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Antibody neutralization poses a barrier to intravitreal adeno-associated viral vector gene delivery to non-human primates.
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- Gene Therapy, 2015, v. 22, n. 2, p. 116, doi. 10.1038/gt.2014.115
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- Article
Retinoschisin gene therapy in photoreceptors, Müller glia or all retinal cells in the Rs1h−/− mouse.
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- Gene Therapy, 2014, v. 21, n. 6, p. 585, doi. 10.1038/gt.2014.31
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- Article
Engineering a serum-resistant and thermostable vesicular stomatitis virus G glycoprotein for pseudotyping retroviral and lentiviral vectors.
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- Gene Therapy, 2013, v. 20, n. 8, p. 807, doi. 10.1038/gt.2013.1
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- Article
Directed evolution of novel adeno-associated viruses for therapeutic gene delivery.
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- Gene Therapy, 2012, v. 19, n. 6, p. 694, doi. 10.1038/gt.2012.20
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- Article
Enhanced gene delivery to the neonatal retina through systemic administration of tyrosine-mutated AAV9.
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- Gene Therapy, 2012, v. 19, n. 2, p. 176, doi. 10.1038/gt.2011.163
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- Article
Surface immobilization of hexa-histidine-tagged adeno-associated viral vectors for localized gene delivery.
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- Gene Therapy, 2010, v. 17, n. 11, p. 1384, doi. 10.1038/gt.2010.81
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- Article
Antiviral RNAi therapy: emerging approaches for hitting a moving target.
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- Gene Therapy, 2006, v. 13, n. 6, p. 532, doi. 10.1038/sj.gt.3302645
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- Article
Regulation of endogenous transmembrane receptors through optogenetic Cry2 clustering.
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- Nature Communications, 2015, v. 6, n. 4, p. 6898, doi. 10.1038/ncomms7898
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- Article