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Gene Expression Patterns that Predict Sensitivity to Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Lung Cancer Cell Lines and Human Lung Tumors
PubMed Full text in PMC Similar studies Analyze with GEO2R
Clinical Utility of Patient Derived Xenografts to Determine Biomarkers of Prognosis and Map Resistance Pathways in EGFR-Mutant Lung Adenocarcinoma
PubMed Similar studies Analyze with GEO2R
Gefitinib sensitivity in NSCLC cell lines
Gefitinib effect on various non-small cell lung cancer cell lines (HG-U133B)
PubMed Full text in PMC Similar studies GEO Profiles Analyze DataSet
Gefitinib effect on various non-small cell lung cancer cell lines (HG-U133A)
Expression data from EGFR mutant transgenic mice
An epithelial-mesenchymal transition (EMT) gene signature predicts resistance to erlotinib and PI3K pathway inhibitors and identifies Axl as a novel EMT marker in non-small cell lung cancer.
Expression profiling of lung cancer cell lines (UTSW Lung Panel V2)
Expression profiling of lung cancer cell lines
Gene expression-signatures for non-small cell lung cancer patients with different EGFR muational status.
Microarray expression profile of long noncoding RNAs in EGFR-TKI resistance of lung adenocarcinoma
Gene Expression Regulation by Lung Cancer Oncogenes
Axl mediates acquired resistance of head and neck cancer cells to the epidermal growth factor receptor inhibitor erlotinib
Genomic CpG methylation and TKI-response of the patient with advanced stage lung adenocarcinoma
PubMed Full text in PMC Similar studies
Gene expression data for pathological stage I-II lung adenocarcinomas
Expression data from the subclones of Lewis Lung Carcinoma (LLC) cells
Translational application of pharmacogenomics for refractory lung cancer
PubMed Full text in PMC Similar studies Analyze with GEO2RSRA Run Selector
Gene profiling, mutations and expression of epidermal growth factor receptor in androgen-dependent prostate cancer
Analysis of ETS gene expression patterns uncovers novel ETS mediated gene silencing pathways in prostate cancers
Coordinated over-expression of genes in the EGFR pathway predicts sensitivity to EGFR inhibition in pancreatic cancer
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