18 results on '"Peng R"'
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2. MA17.08 Whole-Genome CRISPR Screening Reveals Genetic Vulnerabilities and Therapeutic Targets in Malignant Pleural Mesothelioma
3. P2.21-08 Mutant NF2-Driven De Novo Pyrimidine Synthesis is a Metabolic Vulnerability in Malignant Pleural Mesothelioma
4. P2.21-09 Single-Cell Dissection Reveals Mesothelial Heterogeneity and Dysfunctional Immunity in Malignant Pleural Mesothelioma
5. P2.14A.09 Adaptive Reprogramming of Arginine Biosynthesis is an Attractive Target for Modulating the Response to WEE1 Inhibition in Pleural Mesothelioma
6. Characterization of tumor infiltrating lymphocytes in resectable early stage non-small cell lung cancer: 98O
7. Prolonged pemetrexed pretreatment increases efficiency of ionizing radiation combination therapy and correlates with the persistence of treatment-induced DNA damage in lung cancer cells: 23P
8. Increased schedule-dependent efficiency of pemetrexed–cisplatin combination therapy eliminates resistant lung cancer stem-like cells associated with EMT: 22P
9. Epithelial-to-mesenchymal transition (EMT) is required for resistance to anti-folate chemotherapy in lung cancer: 18P
10. P71.03 A New Combination Therapy for FGFR1-Amplified Lung Cancer
11. 19P A synergistic combination therapy for KRAS-driven cancers
12. MA06.05 Targeting Anti-Apoptotic Mechanisms in Malignant Pleural Mesothelioma
13. P73.03 A Kinome CRISPR Screen in FGFR-Amplified Lung Cancer
14. P62.07 Investigation of Metabolic Vulnerabilities Specific to STK11-mutant Lung Cancer
15. 18P Epithelial-to-mesenchymal transition (EMT) is required for resistance to anti-folate chemotherapy in lung cancer
16. 98O: Characterization of tumor infiltrating lymphocytes in resectable early stage non-small cell lung cancer
17. 23P Prolonged pemetrexed pretreatment increases efficiency of ionizing radiation combination therapy and correlates with the persistence of treatment-induced DNA damage in lung cancer cells
18. 22P Increased schedule-dependent efficiency of pemetrexed–cisplatin combination therapy eliminates resistant lung cancer stem-like cells associated with EMT
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