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CRISPR Delivery Systems and In Vivo Gene Therapy Development

Genetics
CRISPR Gene Editing Applications Research
CRISPR Delivery Systems and In Vivo Gene Therapy Development
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GeneticsCRISPR Gene Editing Applications Research

CRISPR Delivery Systems and In Vivo Gene Therapy Development

Interns will research and evaluate delivery mechanisms for CRISPR components including viral vectors (AAV, lentivirus) and non-viral carriers (lipid nanoparticles, exosomes) for therapeutic applications. Work will include characterizing transfection efficiency, cellular uptake pathways, and immunogenicity in relevant disease models.

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