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Long-term gene expression and phenotypic correction using adeno-associated virus vectors in the mammalian brain - 1994.pdf

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Long-term gene expression and phenotypic correction using adeno-associated virus vectors in the mammalian brain - 1994.pdf
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In vivo selection yields AAV-B1 capsid for central nervous system and muscle gene therapy - 2016.pdf
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Mechanisms and strategies for effective delivery of antisense and siRNA - 2008.pdf
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Nanoparticles as a tool for transfection and transgenesis - A review - 2016.pdf
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Intensive pharmacological immunosuppression allows for repetitive liver gene transfer with recombinant adenovirus in nonhuman primates - 2010.pdf
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Naturally enveloped AAV vectors for shielding neutralizing antibodies and robust gene delivery in vivo - 2014.pdf
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Immune responses to AAV vectors: overcoming barriers to successful gene therapy - 2013.pdf
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Non-viral nucleic acid delivery strategies to the central nervous system - 2016.pdf
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Non-viral vectors for gene-based therapy - review - 2014.pdf
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Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics.pdf
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How to name and classify your phage: an informal guide - 2017.pdf
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Optimization of PAMAM-gold nanoparticle conjugation for gene therapy - 2015.pdf
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Genome-editing technologies for gene and cell therapy - 2016.pdf
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Overcoming preexisting humoral immunity to AAV using capsid decoys - 2013.pdf
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Gene transfer in humans using a conditionally replicating lentiviral vector.pdf
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Overview of gene therapy and viral vectors for CNS applications - Martha Bohn - 2005.pdf
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Pharmacological modulation of humoral immunity in a nonhuman primate model of AAV gene transfer for hemophilia B - 2012.pdf
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Gene therapy using adeno-associated virus vectors - 2008.pdf
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Pre-existing anti-adeno-associated virus antibodies as a challenge in AAV gene therapy - 2013.pdf
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Programmable genome editing tools and their regulation for efficient genome engineering - 2017.pdf
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