Lentiviral vectors for enhanced gene expression in human hematopoietic cells.
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Erythroid-specific human factor IX delivery from in vivo selected hematopoietic stem cells following nonmyeloablative conditioning in hemophilia B miceImpact of age at administration, lysosomal storage, and transgene regulatory elements on AAV2/8-mediated rat liver transductionA Hepadnavirus Regulatory Element Enhances Expression of a Type 2 Bovine Viral Diarrhea Virus E2 Protein from a Bovine Herpesvirus 1 VectorNon-integrative lentivirus drives high-frequency cre-mediated cassette exchange in human cellsCurrent progress and challenges in HIV gene therapyWoodchuck post-transcriptional element induces nuclear export of myotonic dystrophy 3' untranslated region transcripts.Correction of murine ADAMTS13 deficiency by hematopoietic progenitor cell-mediated gene therapySynthetic design of strong promotersHemato-endothelial differentiation from lentiviral-transduced human embryonic stem cells retains durable reporter gene expression under the control of ubiquitin promoter.Evaluation of combinatorial cis-regulatory elements for stable gene expression in chicken cells.Peripherally expressed neprilysin reduces brain amyloid burden: a novel approach for treating Alzheimer's disease.VIP-expressing dendritic cells protect against spontaneous autoimmune peripheral polyneuropathy.Stable transgene expression in primitive human CD34+ hematopoietic stem/progenitor cells, using the Sleeping Beauty transposon systemEngineering of human pluripotent stem cells by AAV-mediated gene targeting.Rhesus monkey placental transgene expression after lentiviral gene transfer into preimplantation embryos.Design of an HIV-1 lentiviral-based gene-trap vector to detect developmentally regulated genes in mammalian cells.Cytotoxicity associated with artemis overexpression after lentiviral vector-mediated gene transfer.Silencing of gene expression: implications for design of retrovirus vectors.A high-capacity, capsid-modified hybrid adenovirus/adeno-associated virus vector for stable transduction of human hematopoietic cellsBypass of senescence, immortalization, and transformation of human hematopoietic progenitor cells.The murine stem cell virus promoter drives correlated transgene expression in the leukocytes and cerebellar Purkinje cells of transgenic miceInhibition of Grb2 expression demonstrates an important role in BCR-ABL-mediated MAPK activation and transformation of primary human hematopoietic cellsDevelopment of gene therapy for blood disorders by gene transfer into haematopoietic stem cells.Muscle fiber type-predominant promoter activity in lentiviral-mediated transgenic mouse.Inhibition of histone deacetylation in 293GPG packaging cell line improves the production of self-inactivating MLV-derived retroviral vectorsRescue of splicing-mediated intron loss maximizes expression in lentiviral vectors containing the human ubiquitin C promoter.Gene therapy for canine leukocyte adhesion deficiency with lentiviral vectors using the murine stem cell virus and human phosphoglycerate kinase promoters.Vectors for the treatment of autoimmune disease.Optimization of multimodal imaging of mesenchymal stem cells using the human sodium iodide symporter for PET and Cerenkov luminescence imaging.Dual transgene expression in murine cerebellar Purkinje neurons by viral transduction in vivoStrategies to insulate lentiviral vector-expressed transgenesHigh-frequency epigenetic repression and silencing of retroviruses can be antagonized by histone deacetylase inhibitors and transcriptional activators, but uniform reactivation in cell clones is restricted by additional mechanisms.Lentivirus-mediated gene transfer to the respiratory epithelium: a promising approach to gene therapy of cystic fibrosis.Combination of Sleeping Beauty transposition and chemically induced dimerization selection for robust production of engineered cells.Vector design for expression of O6-methylguanine-DNA methyltransferase in hematopoietic cells.Lentiviral vectors incorporating a human elongation factor 1alpha promoter for the treatment of canine leukocyte adhesion deficiency.Transcriptional burst frequency and burst size are equally modulated across the human genome.Stable gammaretroviral vector expression during embryonic stem cell-derived in vitro hematopoietic development.Reducing the genotoxic potential of retroviral vectors.TLX1/HOX11-mediated disruption of primary thymocyte differentiation prior to the CD4+CD8+ double-positive stage.
P2860
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P2860
Lentiviral vectors for enhanced gene expression in human hematopoietic cells.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年学术文章
@wuu
2000年学术文章
@zh-cn
2000年学术文章
@zh-hans
2000年学术文章
@zh-my
2000年学术文章
@zh-sg
2000年學術文章
@yue
2000年學術文章
@zh
2000年學術文章
@zh-hant
name
Lentiviral vectors for enhanced gene expression in human hematopoietic cells.
@en
type
label
Lentiviral vectors for enhanced gene expression in human hematopoietic cells.
@en
prefLabel
Lentiviral vectors for enhanced gene expression in human hematopoietic cells.
@en
P2093
P356
P1433
P1476
Lentiviral vectors for enhanced gene expression in human hematopoietic cells.
@en
P2093
P304
P356
10.1006/MTHE.2000.0190
P577
2000-11-01T00:00:00Z