首页/数据集/LATS1 and LATS2 suppress breast cancer progression by maintaining cell identity and metabolic state. LATS1 and LATS2 suppress breast cancer progression by maintaining cell identity and metabolic state

LATS1 and LATS2 suppress breast cancer progression by maintaining cell identity and metabolic state. LATS1 and LATS2 suppress breast cancer progression by maintaining cell identity and metabolic state

NIAID Data Ecosystem2026-03-10 收录

乳腺癌分子机制

LATS基因功能

数据链接：

https://www.ncbi.nlm.nih.gov/bioproject/PRJNA480288 数据链接链接失效反馈

官方服务：

资源简介：

This SuperSeries is composed of the SubSeries listed below. Overall design: Refer to individual Series

应用场景：

创建时间：

2018-07-09

乳腺癌分子机制

黄酮类化合物作用

Investigate differences in gene expresion profiles of T47-D human breast cancer cells when treated with baicalein. Gene expression profiling analysis from polyA RNA-seq of 2 replicates of T47-D cell

NIAID Data Ecosystem110

Additional file 1: of Inferring miRNA sponge co-regulation of protein-protein interactions in human breast cancer

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

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

Genome-wide Binding Site Mapping of Retinoic Acid Receptors and Coregulators in Breast Cancer Cells

乳腺癌分子机制

转录因子结合位点分析

Retinoic acid (RA) triggers growth-suppressive effects in tumor cells and therefore RA and its synthetic analogs have great potential as anti-carcinogenic agents. RA effects are mediated by retinoic a

NIAID Data Ecosystem100

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

LATS1 and LATS2 suppress breast cancer progression by maintaining cell identity and metabolic state. LATS1 and LATS2 suppress breast cancer progression by maintaining cell identity and metabolic state

资源简介：

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