GRAZE
发表于 2025-3-28 14:48:20
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.
maintenance
发表于 2025-3-28 22:34:04
Non-Covalently Functionalized of Single-Walled Carbon Nanotubes by DSPE-PEG-PEI for SiRNA Delivery,istearoyl-sn-glycero-3-phosphoethanolamine-.- (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.
pester
发表于 2025-3-28 23:42:27
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.
阻挡
发表于 2025-3-29 05:14:11
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招惹
发表于 2025-3-29 09:52:58
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.
因无茶而冷淡
发表于 2025-3-29 11:47:01
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disparage
发表于 2025-3-29 15:39:08
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.
卧虎藏龙
发表于 2025-3-29 20:03:40
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四溢
发表于 2025-3-30 02:46:12
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intellect
发表于 2025-3-30 06:48:48
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.