Dissecting developmental disorders caused by CTCF mutation at R567 [ChIP-seq]. Dissecting developmental disorders caused by CTCF mutation at R567 [ChIP-seq]
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下载链接：
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA886685
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资源简介：
In this study, CTCF ChIP experiments were performed to investigate the influence of CTCF mutation on its binding in mouse tissues. Overall design: ChIP-seq for CTCF in tissues from wild-type and Ctcf homozygous mutated E18.5 mouse embryos.
创建时间：
2022-10-03
