Metastatic site influences driver gene function in pancreatic cancer
收藏NIAID Data Ecosystem2026-05-02 收录
官方服务：
资源简介：
This SuperSeries is composed of the SubSeries listed below. Refer to individual Series
应用场景：
创建时间：
2025-06-14
相关数据集
NFIC1 suppresses migration and invasion of breast cancer cells through interferon-mediated Jak-STAT pathway
NFIC1, the longest isoform of NFIC, is essential for the regulation on spatiotemporal expressions of drug-metabolizing genes in liver. However, the role of NFIC1 in breast cancer is not clear. Here we
NIAID Data Ecosystem40
Additional file 2 of An integrated multi-omics approach to identify regulatory mechanisms in cancer metastatic processes
Additional file 2. Gene set characterization. Gene set characterization of the DE genes between early and late stages. The downregulated genes are significantly enriched for cancer-related gene signat
NIAID Data Ecosystem30
Gene expression profiling of control and Carmil3-deficient 4T1 cells. Gene expression profiling of control and Carmil3-deficient 4T1 cells
To systemically study the molecular function of CARMIL3 in cancer cells, we used mammary tumor cells, 4T1, as a model and genetically depleted Carmil3 via CRISPR/Cas9 strategy, followed by genome-wide
NIAID Data Ecosystem10
Flag-RBM47 HITS-CLIP in brain metastatic derivatives of MDA-MB-231
Brain metastatic breast cancer cells were subjected to HITS-CLIP to identify the targets of the RNA binding protein RBM47 MDA231-BrM2a is characterized in PMID: 19421193; Related data published toget
NIAID Data Ecosystem40
shRNAi profiling of human MDA-MB-231 cells expressing anti-p53 (shp53) short-hairpin RNAs treated with TFGbeta or control
TGFβ ligands act as tumor suppressors in early stage tumors but are paradoxically diverted into potent prometastatic factors in advanced cancers. The molecular nature of this switch remains enigmatic.
NIAID Data Ecosystem30
