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Identification of miRNA targets in breast cancer cells (DICER1 and DROSHA knockdown)

ChEBI2013-10-21 更新2026-07-21 收录

miRNA靶标识别

乳腺癌分子机制

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-48160 数据链接链接失效反馈

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资源简介：

Identification of miRNA targets in breast cancer cells (DICER1 and DROSHA knockdown)

应用场景：

创建时间：

2013-10-21

乳腺癌分子机制

RNA调控网络

BRCA-related miRNA sponge interaction network. The network includes 37076 miRNA sponge interactions. (XLSX 484Â kb)

NIAID Data Ecosystem70

The primer sequence.

乳腺癌分子机制

癌症药物靶点

BackgroundBreast cancer continues to be a predominant cause of female mortality globally, characterized by limited therapeutic options and substantial adverse effects. Artesunate (ART), a traditional

Figshare2025-08-04 更新40

Supplementary Table S4 from SMARCA4 Inhibits Breast Cancer Progression and Metastasis through RHOA Suppression

乳腺癌分子机制

肿瘤转移抑制

Supplementary Table S4

Figshare2025-05-15 更新30

Shc proteins in DMBA induced breast cancer

乳腺癌分子机制

基因编辑模型

The principal factors that control mammary tumor formation remain insufficiently defined. Shc adaptor proteins play an important role in signaling by three well-established biological markers for prog

NIAID Data Ecosystem70

Dietary ligands diindolylmethane and resveratrol result in diverse ERα signaling not seen after E2 and a subset of diindolylmethane mediated signaling needs concurrent AHR activation.. Dietary ligands diindolylmethane and resveratrol result in diverse ERα signaling not seen after E2 and a subset of diindolylmethane mediated signaling needs concurrent AHR activation.

乳腺癌分子机制

受体信号通路

Inhibitory crosstalk between estrogen receptor alpha (ER alpha ) and aryl hydrocarbon receptor (AHR) regulates 17-estradiol (E2)-dependent breast cancer cell signaling. ER alpha and AHR are transcript

NIAID Data Ecosystem40

Identification of miRNA targets in breast cancer cells (DICER1 and DROSHA knockdown)

资源简介：

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