SiRNA Delivery Methods : Methods and Protocols /
| Autor Corporativo: | |
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| Otros Autores: | , |
| Formato: | eBook |
| Lenguaje: | English |
| Publicado: |
New York, NY :
Springer New York : Imprint: Humana,
2016.
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| Edición: | 1st ed. 2016. |
| Colección: | Methods in Molecular Biology,
1364 |
| Materias: |
Tabla de Contenidos:
- Synthesis and Conjugation of Small Interfering RiboNucleic Neutral siRNNs.- Liver-Targeted siRNA Delivery Using Biodegradable Poly(amide) Polymer Conjugates.- PepFect6 Mediated siRNA Delivery into Organotypic Cultures.- Highly Efficient siRNA Delivery Mediated by Cationic Helical Polypeptides and Polypeptide-Based Nanosystems.- Disulfide-Bridged Cleavable PEGylation of Poly-L-Lysine for siRNA Delivery.- Preparation of a Cyclic RGD: Modified Liposomal siRNA Formulation for Use in Active Targeting to Tumor and Tumor Endothelial Cells
- A Multifunctional Envelope-Type Nano Device Containing A pH-Sensitive Cationic Lipid for Efficient Delivery of Short Interfering RNA to Hepatocytes In Vivo
- Bioreducible Poly(Beta-Amino Ester)s for Intracellular Delivery of siRNA.- Preparation of Polyion Complex Micelles Using Block Copolymers for siRNA Delivery.- Delivery of Small Interfering RNAs to Cells via Exosomes
- Dendrimer Nanovectors for siRNA Delivery.- Chitosan Nanoparticles for siRNA Delivery In Vitro
- Non-Covalently Functionalized of Single-Walled Carbon Nanotubes by DSPE-PEG-PEI for siRNA Delivery.- siRNA In Vivo Targeted Delivery to Murine Dendritic Cells by Oral Administration of Recombinant Yeast.- TLR9 Targeted siRNA Delivery In Vivo
- Aptamer-miRNA Conjugates for Cancer Cells Targeted Delivery
- Method for Confirming Cytoplasmic Delivery of RNA Aptamers
- Hapten-Binding Bispecific Antibodies for Targeted Delivery of siRNA and siRNA-Containing Nanoparticles.- Stable Delivery of CCR5 Directed shRNA into Human Primary Peripheral Blood Mononuclear Cells and Hematopoietic Stem/Progenitor Cells via a Lentiviral Vector
- Hepatic Delivery of Artificial Micro RNAs Using Helper-Dependent Adenoviral Vectors.- Intravascular AAV9 Administration for Delivering RNA Silencing Constructs to the CNS and Periphery.- Efficient Gene Suppression in Dorsal Root Ganglia (DRG) and Spinal Cord Using Adeno-Associated Virus (AAV) Vector Encoding Short-Hairpin RNA.- Synthetic siRNA Delivery: Progress and Prospects.