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LncRNA-dependent mechanisms of androgen receptor-regulated gene activation programs [GRO-seq II]

ChEBI2013-08-15 更新2026-07-21 收录

激素受体信号通路

LncRNA功能机制

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-47806 数据链接链接失效反馈

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资源简介：

LncRNA-dependent mechanisms of androgen receptor-regulated gene activation programs [GRO-seq II]

应用场景：

创建时间：

2013-08-15

激素受体信号通路

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

GR and ER co-activation alters the expression of differentiation genes and associates with improved ER+ breast cancer outcome

乳腺癌分子机制

激素受体信号通路

Analysis of MCF-7 cells treated for 4h with Ethanol, Estradiol (E2), Dexamethasone (Dex), or Estradiol + Dexamethasone (E2 + Dex) In estrogen receptor (ER)-negative breast cancer (BC), high tumor glu

NIAID Data Ecosystem30

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

Transcriptome analyses of AR stimulated by 0.1 nM or 10 nM DHT in LNCaP stable cell line overexpressing AR [RNA-Seq]. Transcriptome analyses of AR stimulated by 0.1 nM or 10 nM DHT in LNCaP stable cell line overexpressing AR [RNA-Seq]

前列腺癌分子机制

激素受体信号通路

The molecular drivers for the AR signaling reprogramming in castration-resistant prostate cancer remain to be determined. In this study, we hypothesize that increased AR expression in conjunction with

NIAID Data Ecosystem30

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

乳腺细胞分子机制

激素受体信号通路

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

ChEBI2012-07-30 更新20