Evaluating Efficiencies of Dual AAV Approaches for Retinal Targeting.

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Spliceosome-Mediated Pre-mRNA trans-Splicing Can Repair CEP290 mRNA.

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Evaluating Efficiencies of Dual AAV Approaches for Retinal Targeting.

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Evaluating Efficiencies of Dual AAV Approaches for Retinal Targeting.

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Evaluating Efficiencies of Dual AAV Approaches for Retinal Targeting.

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Evaluating Efficiencies of Dual AAV Approaches for Retinal Targeting.

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P1476

Evaluating Efficiencies of Dual AAV Approaches for Retinal Targeting.

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Heikki T Turunen

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Jean Bennett

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Luk H Vandenberghe

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María V Luna-Velez

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Ru Xiao

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Sarah J Wassmer

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P2860

Packaging capacity of adeno-associated virus serotypes: impact of larger genomes on infectivity and postentry steps.

Regulation of translation initiation in eukaryotes: mechanisms and biological targets

A hybrid vector system expands adeno-associated viral vector packaging capacity in a transgene-independent manner

Retinal gene therapy in patients with choroideremia: initial findings from a phase 1/2 clinical trial.

Relationship between mRNA stability and length: an old question with a new twist.

AAV recombineering with single strand oligonucleotides.

Effect of genome size on AAV vector packaging.

Development of an intein-mediated split-Cas9 system for gene therapy

Trans-splicing vectors expand the utility of adeno-associated virus for gene therapy.

In Silico Reconstruction of the Viral Evolutionary Lineage Yields a Potent Gene Therapy Vector

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scholarly article

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10.3389/FNINS.2017.00503

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Livia S. Carvalho

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2017-09-08T00:00:00Z

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28943836

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5596095

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Evaluating Efficiencies of Dual AAV Approaches for Retinal Targeting.

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P2860

P2860

Evaluating Efficiencies of Dual AAV Approaches for Retinal Targeting.

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P1476

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