Targeted gene transfer into hepatoma cells with lipopolyamine-condensed DNA particles presenting galactose ligands: a stage toward artificial viruses.
about
Gene delivery: a single nuclear localization signal peptide is sufficient to carry DNA to the cell nucleusA versatile vector for gene and oligonucleotide transfer into cells in culture and in vivo: polyethylenimineDynamics of transient pores in stretched vesicles.Polyamine structural effects on the induction and stabilization of liquid crystalline DNA: potential applications to DNA packaging, gene therapy and polyamine therapeutics.Sugar-based tertiary amino gemini surfactants with a vesicle-to-micelle transition in the endosomal pH range mediate efficient transfection in vitro.Strategy of liver-directed gene therapy: present status and future prospects.The potential of nucleic acid repair in functional genomics.Hepatocytes targeting of cationic liposomes modified with soybean sterylglucoside and polyethylene glycolMonomolecular collapse of plasmid DNA into stable virus-like particles.Genetic modification of hematopoietic stem cells with nonviral systems: past progress and future prospects.Fusigenic viral liposome for gene therapy in cardiovascular diseases.Expression of scFv-Mel-Gal4 triple fusion protein as a targeted DNA-carrier in Escherichia Coli.Comparative affinity of synthetic multi-antennary galactosyl derivatives for the Gal/GalNAc receptor of rat hepatocytes and peritoneal macrophages.Polyethyleneimine grafted with pluronic P85 enhances Ku86 antisense delivery and the ionizing radiation treatment efficacy in vivo.Targeted antisense modulation of inflammatory cytokine receptors.On the interpretation of Raman spectra of 1-aminooxy-spermine/DNA complexes.Target cell-specific DNA transfer mediated by a chimeric multidomain protein. Novel non-viral gene delivery system.Spherulites: onion-like vesicles as nanomedicines.Mannosylated chitosan nanoparticles for delivery of antisense oligonucleotides for macrophage targeting.Biotinylated photocleavable polyethylenimine: capture and triggered release of nucleic acids from solid supports.M-PEIs nanogels: potential nonviral vector for systemic plasmid delivery to tumor cells.A physicochemical approach for predicting the effectiveness of peptide-based gene delivery systems for use in plasmid-based gene therapy.Supramolecular Virus-Like Nanorods by Coassembly of a Triblock Polypeptide and Reversible Coordination Polymers.The nuclear pore complex is involved in nuclear transfer of plasmid DNA condensed with an oligolysine-RGD peptide containing nuclear localisation properties.Liver-targeted gene transfer into a human hepatoblastoma cell line and in vivo by sterylglucoside-containing cationic liposomes.Receptor-mediated gene delivery to HepG2 cells by ternary assemblies containing cationic liposomes and cationized asialoorosomucoid.Diseases originate and terminate by genes: unraveling nonviral gene delivery.Folate-targeted, anionic liposome-entrapped polylysine-condensed DNA for tumor cell-specific gene transfer.Binding of cationic alpha-helical peptides to plasmid DNA and their gene transfer abilities into cells.DNA/polyethylenimine transfection particles: influence of ligands, polymer size, and PEGylation on internalization and gene expression.Design and self-assembly of simple coat proteins for artificial viruses.Optimization of cell surface binding enhances efficiency and specificity of molecular conjugate gene delivery.Characteristics and biodistribution of soybean sterylglucoside and polyethylene glycol-modified cationic liposomes and their complexes with antisense oligodeoxynucleotide.Comparing different sterol containing solid lipid nanoparticles for targeted delivery of quercetin in hepatocellular carcinoma.Interactions of heparin with human skin cells: binding, location, and transdermal penetration.Gene transfer mediated by fusion protein hemagglutinin reconstituted in cationic lipid vesicles.An integrin-targeted non-viral vector for pulmonary gene therapy.Tumour gene expression from C12 spermine amphiphile gene delivery systems.Receptor ligand-facilitated cationic liposome delivery of anti-HIV-1 Rev-binding aptamer and ribozyme DNAs.DNA complexes with block and graft copolymers of N-(2-hydroxypropyl)methacrylamide and 2-(trimethylammonio)ethyl methacrylate.
P2860
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P2860
Targeted gene transfer into hepatoma cells with lipopolyamine-condensed DNA particles presenting galactose ligands: a stage toward artificial viruses.
description
1995 nî lūn-bûn
@nan
1995 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Targeted gene transfer into he ...... age toward artificial viruses.
@ast
Targeted gene transfer into he ...... age toward artificial viruses.
@en
Targeted gene transfer into he ...... age toward artificial viruses.
@nl
type
label
Targeted gene transfer into he ...... age toward artificial viruses.
@ast
Targeted gene transfer into he ...... age toward artificial viruses.
@en
Targeted gene transfer into he ...... age toward artificial viruses.
@nl
prefLabel
Targeted gene transfer into he ...... age toward artificial viruses.
@ast
Targeted gene transfer into he ...... age toward artificial viruses.
@en
Targeted gene transfer into he ...... age toward artificial viruses.
@nl
P2093
P2860
P356
P1476
Targeted gene transfer into he ...... age toward artificial viruses.
@en
P2093
P2860
P304
P356
10.1073/PNAS.92.5.1744
P407
P577
1995-02-01T00:00:00Z