小头畸形
类有机物
清脆的
神经发育障碍
神经科学
生物
疾病
机制(生物学)
医学
基因
计算生物学
遗传学
病理
认识论
哲学
作者
Adriana Cherskov,Nenad Šestan
出处
期刊:Nature
[Springer Nature]
日期:2020-12-23
卷期号:589 (7840): 24-25
被引量:3
标识
DOI:10.1038/d41586-020-03636-z
摘要
A high-throughput technique has been developed to screen genes implicated in neurodevelopmental diseases in 3D cell cultures. It reveals a mechanism that might be involved in a rare disorder called microcephaly. A CRISPR-based organoid screen for genes involved in microcephaly.
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