首页/数据集/FoxA1 specifies unique androgen and glucocorticoid receptor binding events in prostate cancer cells (mRNA)

FoxA1 specifies unique androgen and glucocorticoid receptor binding events in prostate cancer cells (mRNA)

ChEBI2013-02-05 更新2026-07-21 收录

癌症转录调控

激素受体信号通路

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-39654 数据链接链接失效反馈

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资源简介：

FoxA1 specifies unique androgen and glucocorticoid receptor binding events in prostate cancer cells (mRNA)

应用场景：

创建时间：

2013-02-05

癌症转录调控

恶性肿瘤分子机制

This SuperSeries is composed of the following subset Series: GSE38232: HSF1 drives a transcriptional program distinct from heat shock to support highly malignant human cancers [gene expression] GSE389

NIAID Data Ecosystem90

Proteasome inhibition blocks estrogen-dependent gene transcription by decreasing histone H2B monoubiquitination in human breast cancer cells. Homo sapiens

癌症转录调控

蛋白酶体抑制

The estrogen receptor-alpha (ERα) determines breast cancer cell phenotype and is a prognostic indicator. A better understanding of the mechanisms controlling ERα function may uncover improved strategi

NIAID Data Ecosystem40

Convergence of oncogenic and hormone receptor pathways promotes pro-metastatic phenotypes.

癌症转移机制

激素受体信号通路

Convergence of oncogenic and hormone receptor pathways promotes pro-metastatic phenotypes.

ChEBI2013-03-31 更新00

Genome-wide AR binding under androgen deprivation condition upon TRAF4 overexpression. Genome-wide AR binding under androgen deprivation condition upon TRAF4 overexpression

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全基因组结合位点分析

We report that TRAF4-mediated AR ubiquitination alters AR genomic binding profile under androgen deprivation condition. Overall design: Examination of AR genome-wide binding in control and TRAF4 overe

NIAID Data Ecosystem50

Time-course effect of estradiol and ERa17p on Early Gene expression in SKBR3 cells

乳腺细胞分子机制

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Time-course effect of estradiol and ERa17p on Early Gene expression in SKBR3 cells

ChEBI2012-07-30 更新20