Artificial Virus Delivers CRISPR-Cas9 System for Genome Editing of Cells in Mice

Li, Ling, Song, Linjiang, Liu, Xiaowei, Yang, Xi, Li, Xia, He, Tao, Wang, Ning, Yang, Suleixin +10 more·2017·ACS Nano

Cited by (245)

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  8. Convergent Arrangement of sgRNA and Cas9 in CRISPRsome for Transcellular Trafficking
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  9. Polymer-Mediated Delivery of CRISPR-Cas9 Genome-Editing Therapeutics for CNS Disease
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  10. Key to Delivery: The (Epi-)genome Editing Vector Toolbox
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  14. Human germline editing: Insights to future clinical treatment of diseases
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  15. Advancements of CRISPR/Cas9 technology and its value in antiviral therapeutics
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  16. Single-cell transcriptomics reveals the mechanisms of lung injury induced by galt gene editing in mouse
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  21. Targeted Therapeutic Genome Engineering: Opportunities and Bottlenecks in Medical Translation
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  22. Research progress on non-viral vectors of CRISPR/Cas9 system
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  23. Application in Gene Editing in Ovarian Cancer Therapy
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  29. Cationic Polymers and Polymeric Micelles as Plasmid DNA and CRISPR-Cas9 Ribonucleoprotein Delivery Vehicles
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  34. Gene Delivery for Cancer Immunotherapy
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  35. CRISPR-Cas9 Fluorine-Containing PEI Nanomedicine Inhibits the Growth of Hepatocellular Carcinoma Cells by Knocking Out NEDD8-E2 Conjugase UBC12 (UBE2M)
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  41. Compositional Optimization of CRISPR/Cas9 Lipid Nanoparticles for Efficient Knockdown of Target Genes
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  44. Nano Delivery Systems for In Vivo CRISPR/Cas-Based Gene Therapy: From Vectors to Clinical Outcomes
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  45. BindingDB Entry 50000152: Fragment-Based Discovery and Optimization of Enzyme Inhibitors by Docking of Commercial Chemical Space.
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