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Pre-existing anti-adeno-associated virus antibodies as a challenge in AAV gene therapy - 2013.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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Pharmacological modulation of humoral immunity in a nonhuman primate model of AAV gene transfer for hemophilia B - 2012.pdf
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Programmable genome editing tools and their regulation for efficient genome engineering - 2017.pdf
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Overview of gene therapy and viral vectors for CNS applications - Martha Bohn - 2005.pdf
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Progress towards in vivo use of siRNAs.pdf
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Overcoming preexisting humoral immunity to AAV using capsid decoys - 2013.pdf
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Retrovirus-mediated single-cell gene knockout technique in adult newborn neurons in vivo.pdf
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Optimization of PAMAM-gold nanoparticle conjugation for gene therapy - 2015.pdf
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Safety and efficacy of gene transfer for Leber's congenital amaurosis.pdf
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Non-viral vectors for gene-based therapy - review - 2014.pdf
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Strategies to circumvent humoral immunity to adeno-associated viral vectors - 2015.pdf
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Non-viral nucleic acid delivery strategies to the central nervous system - 2016.pdf
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Structure-guided evolution of antigenically distinct adeno-associated virus variants for immune evasion - 2017.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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Systemic gene delivery to the central nervous system using Adeno-associated virus - 2014.pdf
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Nanoparticles as a tool for transfection and transgenesis - A review - 2016.pdf
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Targeted plasmid integration into the human genome by an engineered zinc-finger recombinase - 2011.pdf
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Mechanisms and strategies for effective delivery of antisense and siRNA - 2008.pdf
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The ideal gene delivery vector: Chromallocytes, cell repair nanorobots for chromosome replacement therapy - Freitas - 2007.pdf
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Therapeutic application of RNAi - is mRNA targetting finally ready for the prime time - 2007.pdf
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