摘要
Alzheimer's disease(AD)is a progressive neurodegenerative disorder causing memory loss,cognitive decline,language impairment,and disorientation,which impose an enormous burden on caregivers and the public health sector.A673T as a protective mutation has great therapeutic potential in AD.1,2 Therefore,a combination of stem cell therapy and A673T mutation existing in natural people based on gene targeting techniques such as CRISPR-Cas9 have been suggested as promising and exciting new developments.
基金
supported by the National Natural Science Foundation of China (No.81701078)
the Natural Science Foundation of Heilongjiang Province of China (Outstanding Youth Foundation,No.YQ2022H003)
China Postdoctoral Science Foundation (No.2016M600261,2018T110317)
Heilongjiang Postdoctoral Financial Assistance (China) (No.LBH-Z15163)
Heilongjiang Touyan Innovation Team Program (China).