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The microRNAs with potential in predicting lung metastasis of triple negative breast cancer
PubMed Full text in PMC Similar studies Analyze with GEO2R
MicroRNA expression data from an epithelial-mesenchymal transition (EMT) model of triple negative breast cancer (TNBC).
Deregulated microRNAs in triple-negative breast cancer revealed by deep sequencing
PubMed Full text in PMC Similar studies SRA Run Selector
Genome-wide analysis of gene expression patterns in human kidney cancer
Genome-wide analysis of gene expression patterns in human kidney cancer [patients with metastasis]
Genome-wide analysis of gene expression patterns in human kidney cancer [patients without metastasis]
Differentially expressed genes after miRNA or siRNA transfection in human cancer cell lines (III)
Differentially expressed genes after miRNA or siRNA transfection in human cancer cell lines II
Gene Expression data from SH3GL2 overexpressing SUM-159 cells
Differential miRNA expression profiles of primary and relapse lesions of breast cancer patients receiving tamoxifen
Encapsulated miR-200c and Nkx2.1 in a nuclear/mitochondria transcriptional regulatory network of non-metastatic and metastatic lung cancer cells
p53 deficiency linked to BTG2 loss enhances metastatic potential by promoting tumor growth in primary and metastatic sites in PDX models of triple negative breast cancer
PubMed Full text in PMC Similar studies Analyze with GEO2RSRA Run Selector
High-throughput RNA sequencing on circular RNA profiles of human triple-negative breast cancer and adjacent normal tissues
circRNA expression in breast cancer
circRNA expression in breast cancer and non-tumor breast tissues
circRNA expression in breast cancer cell lines
RNA sequencing in LLCs from co-injected mice or LLC injection alone.
Murine cells: MSC+LLC-serum-exosome vs LLC-serum-exosome
Murine MSCs: MSC-exosome-hypoxia vs MSC-exosome-normoxia
A microRNA signature identifies four subtypes of triple-negative breast cancer and correlates miR-342-3p as a regulator of the lactate metabolic pathway through silencing the monocarboxylate transporter 1
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