Efficient gene transfer into nondividing cells by adeno-associated virus-based vectors.
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Persistent expression of human clotting factor IX from mouse liver after intravenous injection of adeno-associated virus vectorsAdeno-associated Virus as a Mammalian DNA VectorMicroutrophin delivery through rAAV6 increases lifespan and improves muscle function in dystrophic dystrophin/utrophin-deficient miceTransduction of dendritic cells by DNA viral vectors directs the immune response to transgene products in muscle fibers.Recombinant human parvovirus B19 vectors: erythroid cell-specific delivery and expression of transduced genesCharacterization of wild-type adeno-associated virus type 2-like particles generated during recombinant viral vector production and strategies for their eliminationAdeno-associated virus-mediated transfer of endothelial nitric oxide synthase gene reduces the vasoconstrictive response.Recombinant AAV2 transduction of primitive human hematopoietic stem cells capable of serial engraftment in immune-deficient mice.DNA synthesis and topoisomerase inhibitors increase transduction by adeno-associated virus vectorsTherapeutic approaches to muscular dystrophy.Intracellular transport of recombinant adeno-associated virus vectors.Recombinant adeno-associated virus-mediated high-efficiency, transient expression of the murine cationic amino acid transporter (ecotropic retroviral receptor) permits stable transduction of human HeLa cells by ecotropic retroviral vectors.Efficient long-term gene transfer into muscle tissue of immunocompetent mice by adeno-associated virus vector.Analysis of recombinant adeno-associated virus packaging and requirements for rep and cap gene products.The Rep78 gene product of adeno-associated virus (AAV) self-associates to form a hexameric complex in the presence of AAV ori sequences.Cloning of adeno-associated virus type 4 (AAV4) and generation of recombinant AAV4 particles.Gene delivery to skeletal muscle results in sustained expression and systemic delivery of a therapeutic proteinThree-dimensional multipotent progenitor cell aggregates for expansion, osteogenic differentiation and 'in vivo' tracing with AAV vector serotype 6.AAV capsid CD8+ T-cell epitopes are highly conserved across AAV serotypesLysine: Is it worth more?Use of Adeno-Associated and Herpes Simplex Viral Vectors for In Vivo Neuronal Expression in Mice.Tissue specific promoters improve specificity of AAV9 mediated transgene expression following intra-vascular gene delivery in neonatal mice.Protective CD8+ T-cell responses to cytomegalovirus driven by rAAV/GFP/IE1 loading of dendritic cellsEmerging strategies for cell and gene therapy of the muscular dystrophiesAdeno-associated virus-2 and its primary cellular receptor--Cryo-EM structure of a heparin complex.Site-specific integration by adeno-associated virusLarge animal models of neurological disorders for gene therapy.Systemic gene delivery transduces the enteric nervous system of guinea pigs and cynomolgus macaques.AAV-ID: A Rapid and Robust Assay for Batch-to-Batch Consistency Evaluation of AAV Preparations.Recombinant adeno-associated virus mediates a high level of gene transfer but less efficient integration in the K562 human hematopoietic cell lineRole for highly regulated rep gene expression in adeno-associated virus vector production.Efficient production of adeno-associated virus vectors using split-type helper plasmids.Successful transfection of genes using AAV-2/9 vector in swine coronary and peripheral arteries.Enhanced long-term transduction and multilineage engraftment of human hematopoietic stem cells transduced with tyrosine-modified recombinant adeno-associated virus serotype 2.Stem cell technology. Interview by Abi BergerAdeno-associated virus vector containing the herpes simplex virus thymidine kinase gene causes complete regression of intracerebrally implanted human gliomas in mice, in conjunction with ganciclovir administration.
P2860
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P2860
Efficient gene transfer into nondividing cells by adeno-associated virus-based vectors.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Efficient gene transfer into nondividing cells by adeno-associated virus-based vectors.
@ast
Efficient gene transfer into nondividing cells by adeno-associated virus-based vectors.
@en
type
label
Efficient gene transfer into nondividing cells by adeno-associated virus-based vectors.
@ast
Efficient gene transfer into nondividing cells by adeno-associated virus-based vectors.
@en
prefLabel
Efficient gene transfer into nondividing cells by adeno-associated virus-based vectors.
@ast
Efficient gene transfer into nondividing cells by adeno-associated virus-based vectors.
@en
P2093
P2860
P1433
P1476
Efficient gene transfer into nondividing cells by adeno-associated virus-based vectors
@en
P2093
G Podsakoff
S Chatterjee
P2860
P304
P407
P577
1994-09-01T00:00:00Z