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Mapping the hallmarks of lung adenocarcinoma with massively parallel sequencing.
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Cell
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Frequent and focal FGFR1 amplification associates with therapeutically tractable FGFR1 dependency in squamous cell lung cancer.
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Sci Transl Med
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2010
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Integrative genome analyses identify key somatic driver mutations of small-cell lung cancer.
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Nat Genet
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4
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Predicting drug susceptibility of non-small cell lung cancers based on genetic lesions.
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J Clin Invest
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2009
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Mutations in the DDR2 kinase gene identify a novel therapeutic target in squamous cell lung cancer.
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J Clin Oncol
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9
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New non-viral method for gene transfer into primary cells.
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Vandetanib plus pemetrexed for the second-line treatment of advanced non-small-cell lung cancer: a randomized, double-blind phase III trial.
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Early palliative care for patients with advanced cancer: how to make it work?
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14
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Transforming growth factor beta inhibition increases mortality and left ventricular dilatation after myocardial infarction.
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Basic Res Cardiol
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1.52
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15
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Definition of a fluorescence in-situ hybridization score identifies high- and low-level FGFR1 amplification types in squamous cell lung cancer.
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Mod Pathol
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1.50
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16
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Determinants and patient-reported long-term outcomes of physician empathy in oncology: a structural equation modelling approach.
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1.46
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17
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Tumor VEGF:VEGFR2 autocrine feed-forward loop triggers angiogenesis in lung cancer.
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18
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Hodgkin's lymphoma cell lines are characterized by frequent aberrations on chromosomes 2p and 9p including REL and JAK2.
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19
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Cancer Discov
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2014
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20
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Cell-autonomous and non-cell-autonomous mechanisms of transformation by amplified FGFR1 in lung cancer.
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Cancer Discov
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2013
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21
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Early detection of erlotinib treatment response in NSCLC by 3'-deoxy-3'-[F]-fluoro-L-thymidine ([F]FLT) positron emission tomography (PET).
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PLoS One
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22
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Clin Cancer Res
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Expression of signaling mediators downstream of EGF-receptor predict sensitivity to small molecule inhibitors directed against the EGF-receptor pathway.
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Quantitative analysis of response to treatment with erlotinib in advanced non-small cell lung cancer using 18F-FDG and 3'-deoxy-3'-18F-fluorothymidine PET.
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J Nucl Med
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25
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Clinical pharmacokinetics of tyrosine kinase inhibitors: focus on pyrimidines, pyridines and pyrroles.
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Clin Pharmacokinet
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1.08
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26
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Predictive value of early and late residual 18F-fluorodeoxyglucose and 18F-fluorothymidine uptake using different SUV measurements in patients with non-small-cell lung cancer treated with erlotinib.
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Eur J Nucl Med Mol Imaging
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Left ventricular remodeling after myocardial infarction in mice with targeted deletion of the NADPH oxidase subunit gp91PHOX.
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Basic Res Cardiol
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28
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Identification of novel fusion genes in lung cancer using breakpoint assembly of transcriptome sequencing data.
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Genome Biol
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Part I: Hodgkin's lymphoma--molecular biology of Hodgkin and Reed-Sternberg cells.
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Lancet Oncol
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Clinical pharmacokinetics of tyrosine kinase inhibitors: focus on 4-anilinoquinazolines.
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Constitutive expression of c-FLIP in Hodgkin and Reed-Sternberg cells.
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Diarrhea associated with afatinib: an oral ErbB family blocker.
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Downregulation of 18F-FDG uptake in PET as an early pharmacodynamic effect in treatment of non-small cell lung cancer with the mTOR inhibitor everolimus.
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The endocannabinoid arachidonyl ethanolamide (anandamide) increases pulmonary arterial pressure via cyclooxygenase-2 products in isolated rabbit lungs.
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Identification of lung cancer with high sensitivity and specificity by blood testing.
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CASPAR: a hierarchical bayesian approach to predict survival times in cancer from gene expression data.
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Spatial Tumor Heterogeneity in Lung Cancer with Acquired Epidermal Growth Factor Receptor-Tyrosine Kinase Inhibitor Resistance: Targeting High-Level MET-Amplification and EGFR T790M Mutation Occurring at Different Sites in the Same Patient.
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Modeling tumor dynamics and overall survival in advanced non-small-cell lung cancer treated with erlotinib.
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Validation of the "SmoCess-GP" instrument - a short patient questionnaire for assessing the smoking cessation activities of general practitioners: a cross-sectional study.
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Monitoring reversible and irreversible EGFR inhibition with erlotinib and afatinib in a patient with EGFR-mutated non-small cell lung cancer (NSCLC) using sequential [18F]fluorothymidine (FLT-)PET.
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