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Titlebook: SiRNA Delivery Methods; Methods and Protocol Kato Shum,John Rossi Book 2016 Springer Science+Business Media New York 2016 RNA interference.

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Preparation of Polyion Complex Micelles Using Block Copolymers for SiRNA Delivery,tability assay for SiRNA-loaded PIC micelles in the presence of serum using fluorescence correlation spectroscopy and a luciferase assay for cultured cancer cells stably expressing luciferase, thus providing the biological criteria for further medicinal applications.
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Non-Covalently Functionalized of Single-Walled Carbon Nanotubes by DSPE-PEG-PEI for SiRNA Delivery,istearoyl-sn-glycero-3-phosphoethanolamine-.-[amino(polyethylene glycol)-2000] (DSPE-PEG) was generated and the products used to disperse CNT to form DSPE-PEG-PEI/CNT (DGI/C), an agent capable of facilitating SiRNA delivery to cells in vitro and organs and cells in vivo.
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SiRNA In Vivo-Targeted Delivery to Murine Dendritic Cells by Oral Administration of Recombinant Yea of recombinant yeast (.). Here, we describe the details of the promising and innovative approach based on oral administration of recombinant yeast that allows in vivo-targeted delivery of functional SiRNA to murine intestinal DCs.
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Disulfide-Bridged Cleavable PEGylation of Poly-,-Lysine for SiRNA Delivery,ncluding ring-opening polymerization (ROP) of ε-benzyloxycarbonyl-.-lysine .-carboxyanhydride (zLL-NCA) monomers to yield PEG-cleavable polylysine, examination on bio-stability and bio-efficacy of its gene complexes are described.
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Synthesis and Conjugation of Small Interfering Ribonucleic Neutral SiRNNs, the phosphate backbone negative charge by synthesis with bioreversible phosphotriester groups that are enzymatically cleaved off in the cytoplasm of cells. Here we describe the synthesis and purification of siRNN conjugates that induce in vivo target gene knockdown following systemic delivery into mice.
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TLR9-Targeted SiRNA Delivery In Vivo,sitive cells in the absence of transfection reagents, inducing target gene silencing. The CpG-SiRNA strategy allows for effective targeting of TLR9-positive cells in vivo after local or systemic administration of these oligonucleotides into mice.
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