Terminally maturing erythroblasts have dynamic changes in transcription-related chromatin modifications and RNA Polymerase II occupancy (ChIP-Seq 1)
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https://www.ncbi.nlm.nih.gov/sra/SRP276515
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资源简介：
We suggest a novel paradigm for understanding the epigenetic mechanisms that govern terminal erythroid maturation, and underlie inherited and acquired erythroid disease. Overall design: Two replicates of CD36 synchronization cultures at Day 7 and Day 10 are compared following ChIP-seq for RNA Pol II, or two replicates of early or late erythroblasts with appropriate controls
创建时间：
2022-01-12
