Development of a novel helper-dependent adenovirus-Epstein-Barr virus hybrid system for the stable transformation of mammalian cells.
about
Adenoviral vector immunity: its implications and circumvention strategies.In vivo stable transduction of humanized liver tissue in chimeric mice via high-capacity adenovirus-lentivirus hybrid vector.Development of a hybrid baculoviral vector for sustained transgene expressionStable transgene expression in primitive human CD34+ hematopoietic stem/progenitor cells, using the Sleeping Beauty transposon systemWhen Cre-mediated recombination in mice does not result in protein loss.LDLR-Gene therapy for familial hypercholesterolaemia: problems, progress, and perspectivesCurrent strategies and future directions for eluding adenoviral vector immunityDelivery of an EBV episome by a self-circularizing helper-dependent adenovirus: long-term transgene expression in immunocompetent mice.Hybrid adeno-associated viral vectors utilizing transposase-mediated somatic integration for stable transgene expression in human cells.Versatility of gene therapy vectors through viruses.Targeting site-specific chromosome integration.Helper-dependent adenoviral vectors in experimental gene therapy.A rapid Q-PCR titration protocol for adenovirus and helper-dependent adenovirus vectors that produces biologically relevant results.Enhanced Generation of Integration-free iPSCs from Human Adult Peripheral Blood Mononuclear Cells with an Optimal Combination of Episomal Vectors.Enhanced and prolonged baculovirus-mediated expression by incorporating recombinase system and in cis elements: a comparative studyRobust in vivo transduction of a genetically stable Epstein-Barr virus episome to hepatocytes in mice by a hybrid viral vectorCellular reprogramming of human peripheral blood cellsHigh-level expression by tissue/cancer-specific promoter with strict specificity using a single-adenoviral vector.A rapid protocol for construction and production of high-capacity adenoviral vectors.Generation of Integration-free Induced Pluripotent Stem Cells from Human Peripheral Blood Mononuclear Cells Using Episomal Vectors.A Novel Adenoviral Hybrid-vector System Carrying a Plasmid Replicon for Safe and Efficient Cell and Gene Therapeutic Applications.Novel HDAd/EBV Reprogramming Vector and Highly Efficient Ad/CRISPR-Cas Sickle Cell Disease Gene Correction.
P2860
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P2860
Development of a novel helper-dependent adenovirus-Epstein-Barr virus hybrid system for the stable transformation of mammalian cells.
description
2004 nî lūn-bûn
@nan
2004 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Development of a novel helper- ...... sformation of mammalian cells.
@ast
Development of a novel helper- ...... sformation of mammalian cells.
@en
Development of a novel helper- ...... sformation of mammalian cells.
@nl
type
label
Development of a novel helper- ...... sformation of mammalian cells.
@ast
Development of a novel helper- ...... sformation of mammalian cells.
@en
Development of a novel helper- ...... sformation of mammalian cells.
@nl
prefLabel
Development of a novel helper- ...... sformation of mammalian cells.
@ast
Development of a novel helper- ...... sformation of mammalian cells.
@en
Development of a novel helper- ...... sformation of mammalian cells.
@nl
P2093
P2860
P1433
P1476
Development of a novel helper- ...... sformation of mammalian cells.
@en
P2093
Arnold J Berk
Brenton T Tan
Jose S Gil
Maria G Castro
Michele P Calos
Oliver Dorigo
Pedro R Lowenstein
Sean D Gallaher
P2860
P304
P356
10.1128/JVI.78.12.6556-6566.2004
P407
P577
2004-06-01T00:00:00Z