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Author Spotlight: Exploring Macrophage Immunometabolism Through Lentiviral Vector-Mediated Gene Manipulation
Published on: February 16, 2024
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[A modular approach to in vivo gene therapy]
1Biologiste, généticien et immunologiste, Président d'Aprogène (Association pour la promotion de la Génomique), 13007 Marseille, France.
Summary
Gene editing successfully inactivated a harmful gene in vivo, showing excellent results in a small trial. This modular CRISPR-Cas9 gene therapy approach, using a modified guide RNA, offers potential for treating various genetic diseases.
Area of Science:
- Molecular Biology
- Genetics
- Biotechnology
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