubMed |
Engineered cell entry links receptor biology with single-cell genomics.
Yu B, Shi Q, Belk JA, Yost KE, Parker KR, Li R, Liu BB, Huang H, Lingwood D, Greenleaf WJ, Davis MM, Satpathy AT, Chang HY.
Cell. 2022 Dec 22;185(26):4904-4920.e22. doi: 10.1016/j.cell.2022.11.016. Epub 2022 Dec 13.
PubMed
Associated Plasmids |
| Highly efficient cellular expression of circular mRNA enables prolonged protein expression. Unti MJ, Jaffrey SR. bioRxiv. 2023 Jul 11:2023.07.11.548538. doi: 10.1101/2023.07.11.548538. Preprint. PubMed |
Highly efficient cellular expression of circular mRNA enables prolonged protein expression.
Unti MJ, Jaffrey SR.
Cell Chem Biol. 2023 Oct 13:S2451-9456(23)00334-3. doi: 10.1016/j.chembiol.2023.09.015.
PubMed
Associated Plasmids |
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