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Updated: Apr 4, 2026

09:51
Establishment of Genome-edited Human Pluripotent Stem Cell Lines: From Targeting to Isolation
Published on: February 2, 2016
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[Genetic manipulation of stem cells]
1Division of Genetic Therapeutics, Jichi Medical University.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology
|September 9, 2015
Summary
Genetic engineering using adeno-associated virus (AAV) enables site-specific DNA insertion into the AAVS1 locus, minimizing cancer risks. This safe harbor approach is ideal for stem cell therapies and large DNA insertions.
Area of Science:
- Molecular Biology
- Gene Therapy
- Genetics
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