随后, the researchers reprogrammed the disease-causing gene defects in the stem cells using the CRISPR-Cas9 technique, known as gene scissors. 最后, the researchers guided the corrected stem cells to differentiate into liver cells to see whether the disease that impairs hepatic function was actually cured and that the fixed cells no longer produced the harmful argininosuccinic acid.
干细胞疗法
肝脏干细胞疗法
失代偿期肝硬化患者大多不得不选择肝移植, 但捐献器官的供应有限且成本高昂导致等待名单上的死亡率很高 . 自己身体的干细胞有帮助 阅读更多…