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Genome Editing in Human iPS Cells to Study and Cure Disease

Human iPS (induced pluripotent stem) cells have the potential to allow us to study diseases in virtually any type of human cell, and develop cell transplantation-based therapies. Our team is developing and improving genome editing technology in iPS cells. We are developing novel isogenic iPS cell-based disease models, and correcting mutations in iPS cells from patients, a critical step in transplantation-based therapies. Our current focus is on diseases affecting cardiomyocytes and hepatocytes. →More

Upcoming

2025. 3. 20-22. 24th Congress of the Japanese Society for Regenerative Medicine @ Pacifico Yokohama

2025. 4. 15&16. RegMed2025 @Karolinska Institutet (Talk)

2025. 5. 28. Seminar @ Atsugi Campus of Tokyo University of Agriculture

2025. 6.11-14. ISSCR 2025 @HongKong

2025. 6.16-18. 10th Annual Meeting of The Japanese Society for Genome Editing

2025. 7.19-21. 32th The Bayer Scholarship for Cardiovascular Research Conference @Kochi

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