Found: 12
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Measles virus selectively blind to signaling lymphocyte activation molecule as a novel oncolytic virus for breast cancer treatment.
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- Gene Therapy, 2013, v. 20, n. 3, p. 338, doi. 10.1038/gt.2012.44
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- Article
Axonal transport of adeno-associated viral vectors is serotype-dependent.
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- Gene Therapy, 2013, v. 20, n. 3, p. 348, doi. 10.1038/gt.2012.27
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- Article
Anti-angiogenic therapy increases intratumoral adenovirus distribution by inducing collagen degradation.
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- Gene Therapy, 2013, v. 20, n. 3, p. 318, doi. 10.1038/gt.2012.42
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- Article
A calcium-sensitive promoter construct for gene therapy.
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- Gene Therapy, 2013, v. 20, n. 3, p. 248, doi. 10.1038/gt.2012.30
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- Article
Therapeutic antitumor potential of endoglin-based DNA vaccine combined with immunomodulatory agents.
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- Gene Therapy, 2013, v. 20, n. 3, p. 262, doi. 10.1038/gt.2012.28
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- Article
MRI roadmap-guided transendocardial delivery of exon-skipping recombinant adeno-associated virus restores dystrophin expression in a canine model of Duchenne muscular dystrophy.
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- Gene Therapy, 2013, v. 20, n. 3, p. 274, doi. 10.1038/gt.2012.38
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- Article
Endocytic processing of adeno-associated virus type 8 vectors for transduction of target cells.
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- Gene Therapy, 2013, v. 20, n. 3, p. 308, doi. 10.1038/gt.2012.41
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- Article
Using clinically approved cyclophosphamide regimens to control the humoral immune response to oncolytic viruses.
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- Gene Therapy, 2013, v. 20, n. 3, p. 255, doi. 10.1038/gt.2012.31
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- Article
Distinct transduction difference between adeno-associated virus type 1 and type 6 vectors in human polarized airway epithelia.
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- Gene Therapy, 2013, v. 20, n. 3, p. 328, doi. 10.1038/gt.2012.46
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- Article
Efficient in vivo regulation of cytidine deaminase expression in the haematopoietic system using a doxycycline-inducible lentiviral vector system.
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- Gene Therapy, 2013, v. 20, n. 3, p. 298, doi. 10.1038/gt.2012.40
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- Article
Gene transfer in inner ear cells: a challenging race.
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- Gene Therapy, 2013, v. 20, n. 3, p. 237, doi. 10.1038/gt.2012.51
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- Article
Sstr2A: a relevant target for the delivery of genes into human glioblastoma cells using fiber-modified adenoviral vectors.
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- Gene Therapy, 2013, v. 20, n. 3, p. 283, doi. 10.1038/gt.2012.39
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- Article