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It inhibits both Type I and Type II isoenzymes, leading to a more significant reduction in DHT production
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(2025) used the CRISPR/Cas9 system to stably integrate SOX9 and TGF1 into the AAVS1 safe harbor locus of human MSCs, successfully engineering tonsil-derived MSCs (ToMSCs)
It can increase serum insulin and reduce blood glucose levels in diabetic mice [184]
