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Estradiol effect on breast cancer cell line in the absence of protein synthesis
PubMed Full text in PMC Similar studies GEO Profiles Analyze DataSet
Gene expression analysis of hormone treated MCF7 breast cancer cells in the presence or absence of cycloheximide
PubMed Full text in PMC Similar studies Analyze with GEO2R
Nuclear and Extranuclear Pathway Inputs in the Regulation of Global Gene Expression by Estrogen Receptors
Genomic analyses of TF binding, histone acetylation and gene expression reveal classes of E2-regulated promoters
Novel Estrogen Receptor-{alpha} Binding Sites and Estradiol Target Genes Identified by ChIP Cloning in Breast Cancer.
PubMed Similar studies Analyze with GEO2R
Estradiol effect on breast cancer cell line: time course
PubMed Similar studies GEO Profiles Analyze DataSet
Distinct Roles of BET Family Members in ERα Enhancer Function and Gene Regulation in Breast Cancer Cells
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Distinct roles of BET Family Members in ERα Enhancer Function and Gene Regulation in Breast Cancer Cells [ChIP-seq]
PubMed Full text in PMC Similar studies SRA Run Selector
Distinct Roles of BET Family Members in ERα Enhancer Function and Gene Regulation in Breast Cancer Cells [RNA-seq]
PubMed Full text in PMC Similar studies Analyze with GEO2RSRA Run Selector
Gene Regulation by Estrogen Signaling and DNA Methylation in MCF7 Breast Cancer Cells
Estrogen regulation and physiopathologic significance of alternative promoters in breast cancer
Estrogen effects on MCF-7 breast cancer cells co-expressing ERa and ERb
Estrogen effect on breast cancer cell line coexpressing estrogen receptors alpha and beta
Genomic analyses of breast cancer cells: 17β-hydroxysteroid dehydrogenase type 1 induces transcriptional changes in estradiol-dependent and independent manners
A hypermethylation strategy utilized by enhancer-bound CARM1 to promote estrogen receptor a-dependent transcriptional activation and breast carcinogenesis
A hypermethylation strategy utilized by enhancer-bound CARM1 to promote estrogen receptor a-dependent transcriptional activation and breast carcinogenesis (ChIP-Seq)
A hypermethylation strategy utilized by enhancer-bound CARM1 to promote estrogen receptor a-dependent transcriptional activation and breast carcinogenesis (RNA-seq)
Transient ER binding and p300 redistribution support a physiological squelching model for immediate ER-repressed genes
Distinct properties of cell type-specific and shared transcription factor binding sites
Transcription Factor Binding Sites by ChIP-seq from ENCODE/HAIB
PubMed Full text in PMC Similar studies ENCODESRA Run Selector
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