Critical factors influencing stable transduction of human CD34(+) cells with HIV-1-derived lentiviral vectors.
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Ethanol as a prodrug: brain metabolism of ethanol mediates its reinforcing effectsDifferences in tropism and pH dependence for glycoproteins from the Clade B1 arenaviruses: Implications for receptor usage and pathogenicityQuantitative comparison of constitutive promoters in human ES cellsTransduction of human primitive repopulating hematopoietic cells with lentiviral vectors pseudotyped with various envelope proteins.Axonal degeneration is blocked by nicotinamide mononucleotide adenylyltransferase (Nmnat) protein transduction into transected axons.Retrograde monosynaptic tracing reveals the temporal evolution of inputs onto new neurons in the adult dentate gyrus and olfactory bulb.Evidence that stable retroviral transduction and cell survival following DNA integration depend on components of the nonhomologous end joining repair pathway.HIV-1-based defective lentiviral vectors efficiently transduce human monocytes-derived macrophages and suppress replication of wild-type HIV-1Entry kinetics and cell-cell transmission of surface-bound retroviral vector particles.Mobilization and mechanism of transcription of integrated self-inactivating lentiviral vectors.Engineering the human thymic microenvironment to support thymopoiesis in vivo.Enhanced genetic modification of adult growth factor mobilized peripheral blood hematopoietic stem and progenitor cells with rapamycin.Transmembrane protein aptamers that inhibit CCR5 expression and HIV coreceptor functionIn vivo biosafety model to assess the risk of adverse events from retroviral and lentiviral vectors.The HIV-1 Rev protein enhances encapsidation of unspliced and spliced, RRE-containing lentiviral vector RNAHighly efficient large-scale lentiviral vector concentration by tandem tangential flow filtration.Cell-cell transmission of VSV-G pseudotyped lentivector particles.Ex vivo γ-retroviral gene therapy of dogs with X-linked severe combined immunodeficiency and the development of a thymic T cell lymphoma.Quantification of lentiviral vector copy numbers in individual hematopoietic colony-forming cells shows vector dose-dependent effects on the frequency and level of transduction.Human immunodeficiency virus type 1-derived lentivirus vectors pseudotyped with envelope glycoproteins derived from Ross River virus and Semliki Forest virusEffects of vector backbone and pseudotype on lentiviral vector-mediated gene transfer: studies in infant ADA-deficient mice and rhesus monkeys.The Moloney murine leukemia virus repressor binding site represses expression in murine and human hematopoietic stem cellsHematopoietic stem cell gene therapy with drug resistance genes: an update.Expansion of multipotent and lymphoid-committed human progenitors through intracellular dimerization of Mpl.Integrated self-inactivating lentiviral vectors produce full-length genomic transcripts competent for encapsidation and integrationVectofusin-1, a new viral entry enhancer, strongly promotes lentiviral transduction of human hematopoietic stem cells.Cell cycle requirements for transduction by foamy virus vectors compared to those of oncovirus and lentivirus vectors.Simian immunodeficiency virus lentivector corrects human X-linked chronic granulomatous disease in the NOD/SCID mouse xenograft.Cellular microvesicle pathways can be targeted to transfer genetic information between non-immune cells.Mesenchymal stem cells for the sustained in vivo delivery of bioactive factors.CD4+CD25- T cells transduced to express MHC class I-restricted epitope-specific TCR synthesize Th1 cytokines and exhibit MHC class I-restricted cytolytic effector function in a human melanoma model.Lentivirus-mediated bifunctional cell labeling for in vivo melanoma studyEnrichment of human hematopoietic stem/progenitor cells facilitates transduction for stem cell gene therapy.Semi-automated closed system manufacturing of lentivirus gene-modified haematopoietic stem cells for gene therapyIntegration-deficient lentiviral vectors: a slow coming of age.Fast and efficient multitransgenic modification of human pluripotent stem cells.Lessons from genetically altered mesenchymal stem cells (MSCs): candidates for improved MSC-directed myocardial repair.Development of gene therapy for thalassemia.Lentivirus transduction of human osteoclast precursor cells and differentiation into functional osteoclastsTissue-specific restriction of cyclophilin A-independent HIV-1- and SIV-derived lentiviral vectors.
P2860
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P2860
Critical factors influencing stable transduction of human CD34(+) cells with HIV-1-derived lentiviral vectors.
description
2000 nî lūn-bûn
@nan
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
2000年论文
@zh
2000年论文
@zh-cn
name
Critical factors influencing s ...... -1-derived lentiviral vectors.
@en
type
label
Critical factors influencing s ...... -1-derived lentiviral vectors.
@en
prefLabel
Critical factors influencing s ...... -1-derived lentiviral vectors.
@en
P2093
P356
P1433
P1476
Critical factors influencing s ...... -1-derived lentiviral vectors.
@en
P2093
P356
10.1006/MTHE.2000.0094
P577
2000-07-01T00:00:00Z