about
A capsid-modified helper-dependent adenovirus vector containing the beta-globin locus control region displays a nonrandom integration pattern and allows stable, erythroid-specific gene expression.Gene therapy in clinical medicineIn vivo electroporation mediated gene delivery to the beating heart.Targeted chromosomal insertion of large DNA into the human genome by a fiber-modified high-capacity adenovirus-based vector system.Combinatorial anti-HIV gene therapy: using a multipronged approach to reach beyond HAARTHybrid adeno-associated viral vectors utilizing transposase-mediated somatic integration for stable transgene expression in human cells.Protection of mice from lethal Escherichia coli infection by chimeric human bactericidal/permeability-increasing protein and immunoglobulin G1 Fc gene deliveryVersatility of gene therapy vectors through viruses.Helper-dependent adenoviral vectors in experimental gene therapy.Gene therapy of fibroproliferative vasculopathies: current ideas in molecular mechanisms and biomedical technology.Nerve conduits and growth factor delivery in peripheral nerve repair.siRNA Genome Screening Approaches to Therapeutic Drug Repositioning.Gene therapy: a potential approach for cancer pain.BTK gene targeting by homologous recombination using a helper-dependent adenovirus/adeno-associated virus hybrid vector.Derivation and characterization of a transgene-free human induced pluripotent stem cell line and conversion into defined clinical-grade conditions.Clinical potentials of human pluripotent stem cells.Homologous recombination is required for AAV-mediated gene targeting.Replication-competent adenovirus formation in 293 cells: the recombination-based rate is influenced by structure and location of the transgene cassette and not increased by overproduction of HsRad51, Rad51-interacting, or E2F family proteins.RNA-Generated and Gene-Edited Induced Pluripotent Stem Cells for Disease Modeling and Therapy.Foamy virus--adenovirus hybrid vectors.Mitochondrial imaging in dorsal root ganglion neurons following the application of inducible adenoviral vector expressing two fluorescent proteins.Genomic integration of adenoviral gene transfer vectors following transduction of fertilized mouse oocytes.Probing GATA factor function in mouse Leydig cells via testicular injection of adenoviral vectors.
P2860
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P2860
description
2002 nî lūn-bûn
@nan
2002 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Adenovirus as an integrating vector.
@ast
Adenovirus as an integrating vector.
@en
Adenovirus as an integrating vector.
@nl
type
label
Adenovirus as an integrating vector.
@ast
Adenovirus as an integrating vector.
@en
Adenovirus as an integrating vector.
@nl
prefLabel
Adenovirus as an integrating vector.
@ast
Adenovirus as an integrating vector.
@en
Adenovirus as an integrating vector.
@nl
P356
P1433
P1476
Adenovirus as an integrating vector.
@en
P304
P356
10.2174/1566523024605591
P407
P577
2002-05-01T00:00:00Z