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In vivo neuronal gene editing via CRISPR-Cas9 amphiphilic nanocomplexes alleviates deficits in mouse models of Alzheimer's disease
- Park, Hanseul;
- Oh, Jungju;
- Shim, Gayong;
- Cho, Byounggook;
- Chang, Yujung;
- ... Lee, Minhyung;
- 외 11명
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In vivo gene editing in post-mitotic neurons of the adult brain may be a useful strategy for treating neurological diseases. Here, we develop CRISPR-Cas9 nanocomplexes and show they were effective in the adult mouse brain, with minimal off-target effects. Using this system to target Bacel suppressed amyloid beta (A beta)-associated pathologies and cognitive deficits in two mouse models of Alzheimer's disease. These results broaden the potential application of CRISPR-Cas9 systems to neurodegenerative diseases.
키워드
MICE; EXPRESSION; PROTEIN; MUSCLE
- 제목
- In vivo neuronal gene editing via CRISPR-Cas9 amphiphilic nanocomplexes alleviates deficits in mouse models of Alzheimer's disease
- 저자
- Park, Hanseul; Oh, Jungju; Shim, Gayong; Cho, Byounggook; Chang, Yujung; Kim, Siyoung; Baek, Soonbong; Kim, Hongwon; Shin, Jeain; Choi, Hwan; Yoo, Junsang; Kim, Junyeop; Jun, Won; Lee, Minhyung; Lengner, Christopher J.; Oh, Yu-Kyoung; Kim, Jongpil
- 발행일
- 2019-04
- 유형
- Article
- 권
- 22
- 호
- 4
- 페이지
- 524 ~ 528