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Lunatic fringe deficiency cooperates with the Met/Caveolin amplicon to induce basal-like breast cancer
PubMed Full text in PMC Similar studies Analyze with GEO2R
Lunatic Fringe Deficiency Cooperates with the Met/Caveolin Gene Amplicon to Induce Basal-Like Breast Cancer
The effect of MFNG knockdown on gene expression profile of xenograft tumor derived from MDA-MB231 cells
Jagged1 regulates miRNA expression profile
Mammary Tissue: Wild type mammary glands vs IGF-IR induced mammary tumors vs IGF-IR independent tumors
Early parity-induced gene expression in total mammary epithelial cells and mammary cell subtypes in mice
Early parity-induced gene expression in total mammary epithelial cells in mice
Early parity-induced gene expression in mouse mammary cell subtypes
Met synergizes with p53 loss to induce mammary tumors that possess features of claudin-low breast cancer
Met synergizes with p53 loss to induce mammary tumors that possess features of claudin-low breast cancer (miRNA expression data).
Met synergizes with p53 loss to induce mammary tumors that possess features of claudin-low breast cancer (aCGH data).
Met synergizes with p53 loss to induce mammary tumors that possess features of claudin-low breast cancer (mRNA expression data).
Musashi proteins are post-transcriptional regulators of the epithelial-luminal cell state
PubMed Full text in PMC Similar studies SRA Run Selector
Expression data from freshly isolated mouse mammary luminal cells
Molecular Profiling of BRCA1-and BRCA2-associated Breast Cancers
aCGH analysis was performed in the spleen of βcat(ex3)osb mice
Effect of osteoblast-specific constitutive activation of beta-catenin or deletion of FoxO1 on gene expression in mice
Characterization of Cell Lines Derived from Breast Cancers and Normal Mammary Tissues for the Study of the Intrinsic Molecular Subtypes
Gene expression of primary MMTV-Neu tumors compared to secondary tumors generated from lin- and single tumor initiating cell (TIC) transplantation
Expression data from highly purified MMTV-Neu Tumor Initiating Cells (TICs) and the non-TIC CD24- fraction
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