Targeted adenovirus gene transfer to endothelial and smooth muscle cells by using bispecific antibodies
about
Structural and phylogenetic analysis of adenovirus hexons by use of high-resolution x-ray crystallographic, molecular modeling, and sequence-based methodsDevelopment of a generic adenovirus delivery system based on structure-guided design of bispecific trimeric DARPin adaptersRecombinant human adenovirus: targeting to the human transferrin receptor improves gene transfer to brain microcapillary endotheliumGeneral strategy for broadening adenovirus tropism.Recent advances in genetic modification of adenovirus vectors for cancer treatmentHer2-specific multivalent adapters confer designed tropism to adenovirus for gene targetingEfficient gene transfer into human CD34(+) cells by a retargeted adenovirus vectorEctodomain of coxsackievirus and adenovirus receptor genetically fused to epidermal growth factor mediates adenovirus targeting to epidermal growth factor receptor-positive cells.Fiber swap between adenovirus subgroups B and C alters intracellular trafficking of adenovirus gene transfer vectors.Mutations in the DG loop of adenovirus type 5 fiber knob protein abolish high-affinity binding to its cellular receptor CAR.Reduction in TRPC4 expression specifically attenuates G-protein coupled receptor-stimulated increases in intracellular calcium in human myometrial cells.Enhancement of adenovirus vector entry into CD70-positive B-cell Lines by using a bispecific CD70-adenovirus fiber antibodyAdenovirus type 5 viral particles pseudotyped with mutagenized fiber proteins show diminished infectivity of coxsackie B-adenovirus receptor-bearing cells.Targeting the urokinase plasminogen activator receptor enhances gene transfer to human airway epithelia.Retargeting of adenovirus vectors through genetic fusion of a single-chain or single-domain antibody to capsid protein IX.Adenoviral targeting using genetically incorporated camelid single variable domains.Artificial extension of the adenovirus fiber shaft inhibits infectivity in coxsackievirus and adenovirus receptor-positive cell lines.Engineering of adenovirus vectors containing heterologous peptide sequences in the C terminus of capsid protein IX.Avidin-based targeting and purification of a protein IX-modified, metabolically biotinylated adenoviral vector.Gene therapy for cerebral vascular disease: update 2003.Redirected infection of directly biotinylated recombinant adenovirus vectors through cell surface receptors and antigens.Targeted adenovirus-mediated gene delivery to T cells via CD3.Structural and functional determinants in adenovirus type 2 penton base recombinant protein.Metabolic biotinylation of recombinant proteins in mammalian cells and in mice.Identification of HI-like loop in CELO adenovirus fiber for incorporation of receptor binding motifs.Current advances and future challenges in Adenoviral vector biology and targetingIncorporation of adenovirus in calcium phosphate precipitates enhances gene transfer to airway epithelia in vitro and in vivo.Strategies to overcome host immunity to adenovirus vectors in vaccine development.Viral vectors for vascular gene therapyHelper-Dependent Adenoviral Vectors.Retargeting of viruses to generate oncolytic agents.Antibody-mediated targeted gene transfer of helper virus-free HSV-1 vectors to rat neocortical neurons that contain either NMDA receptor 2B or 2A subunits.Tropism-modification strategies for targeted gene delivery using adenoviral vectors.Fiberless recombinant adenoviruses: virus maturation and infectivity in the absence of fiber.Group D adenoviruses infect primary central nervous system cells more efficiently than those from group C.Coxsackievirus and adenovirus receptor cytoplasmic and transmembrane domains are not essential for coxsackievirus and adenovirus infection.Characterization of an adenovirus vector containing a heterologous peptide epitope in the HI loop of the fiber knob.Dependence of adenovirus infectivity on length of the fiber shaft domain.Retargeting the coxsackievirus and adenovirus receptor to the apical surface of polarized epithelial cells reveals the glycocalyx as a barrier to adenovirus-mediated gene transfer.Construction of a pseudoreceptor that mediates transduction by adenoviruses expressing a ligand in fiber or penton base.
P2860
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P2860
Targeted adenovirus gene transfer to endothelial and smooth muscle cells by using bispecific antibodies
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
Targeted adenovirus gene trans ...... by using bispecific antibodies
@ast
Targeted adenovirus gene trans ...... by using bispecific antibodies
@en
type
label
Targeted adenovirus gene trans ...... by using bispecific antibodies
@ast
Targeted adenovirus gene trans ...... by using bispecific antibodies
@en
prefLabel
Targeted adenovirus gene trans ...... by using bispecific antibodies
@ast
Targeted adenovirus gene trans ...... by using bispecific antibodies
@en
P2093
P2860
P921
P1433
P1476
Targeted adenovirus gene trans ...... by using bispecific antibodies
@en
P2093
P2860
P304
P407
P50
P577
1996-10-01T00:00:00Z