基本信息
浏览量:0
职业迁徙
个人简介
Research interests
Genetic neurological disorders are challenging to treat, let alone cure due to the complexity of the brain and the barrier imposed by the blood brain barrier. Our research team are testing gene therapies, including gene editing technologies such as CRISPR gene editing tools to create novel therapies which have the capacity to cross the blood brain barrier and permanently correct mutated genes back to wild type in neuronal cells.To test this our lab uses mouse and cellular models including 2D neuronal cultures and 3D brain organoids.
Genetic neurological disorders are challenging to treat, let alone cure due to the complexity of the brain and the barrier imposed by the blood brain barrier. Our research team are testing gene therapies, including gene editing technologies such as CRISPR gene editing tools to create novel therapies which have the capacity to cross the blood brain barrier and permanently correct mutated genes back to wild type in neuronal cells.To test this our lab uses mouse and cellular models including 2D neuronal cultures and 3D brain organoids.
研究兴趣
论文共 56 篇作者统计合作学者相似作者
按年份排序按引用量排序主题筛选期刊级别筛选合作者筛选合作机构筛选
时间
引用量
主题
期刊级别
合作者
合作机构
Artur Shvetcov, Shannon Thomson,Jessica Spathos,Ann-Na Cho,Heather M. Wilkins,Shea J. Andrews,Fabien Delerue,Timothy A. Couttas, Jasmeen Kaur Issar,Finula Isik, Simranpreet Kaur,Eleanor Drummond,
Genetics in Medicine Openno. 1 (2023): 100220-100220
引用0浏览0引用
0
0
Ehud Banne, Baraa Abudiab, Sara Abu-Swai,Srinivasa Rao Repudi,Daniel J. Steinberg, Diala Shatleh,Sarah Alshammery,Leszek Lisowski,Wendy Gold,Peter L. Carlen,Rami I. Aqeilan
CELLSno. 4 (2021): 824
加载更多
作者统计
合作学者
合作机构
D-Core
- 合作者
- 学生
- 导师
数据免责声明
页面数据均来自互联网公开来源、合作出版商和通过AI技术自动分析结果,我们不对页面数据的有效性、准确性、正确性、可靠性、完整性和及时性做出任何承诺和保证。若有疑问,可以通过电子邮件方式联系我们:report@aminer.cn