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Knockdown of ASD risk genes leads to a shared transcriptional signature. Knockdown of ASD risk genes leads to a shared transcriptional signature

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NIAID Data Ecosystem2026-03-13 收录
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https://www.ncbi.nlm.nih.gov/bioproject/PRJNA797092
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资源简介:
RNAseq analysis of shRNA-mediated knockdown of chromatin modifiers associated with Autism Spectrum Disorder Overall design: E16.5 primary cortical neurons were cultured for 5 days before infection by shRNAs targeting one of Ash1L, Chd8, Crebbp, Ehmt1, Nsd1, Gtf2i, or Luciferase. Neurons were cultured for 5 additional days before RNA was collected.

针对自闭症谱系障碍相关染色质调控因子的短发夹RNA(shRNA)介导敲低的RNA测序(RNAseq)分析。实验整体设计:将胚胎16.5天(E16.5)的原代皮层神经元体外培养5天后,使用靶向Ash1L、Chd8、Crebbp、Ehmt1、Nsd1、Gtf2i或荧光素酶(Luciferase)的shRNA进行感染。随后继续培养神经元5天,再收集RNA样本。
创建时间:
2022-01-13
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