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- W4380853560 abstract "Prader-Willi syndrome (PWS) is a neurodevelopmental disorder caused by loss of paternal expression of imprinted genes on chromosome 15q11-q13. We established a human induced pluripotent stem cell line (hiPSC), ZIPi021-A, from fibroblasts of a 4-year-old female PWS patient with the subtype of maternal uniparental disomy (mUPD). The generated hiPSC line was transgene-free, expressed pluripotency markers and showed the ability to differentiate into all three germ layers in vitro. The ZIPi021-A hiPSC line could be used as a cellular model for PWS in humans." @default.
- W4380853560 created "2023-06-16" @default.
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- W4380853560 date "2023-09-01" @default.
- W4380853560 modified "2023-10-16" @default.
- W4380853560 title "Generation of an induced pluripotent stem cell line, ZIPi021-A, from fibroblasts of a Prader-Willi syndrome patient with maternal uniparental disomy (mUPD)" @default.
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- W4380853560 doi "https://doi.org/10.1016/j.scr.2023.103143" @default.
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