pCMV-PE7 Citations (4)
Originally described in: Improving prime editing with an endogenous small RNA-binding protein.Yan J, Oyler-Castrillo P, Ravisankar P, Ward CC, Levesque S, Jing Y, Simpson D, Zhao A, Li H, Yan W, Goudy L, Schmidt R, Solley SC, Gilbert LA, Chan MM, Bauer DE, Marson A, Parsons LR, Adamson B Nature. 2024 Apr 3. doi: 10.1038/s41586-024-07259-6. PubMed Journal
Articles Citing pCMV-PE7
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| Pan-cancer analysis of biallelic inactivation in tumor suppressor genes identifies KEAP1 zygosity as a predictive biomarker in lung cancer. Zucker M, Perry MA, Gould SI, Elkrief A, Safonov A, Thummalapalli R, Mehine M, Chakravarty D, Brannon AR, Ladanyi M, Razavi P, Donoghue MTA, Murciano-Goroff YR, Grigoriadis K, McGranahan N, Jamal-Hanjani M, Swanton C, Chen Y, Shen R, Chandarlapaty S, Solit DB, Schultz N, Berger MF, Chang J, Schoenfeld AJ, Sanchez-Rivera FJ, Reznik E, Bandlamudi C. Cell. 2025 Feb 6;188(3):851-867.e17. doi: 10.1016/j.cell.2024.11.010. Epub 2024 Dec 18. PubMed |
| Precise Generation of Human Induced Pluripotent Stem Cell-derived Cell Lines Harboring Disease-relevant Single Nucleotide Variants Using a Prime Editing System. Kanno S, Sato K, Nakazawa T. Bio Protoc. 2025 Feb 20;15(4):e5191. doi: 10.21769/BioProtoc.5191. eCollection 2025 Feb 20. PubMed |
| Precise Correction of the Pde6b-L659P Mutation Causing Retinal Degeneration with Minimum Bystander Editing by Advanced Genome Editing Tools. Liu Z, Chen S, Sun Y. Research (Wash D C). 2025 Jul 2;8:0770. doi: 10.34133/research.0770. eCollection 2025. PubMed |
| Investigating and correcting a rare pathogenic mutation in GDF11. Congdon ST, Bennett J, Opinya R, Agosto AR, Dossias O, Kokko C, Levesque AA, Koob AO, Silver AC, Thomas-Charles CA. HGG Adv. 2026 Jan 15;7(1):100559. doi: 10.1016/j.xhgg.2025.100559. Epub 2025 Dec 18. PubMed |
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