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Deep Parallel Characterization of AAV Tropism and AAV-Mediated Transcriptional Changes Single-Cell RNA Sequencing.
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AAV5 delivery of CRISPR-Cas9 supports effective genome editing in mouse lung airway.
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Optimization of lipid nanoparticles for the delivery of nebulized therapeutic mRNA to the lungs.
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Host genetics and infectious disease: new tools, insights and translational opportunities.
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Functionalized lipid-like nanoparticles for in vivo mRNA delivery and base editing.
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CRISPR Gene Therapy: Applications, Limitations, and Implications for the Future.
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Delivery of genome-editing biomacromolecules for treatment of lung genetic disorders.
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Synergistic lipid compositions for albumin receptor mediated delivery of mRNA to the liver.
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