CTCF point mutation at R567 disrupts mouse heart development via 3D genome rearrangement and transcription dysregulation [4C-seq]
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https://www.ncbi.nlm.nih.gov/sra/SRP531364
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资源简介：
In this study, we performed 4C sequencing to investigate alterations in chromatin interactions mediated by the Lmod2 promoter and its potential enhancer. Overall design: 4C-seq was performed using wild-type and Ctcf homozygous mutation in heart tissues from E18.5 mouse embryos. The region for Lmod2 promoter and its potential enhancer was used as a viewpoint.
创建时间：
2025-04-10
