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Updated: May 23, 2026

Packaging HIV- or FIV-based Lentivector Expression Constructs & Transduction of VSV-G Pseudotyped Viral Particles
Published on: April 8, 2012
Toshie Sakuma1, Michael A Barry, Yasuhiro Ikeda
1Department of Molecular Medicine, Mayo Clinic College of Medicine, 200 First Street SW, Rochester, MN 55905, USA.
Lentiviral vectors, evolved from modified HIV, offer safe and efficient gene delivery. These vectors stably integrate genes into host cells, enabling diverse applications in research and therapy.
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