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- W3207143416 abstract "In utero fetal therapy offers the opportunity to prevent and treat diseases with a cellular or genetic basis. Components of successful fetal treatment include isolation of a replacement cell population, in utero stem cell transplantation, cell engraftment with fetal immune tolerance, and ongoing cell function. Fetal gene therapy with CRISPR-Cas9 represents an exciting potential therapy for genetic diseases not amenable to gene supplementation via adenoviral vector transduction. These fetal therapies have unique ethical and safety considerations. Clinical trials for in utero cell therapy are underway, as additional discoveries in stem cell biology and gene therapy move closer to clinical translation." @default.
- W3207143416 created "2021-10-25" @default.
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- W3207143416 date "2021-10-21" @default.
- W3207143416 modified "2023-10-01" @default.
- W3207143416 title "In Utero Fetal Therapy: Stem Cells, Cell Transplantation, Gene Therapy, and CRISPR-Cas9" @default.
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- W3207143416 doi "https://doi.org/10.1097/grf.0000000000000663" @default.
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