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Expression of miR-200c in claudin-low breast cancer alters stem cell functionality, enhances chemosensitivity and reduces metastatic potential
PubMed Full text in PMC Similar studies Analyze with GEO2R
The miR-200b/200a/429 cluster prevents metastasis and induces dormancy in murine claudin-low mammary tumor cells
PubMed Full text in PMC Similar studies SRA Run Selector
Comparative oncogenomics identifies breast tumors enriched in functional tumor initiating cells
p53 regulates epithelial-mesenchymal transition (EMT) and stem cell properties through modulation of miRNAs.
miRNA expression profiling in human mammary epithelial cell (HMEC) CD24-CD44+ and non-CD24-CD44+ cell populations
The role of p53 in the regulation of miRNA expression profiling
HMLER cells expressing either FOXC2 or a vector control
SNAI1 overexpression effect on MCF-10A mammary epithelial cell line
SNAI1 overexpression effect on MCF-10A mammary epithelial cell line (miRNA)
SNAI1 overexpression effect on MCF-10A mammary epithelial cell line (mRNA)
Small RNA sequencing of extracellular vesicles from MDA-MB-231 cells treated with PBS, docetaxel (DTX), or doxorubicin (DOXO)
MDA-231EV, MDA-231c141 and MDA-231ba429 cells following injection of the cells into mammary glands of NCG and subsequent mammary tumor development
The effect of MFNG knockdown on gene expression profile of xenograft tumor derived from MDA-MB231 cells
Gene expression of SUM159 breast cancer cell line expressing microRNA--203
miR-203 overexpression effect on mesenchymal-like breast cancer cell line
PubMed Full text in PMC Similar studies GEO Profiles Analyze DataSet
Single-cell analysis reveals a stem cell program in human metastatic breast cancer cells
Single-cell analysis reveals a stem cell program in human metastatic breast cancer cells (Human patients - mammary cells)
Single-cell analysis reveals a stem cell program in human metastatic breast cancer cells (PDX mice - cancer cells)
Identification of enhancers in EMT and breast cancer stem cell formation
Identification of chromatin accessibility domains in EMT and breast cancer stem cell formation.
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