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Tissue-specific CTCF/Cohesin-mediated chromatin architecture delimits enhancer interactions and function in vivo (Capture-C"
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Tissue-specific CTCF/Cohesin-mediated chromatin architecture delimits enhancer interactions and function in vivo
PubMed Full text in PMC Similar studies
Tissue-specific CTCF/Cohesin-mediated chromatin architecture delimits enhancer interactions and function in vivo (RNA-Seq)
Tissue-specific CTCF/Cohesin-mediated chromatin architecture delimits enhancer interactions and function in vivo (ChIP-Seq)
Tissue-specific CTCF/Cohesin-mediated chromatin architecture delimits enhancer interactions and function in vivo (ATAC-Seq)
CTCF and Cohesin link sex-biased distal regulatory elements to sex-biased gene expression in mouse liver
4C-seq analysis of interactions with promoters and enhancers nearby five sex-specific genes, in male and female mouse liver
CTCF and Cohesin (Rad21) ChIP-seq in female mouse liver
Computational prediction of CTCF/cohesin-based intra-TAD (sbTAD) loops that insulate chromatin contacts and gene expression in mouse liver
CTCF and Cohesin (Rad21) ChIP-seq in male mouse liver
Activation of the alpha-globin gene expression correlates with dramatic upregulation of nearby non-globin genes and changes of local and large-scale chromatin spatial structure
4C-seq analysis of interactions with the Albumin promoter in mouse liver
Genome architecture in definitive erythroid cells at base-pair resolution
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Defining genome architecture at base-pair resolution
Multiple CTCF sites contribute to stable enhancer-promoter interactions in the β-globin locus
CTCF and CohesinSA-1 Mark Active Promoters and Boundaries of Repressive Chromatin Domains in Primary Human Erythroid Cells
CTCF and CohesinSA-1 Mark Active Promoters and Boundaries of Repressive Chromatin Domains in Primary Human Erythroid Cells [RNA-Seq]
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CTCF and CohesinSA-1 Mark Active Promoters and Boundaries of Repressive Chromatin Domains in Primary Human Erythroid Cells [ChIP-Seq]
Specific contributions of cohesin-SA1 and cohesin-SA2 to TADs and Polycomb domains in embryonic stem cells.
Functional dissection of regulatory landscapes reveals non-essential and instructive roles of TADs in regulating gene expression
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