Works matching IS 09697128 AND DT 2013 AND VI 20 AND IP 6
Results: 12
Hairpin-end conformation of adeno-associated virus genome determines interactions with DNA-repair pathways.
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- Gene Therapy, 2013, v. 20, n. 6, p. 686, doi. 10.1038/gt.2012.86
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- Article
Quantification of HSV-1-mediated expression of the ferritin MRI reporter in the mouse brain.
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- Gene Therapy, 2013, v. 20, n. 6, p. 589, doi. 10.1038/gt.2012.70
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- Article
Generation of an optimized lentiviral vector encoding a high-expression factor VIII transgene for gene therapy of hemophilia A.
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- Gene Therapy, 2013, v. 20, n. 6, p. 607, doi. 10.1038/gt.2012.76
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- Article
scAAV-mediated gene transfer of interleukin-1-receptor antagonist to synovium and articular cartilage in large mammalian joints.
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- Gene Therapy, 2013, v. 20, n. 6, p. 670, doi. 10.1038/gt.2012.81
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- Article
In vivo delivery of DN:REST improves transcriptional changes of REST-regulated genes in HD mice.
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- Gene Therapy, 2013, v. 20, n. 6, p. 678, doi. 10.1038/gt.2012.84
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- Article
Sodium iodide symporter (NIS)-mediated radiovirotherapy of hepatocellular cancer using a conditionally replicating adenovirus.
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- Gene Therapy, 2013, v. 20, n. 6, p. 625, doi. 10.1038/gt.2012.79
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- Article
Highly acetylated tubulin permits enhanced interactions with and trafficking of plasmids along microtubules.
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- Gene Therapy, 2013, v. 20, n. 6, p. 616, doi. 10.1038/gt.2012.77
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- Article
Effective antitumor gene therapy delivered by polyethylenimine-conjugated stearic acid-g-chitosan oligosaccharide micelles.
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- Gene Therapy, 2013, v. 20, n. 6, p. 597, doi. 10.1038/gt.2012.72
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- Article
Design of T-cell receptor libraries with diverse binding properties to examine adoptive T-cell responses.
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- Gene Therapy, 2013, v. 20, n. 6, p. 634, doi. 10.1038/gt.2012.80
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- Article
Efficient gene expression from integration-deficient lentiviral vectors in the spinal cord.
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- Gene Therapy, 2013, v. 20, n. 6, p. 645, doi. 10.1038/gt.2012.78
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- Article
Understanding lentiviral vector chromatin targeting: working to reduce insertional mutagenic potential for gene therapy.
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- Gene Therapy, 2013, v. 20, n. 6, p. 581, doi. 10.1038/gt.2012.88
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- Publication type:
- Article
Systemic delivery of triplex-forming PNA and donor DNA by nanoparticles mediates site-specific genome editing of human hematopoietic cells in vivo.
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- Gene Therapy, 2013, v. 20, n. 6, p. 658, doi. 10.1038/gt.2012.82
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- Article