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3
Glycosylated carriers for cell-selective and nuclear delivery of nucleic acids.
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Non-viral Delivery Systems for Breast Cancer Gene Therapy.
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Nonviral Nanoparticles for CRISPR-Based Genome Editing: Is It Just a Simple Adaption of What Have Been Developed for Nucleic Acid Delivery?
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Gene Delivery Particle Engineering Strategies for Shape-dependent Targeting of Cells and Tissues.
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Non-viral nucleic acid containing nanoparticles as cancer therapeutics.
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本文引用的文献

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Restoration of tumour-growth suppression in vivo via systemic nanoparticle-mediated delivery of PTEN mRNA.
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Reducible Branched Ester-Amine Quadpolymers (rBEAQs) Codelivering Plasmid DNA and RNA Oligonucleotides Enable CRISPR/Cas9 Genome Editing.
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Inhaled Nanoformulated mRNA Polyplexes for Protein Production in Lung Epithelium.
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Multifunctional Vector for Delivery of Genome Editing Plasmid Targeting β-Catenin to Remodulate Cancer Cell Properties.
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Non-Viral Delivery To Enable Genome Editing.
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High-throughput in vivo screen of functional mRNA delivery identifies nanoparticles for endothelial cell gene editing.
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Synthesis and Characterization of Quaternized Poly(β-amino ester) for Highly Efficient Delivery of Small Interfering RNA.
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Lipid Nanoparticle Formulations for Enhanced Co-delivery of siRNA and mRNA.
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Lipid-Based Liquid Crystalline Nanoparticles Facilitate Cytosolic Delivery of siRNA via Structural Transformation.
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