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Genomic analyses of TF binding, histone acetylation and gene expression reveal classes of E2-regulated promoters
PubMed Full text in PMC Similar studies Analyze with GEO2R
The role of PARP-1 in estrogen-dependent transcription
PubMed Full text in PMC Similar studies
The role of PARP-1 in estrogen-dependent transcription [RNA-seq]
PubMed Full text in PMC Similar studies Analyze with GEO2RSRA Run Selector
The role of PARP-1 in estrogen-dependent transcription [ChIP-seq]
PubMed Full text in PMC Similar studies SRA Run Selector
NAD+ Analog-sensitive PARPs Reveal a Role for PARP-1 in Transcription Elongation
Bromodomain-Containing-Protein 4 (BRD4) Regulates RNA Polymerase II Serine 2 Phosphorylation in Human CD4+ T Cells
U2OS-ERa, U2OS-ERb, and U2OS-ERab cells treated with 4HT or E2
PubMed Similar studies Analyze with GEO2R
Estrogen receptor alpha/beta heterodimer action in response to estrogen and tamoxifen
PubMed Similar studies GEO Profiles Analyze DataSet
Novel Estrogen Receptor-{alpha} Binding Sites and Estradiol Target Genes Identified by ChIP Cloning in Breast Cancer.
Estradiol effect on breast cancer cell line: time course
H4K12ac is regulated by estrogen receptor-alpha and is associated with BRD4 function and inducible transcription
H3Cit26 ChIP-chip from MCF-7 cells
Non-linear relationship between chromatin accessibility and estradiol-regulated gene expression
PubMed Similar studies Analyze with GEO2RSRA Run Selector
Estrogen regulation and physiopathologic significance of alternative promoters in breast cancer
ChIP-Seq of ERalpha and RNA polymerase II defines genes differentially responding to ligands
Coativator Function Defines the Active Estrogen Receptor Alpha Cistrome
The histone variant H2A.Z is an important regulator of enhancer activity.
Target Gene Repression Based on Dismissal of Polymerase II from Estrogen Receptor Trans-bound Enhancers Is Associated With Clinical Outcome in Human Breast Cancer
Target Gene Repression Based on Dismissal of Polymerase II from Estrogen Receptor Trans-bound Enhancers Is Associated With Clinical Outcome in Human Breast Cancer [GRO-seq]
Target Gene Repression Based on Dismissal of Polymerase II from Estrogen Receptor Trans-bound Enhancers Is Associated With Clinical Outcome in Human Breast Cancer [ChIP-seq]
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