Mutagenesis and oncogenesis by chromosomal insertion of gene transfer vectors.
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In Vivo Delivery Systems for Therapeutic Genome EditingRecent advances of biomaterials in biotherapyGenome-editing Technologies for Gene and Cell TherapyStem cell-based regenerative opportunities for the liver: State of the art and beyondsiRNA Versus miRNA as Therapeutics for Gene SilencingCARs in chronic lymphocytic leukemia -- ready to driveMultiparameter evaluation of in vivo gene delivery using ultrasound-guided, microbubble-enhanced sonoporationSpatial and Temporal Control of Cavitation Allows High In Vitro Transfection Efficiency in the Absence of Transfection Reagents or Contrast AgentsEfficient non-viral ocular gene transfer with compacted DNA nanoparticles.Integration site selection by retroviral vectors: molecular mechanism and clinical consequences.Transcription factor binding sites are genetic determinants of retroviral integration in the human genome.A novel hybrid adenoretroviral vector with more extensive E3 deletion extends transgene expression in submandibular glands.Modified lentiviral LTRs allow Flp recombinase-mediated cassette exchange and in vivo tracing of "factor-free" induced pluripotent stem cells.Stimuli-Responsive Mesoporous Silica NPs as Non-viral Dual siRNA/Chemotherapy Carriers for Triple Negative Breast Cancer.Multifunctional Nucleus-targeting Nanoparticles with Ultra-high Gene Transfection Efficiency for In Vivo Gene TherapymRNA vaccine delivery using lipid nanoparticles.Stem cell marking with promotor-deprived self-inactivating retroviral vectors does not lead to induced clonal imbalance.TAT-mediated transduction of MafA protein in utero results in enhanced pancreatic insulin expression and changes in islet morphologyRepetitive busulfan administration after hematopoietic stem cell gene therapy associated with a dominant HDAC7 clone in a nonhuman primate.siRNA nanoparticle functionalization of nanostructured scaffolds enables controlled multilineage differentiation of stem cells.Medicine. A comeback for gene therapy.De Novo proteome analysis of genetically modified tumor cells by a metabolic labeling/azide-alkyne cycloaddition approach.Development of poly(β-amino ester)-based biodegradable nanoparticles for nonviral delivery of minicircle DNA.Treatment of canine leukocyte adhesion deficiency by foamy virus vectors expressing CD18 from a PGK promoter.Targeted plasmid integration into the human genome by an engineered zinc-finger recombinaseRetroviral vector insertion sites associated with dominant hematopoietic clones mark "stemness" pathways.Gammaretroviral vector integration occurs overwhelmingly within and near DNase hypersensitive sitesCytokine-independent growth and clonal expansion of a primary human CD8+ T-cell clone following retroviral transduction with the IL-15 gene.Transcriptome Analysis of Targeted Mouse Mutations Reveals the Topography of Local Changes in Gene ExpressionMultilineage hematopoietic reconstitution without clonal selection in ADA-SCID patients treated with stem cell gene therapy.Ubiquitous high-level gene expression in hematopoietic lineages provides effective lentiviral gene therapy of murine Wiskott-Aldrich syndrome.Inhibition of autophagy by 3-MA enhances IL-24-induced apoptosis in human oral squamous cell carcinoma cellsHematopoietic stem-cell gene therapy of hemophilia A incorporating a porcine factor VIII transgene and nonmyeloablative conditioning regimens.Engineering lymphocyte subsets: tools, trials and tribulationsDelivery of siRNA via cationic Sterosomes to enhance osteogenic differentiation of mesenchymal stem cells.Internalization of Vectorized Liposomes Loaded with Plasmid DNA in C6 Glioma Cells.Stable gammaretroviral vector expression during embryonic stem cell-derived in vitro hematopoietic development.Reducing the genotoxic potential of retroviral vectors.The role of Rds in outer segment morphogenesis and human retinal disease.Vectors for airway gene delivery.
P2860
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P2860
Mutagenesis and oncogenesis by chromosomal insertion of gene transfer vectors.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh
2006年學術文章
@zh-hant
name
Mutagenesis and oncogenesis by chromosomal insertion of gene transfer vectors.
@ast
Mutagenesis and oncogenesis by chromosomal insertion of gene transfer vectors.
@en
type
label
Mutagenesis and oncogenesis by chromosomal insertion of gene transfer vectors.
@ast
Mutagenesis and oncogenesis by chromosomal insertion of gene transfer vectors.
@en
prefLabel
Mutagenesis and oncogenesis by chromosomal insertion of gene transfer vectors.
@ast
Mutagenesis and oncogenesis by chromosomal insertion of gene transfer vectors.
@en
P2093
P356
P1433
P1476
Mutagenesis and oncogenesis by chromosomal insertion of gene transfer vectors
@en
P2093
Christopher Baum
Olga Kustikova
Ute Modlich
Zhixiong Li
P304
P356
10.1089/HUM.2006.17.253
P50
P577
2006-03-01T00:00:00Z