Avoiding cytotoxicity of transposases by dose-controlled mRNA delivery
about
Recombinant messenger RNA technology and its application in cancer immunotherapy, transcript replacement therapies, pluripotent stem cell induction, and beyondRetroviral vectors and transposons for stable gene therapy: advances, current challenges and perspectivesDriving DNA transposition by lentiviral protein transductionDNA transposon-based gene vehicles - scenes from an evolutionary driveGammaretroviral vectors: biology, technology and applicationEffective gene trapping mediated by Sleeping Beauty transposon.An efficient low cost method for gene transfer to T lymphocytesInfluence of untranslated regions on retroviral mRNA transfer and expressionGenomic analysis of Sleeping Beauty transposon integration in human somatic cells.Efficient transient genetic manipulation in vitro and in vivo by prototype foamy virus-mediated nonviral RNA transferSleeping Beauty Transposon Vectors in Liver-directed Gene Delivery of LDLR and VLDLR for Gene Therapy of Familial HypercholesterolemiaIntegration profile and safety of an adenovirus hybrid-vector utilizing hyperactive sleeping beauty transposase for somatic integration.DNA transposition by protein transduction of the piggyBac transposase from lentiviral Gag precursorsThe Sleeping Beauty transposon system for clinical applications.Recent developments in transposon-mediated gene therapy.Technological overview of iPS induction from human adult somatic cells.Non-integrating gamma-retroviral vectors as a versatile tool for transient zinc-finger nuclease delivery.Viral and Synthetic RNA Vector Technologies and Applications.Sleeping Beauty transposition: from biology to applications.Transposon-mediated Generation of Cellular and Mouse Models of Splicing Mutations to Assess the Efficacy of snRNA-based TherapeuticsGoing non-viral: the Sleeping Beauty transposon system breaks on through to the clinical side.Prevention of Allograft Rejection by Use of Regulatory T Cells With an MHC-Specific Chimeric Antigen Receptor.Stem cell models of polyglutamine diseases and their use in cell-based therapies.Deciphering the impact of parameters influencing transgene expression kinetics after repeated cell transduction with integration-deficient retroviral vectors.Vector modifications to eliminate transposase expression following piggyBac-mediated transgenesisFeeder-free reprogramming of human fibroblasts with messenger RNA.Transcriptionally regulated and nontoxic delivery of the hyperactive Sleeping Beauty Transposase.Gateway-compatible transposon vector to genetically modify human embryonic kidney and adipose-derived stromal cells.An Efficient In Vitro Transposition Method by a Transcriptionally Regulated Sleeping Beauty System Packaged into an Integration Defective Lentiviral Vector.Transient Retrovirus-Based CRISPR/Cas9 All-in-One Particles for Efficient, Targeted Gene Knockout
P2860
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P2860
Avoiding cytotoxicity of transposases by dose-controlled mRNA delivery
description
2011 nî lūn-bûn
@nan
2011 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Avoiding cytotoxicity of transposases by dose-controlled mRNA delivery
@ast
Avoiding cytotoxicity of transposases by dose-controlled mRNA delivery
@en
type
label
Avoiding cytotoxicity of transposases by dose-controlled mRNA delivery
@ast
Avoiding cytotoxicity of transposases by dose-controlled mRNA delivery
@en
prefLabel
Avoiding cytotoxicity of transposases by dose-controlled mRNA delivery
@ast
Avoiding cytotoxicity of transposases by dose-controlled mRNA delivery
@en
P2093
P2860
P50
P356
P1476
Avoiding cytotoxicity of transposases by dose-controlled mRNA delivery
@en
P2093
Christine S Falk
Christopher Baum
Daniela Zychlinski
Gudrun Göhring
Johannes Kuehle
Kathrin Lange
Martijn H Brugman
Melanie Galla
Niels Heinz
Tobias Maetzig
P2860
P304
P356
10.1093/NAR/GKR384
P407
P577
2011-05-23T00:00:00Z