High-efficiency receptor-mediated delivery of small and large (48 kilobase gene constructs using the endosome-disruption activity of defective or chemically inactivated adenovirus particles.
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Analysis of human cytomegalovirus oriLyt sequence requirements in the context of the viral genome.Gene therapy for cystic fibrosis.A recombinant bcl-x s adenovirus selectively induces apoptosis in cancer cells but not in normal bone marrow cells.Progress in cancer gene therapy.Gene transfer into hepatoma cell lines via the serpin enzyme complex receptorCellular uptake and infection by canine parvovirus involves rapid dynamin-regulated clathrin-mediated endocytosis, followed by slower intracellular traffickingReceptor-mediated targeting of gene delivery vectors: insights from molecular mechanisms for improved vehicle design.Bone marrow extracellular matrix molecules improve gene transfer into human hematopoietic cells via retroviral vectors.Gene transfer into the airway epithelium of animals by targeting the polymeric immunoglobulin receptorPriming of tumor-specific T cells in the draining lymph nodes after immunization with interleukin 2-secreting tumor cells: three consecutive stages may be required for successful tumor vaccination.Plasmid DNA entry into postmitotic nuclei of primary rat myotubesExtrachromosomal recombination occurs efficiently in cells defective in various DNA repair systemsTransient gene expression from yeast artificial chromosome DNA in mammalian cells is enhanced by adenovirus.Targeted gene transfer into hepatoma cells with lipopolyamine-condensed DNA particles presenting galactose ligands: a stage toward artificial viruses.Improved biological activity of antisense oligonucleotides conjugated to a fusogenic peptide.AdenovirusUtilization of modified surfactant-associated protein B for delivery of DNA to airway cells in culture.In vivo production of human factor VII in mice after intrasplenic implantation of primary fibroblasts transfected by receptor-mediated, adenovirus-augmented gene delivery.Hybrid proteins between Pseudomonas aeruginosa exotoxin A and poliovirus 2Apro cleave p220 in HeLa cells.Self-assembled mPEG-PCL-g-PEI micelles for simultaneous codelivery of chemotherapeutic drugs and DNA: synthesis and characterization in vitro.Uniqueness, advantages, challenges, solutions, and perspectives in therapeutics applying RNA nanotechnology.A single design strategy for dual sensitive pH probe with a suitable range to map pH in living cells.Distinct effects of endosomal escape and inhibition of endosomal trafficking on gene delivery via electrotransfection.Calcium phosphate nanoparticles: second-generation nonviral vectors in gene therapy.Controlled inactivation of recombinant viruses with vitamin B2.Mechanism of enhancement of DNA expression consequent to cointernalization of a replication-deficient adenovirus and unmodified plasmid DNAAdenovirus inhibition of cell translation facilitates release of virus particles and enhances degradation of the cytokeratin network.Mutations that alter an Arg-Gly-Asp (RGD) sequence in the adenovirus type 2 penton base protein abolish its cell-rounding activity and delay virus reproduction in flat cellsVectors for airway gene delivery.Coupling of adenovirus to transferrin-polylysine/DNA complexes greatly enhances receptor-mediated gene delivery and expression of transfected genesInfluenza virus hemagglutinin HA-2 N-terminal fusogenic peptides augment gene transfer by transferrin-polylysine-DNA complexes: toward a synthetic virus-like gene-transfer vehicleOral tolerization to adenoviral antigens permits long-term gene expression using recombinant adenoviral vectors.Exploiting features of adenovirus replication to support mammalian kinase productionAnalysis of essential viral gene functions after highly efficient adenofection of cells with cloned human cytomegalovirus genomes.Silk-based delivery systems of bioactive molecules.Bacteriophages as vehicles for gene delivery into mammalian cells: prospects and problems.Target cell-specific DNA transfer mediated by a chimeric multidomain protein. Novel non-viral gene delivery system.Drug-conjugated polymers as gene carriers for synergistic therapeutic effect.History of Polymeric Gene Delivery Systems.An FRET-based ratiometric chemosensor for in vitro cellular fluorescence analyses of pH.
P2860
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P2860
High-efficiency receptor-mediated delivery of small and large (48 kilobase gene constructs using the endosome-disruption activity of defective or chemically inactivated adenovirus particles.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on July 1992
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
High-efficiency receptor-media ...... ctivated adenovirus particles.
@en
High-efficiency receptor-mediated delivery of small and large
@nl
type
label
High-efficiency receptor-media ...... ctivated adenovirus particles.
@en
High-efficiency receptor-mediated delivery of small and large
@nl
prefLabel
High-efficiency receptor-media ...... ctivated adenovirus particles.
@en
High-efficiency receptor-mediated delivery of small and large
@nl
P2093
P2860
P356
P1476
High-efficiency receptor-media ...... activated adenovirus particles
@en
P2093
D T Curiel
K Zatloukal
M L Birnstiel
S Phillips
P2860
P304
P356
10.1073/PNAS.89.13.6094
P407
P577
1992-07-01T00:00:00Z