Development of lentiviral vectors for gene therapy for human diseases.
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Construction and molecular analysis of gene transfer systems derived from bovine immunodeficiency virusCorrection of mucopolysaccharidosis type IIIb fibroblasts by lentiviral vector-mediated gene transferGene Therapy for Pediatric Cancer: State of the Art and Future PerspectivesControlling neuropathic pain by adeno-associated virus driven production of the anti-inflammatory cytokine, interleukin-10Recent advances in live cell imaging of hepatoma cellsTargeting of Magnetic Nanoparticle-coated Microbubbles to the Vascular Wall Empowers Site-specific Lentiviral Gene Delivery in vivoCurrent progress and challenges in HIV gene therapyIncorporating double copies of a chromatin insulator into lentiviral vectors results in less viral integrantsHepatitis B virus inhibition in mice by lentiviral vector mediated short hairpin RNA.R88-APOBEC3Gm Inhibits the Replication of Both Drug-resistant Strains of HIV-1 and Viruses Produced From Latently Infected CellsHIV-1-based defective lentiviral vectors efficiently transduce human monocytes-derived macrophages and suppress replication of wild-type HIV-1Placental gene transfer: transgene screening in mice for trophic effects on the placenta.si-RNA-Mediated Silencing of ADRBK1 Gene Attenuates Breast Cancer Cell Proliferation.RNA 3' readthrough of oncoretrovirus and lentivirus: implications for vector safety and efficacy.Gene therapy for cerebral vascular disease: update 2003.Transplantation of ATP7B-transduced bone marrow mesenchymal stem cells decreases copper overload in rats.Proinflammatory cytokine gene induction by human T-cell leukemia virus type 1 (HTLV-1) and HTLV-2 Tax in primary human glial cells.Heterologous human immunodeficiency virus type 1 lentiviral vectors packaging a simian immunodeficiency virus-derived genome display a specific postentry transduction defect in dendritic cells.General strategy for decoration of enveloped viruses with functionally active lipid-modified cytokines.IL10 released by a new inflammation-regulated lentiviral system efficiently attenuates zymosan-induced arthritisSuppression of EZH2 Prevents the Shift of Osteoporotic MSC Fate to Adipocyte and Enhances Bone Formation During OsteoporosisHuman T-cell leukemia virus type 1 tax oncoprotein suppression of multilineage hematopoiesis of CD34+ cells in vitroInterfering RNA-mediated purine analog resistance for in vitro and in vivo cell selection.Polysaccharide-modified scaffolds for controlled lentivirus delivery in vitro and after spinal cord injuryA method for detecting and preventing negative RNA interference in preparation of lentiviral vectors for siRNA delivery.Human T-cell leukemia virus type 1 (HTLV-1) and HTLV-2 tax oncoproteins modulate cell cycle progression and apoptosis.MicroRNA-93-5p may participate in the formation of morphine tolerance in bone cancer pain mouse model by targeting Smad5.Glioblastoma multiforme: State of the art and future therapeutics.Pseudotyping of lentiviral vector with novel vesiculovirus envelope glycoproteins derived from Chandipura and Piry viruses.Locus control region of the human CD2 gene in a lentivirus vector confers position-independent transgene expression.Pseudotyped adeno-associated viral vector tropism and transduction efficiencies in murine wound healingMaximization of loading and stability of ssDNA:iron oxide nanoparticle complexes formed through electrostatic interaction.Transgene expression in various organs post BM-HSC transplantation.Comparison of transduction efficiency among various lentiviruses containing GFP reporter in bone marrow hematopoietic stem cell transplantation.Pseudotyped adeno-associated viral vectors for gene transfer in dermal fibroblasts: implications for wound-healing applications.Lentivirus-mediated LIGHT overexpression inhibits human colorectal carcinoma cell growth in vitro and in vivo.CRISPR/Cas9 Genome-Editing System in Human Stem Cells: Current Status and Future Prospects.DMSO increases efficiency of genome editing at two non-coding loci.
P2860
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P2860
Development of lentiviral vectors for gene therapy for human diseases.
description
2000 nî lūn-bûn
@nan
2000 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Development of lentiviral vectors for gene therapy for human diseases.
@ast
Development of lentiviral vectors for gene therapy for human diseases.
@en
type
label
Development of lentiviral vectors for gene therapy for human diseases.
@ast
Development of lentiviral vectors for gene therapy for human diseases.
@en
prefLabel
Development of lentiviral vectors for gene therapy for human diseases.
@ast
Development of lentiviral vectors for gene therapy for human diseases.
@en
P1433
P1476
Development of lentiviral vectors for gene therapy for human diseases
@en
P2093
Buchschacher GL Jr
Wong-Staal F
P304
P407
P577
2000-04-01T00:00:00Z