239 results on '"Dorsch, Marion"'
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2. An ALK2 inhibitor, BLU-782, prevents heterotopic ossification in a mouse model of fibrodysplasia ossificans progressiva
3. A chemical biology screen identifies a vulnerability of neuroendocrine cancer cells to SQLE inhibition
4. Suppression of antitumor T cell immunity by the oncometabolite (R)-2-hydroxyglutarate
5. Data from AG-221, a First-in-Class Therapy Targeting Acute Myeloid Leukemia Harboring Oncogenic IDH2 Mutations
6. Supplementary Tables 1 - 8 from AG-221, a First-in-Class Therapy Targeting Acute Myeloid Leukemia Harboring Oncogenic IDH2 Mutations
7. Supplementary Figure 7 from Identification and Characterization of NVP-BKM120, an Orally Available Pan-Class I PI3-Kinase Inhibitor
8. Supplementary Figure 3 from Identification and Characterization of NVP-BKM120, an Orally Available Pan-Class I PI3-Kinase Inhibitor
9. Supplementary Figure 6 from Identification and Characterization of NVP-BKM120, an Orally Available Pan-Class I PI3-Kinase Inhibitor
10. Supplementary Methods from AG-221, a First-in-Class Therapy Targeting Acute Myeloid Leukemia Harboring Oncogenic IDH2 Mutations
11. Supplementary Figures 1 - 11 from AG-221, a First-in-Class Therapy Targeting Acute Myeloid Leukemia Harboring Oncogenic IDH2 Mutations
12. Supplementary Materials, Tables 1-2, Figure Legends 1-8 from Identification and Characterization of NVP-BKM120, an Orally Available Pan-Class I PI3-Kinase Inhibitor
13. Supplementary Figure 5 from Identification and Characterization of NVP-BKM120, an Orally Available Pan-Class I PI3-Kinase Inhibitor
14. Supplementary Figure 8 from Identification and Characterization of NVP-BKM120, an Orally Available Pan-Class I PI3-Kinase Inhibitor
15. Supplementary Figure 2 from Identification and Characterization of NVP-BKM120, an Orally Available Pan-Class I PI3-Kinase Inhibitor
16. Supplementary Figure 1 from Identification and Characterization of NVP-BKM120, an Orally Available Pan-Class I PI3-Kinase Inhibitor
17. Supplementary Figure 4 from Identification and Characterization of NVP-BKM120, an Orally Available Pan-Class I PI3-Kinase Inhibitor
18. Data from The Polycomb Group Protein Bmi-1 Is Essential for the Growth of Multiple Myeloma Cells
19. Supplementary Figure Legends 1-4 from PI3K Pathway Activation Mediates Resistance to MEK Inhibitors in KRAS Mutant Cancers
20. Supplementary Table 1 from The Polycomb Group Protein Bmi-1 Is Essential for the Growth of Multiple Myeloma Cells
21. Supplementary Figure Legends 1-13 from The Polycomb Group Protein Bmi-1 Is Essential for the Growth of Multiple Myeloma Cells
22. Supplemental Information from A Primary Xenograft Model of Small-Cell Lung Cancer Reveals Irreversible Changes in Gene Expression Imposed by Culture In vitro
23. Supplemental Tables A-H from A Primary Xenograft Model of Small-Cell Lung Cancer Reveals Irreversible Changes in Gene Expression Imposed by Culture In vitro
24. Data from A Primary Xenograft Model of Small-Cell Lung Cancer Reveals Irreversible Changes in Gene Expression Imposed by Culture In vitro
25. Supplementary Figures 1-4 from PI3K Pathway Activation Mediates Resistance to MEK Inhibitors in KRAS Mutant Cancers
26. Supplementary Methods from The Polycomb Group Protein Bmi-1 Is Essential for the Growth of Multiple Myeloma Cells
27. Supplementary Figures 1-13 from The Polycomb Group Protein Bmi-1 Is Essential for the Growth of Multiple Myeloma Cells
28. Increased Sensitivity to Apoptotic Stimuli in c-abl-deficient Progenitor B-Cell Lines
29. IDH2 mutation-induced histone and DNA hypermethylation is progressively reversed by small-molecule inhibition
30. ALDH2(E487K) mutation increases protein turnover and promotes murine hepatocarcinogenesis
31. PIM inhibitors target CD25-positive AML cells through concomitant suppression of STAT5 activation and degradation of MYC oncogene
32. A small molecule inhibitor of mutant IDH2 rescues cardiomyopathy in a D-2-hydroxyglutaric aciduria type II mouse model
33. Targeted Inhibition of Mutant IDH2 in Leukemia Cells Induces Cellular Differentiation
34. Evaluation of PRKACA as a Therapeutic Target for Fibrolamellar Carcinoma
35. Mechanisms of Rejection Induced by Tumor Cell-Targeted Gene Transfer of Interleukin 2, Interleukin 4, Interleukin 7, Tumor Necrosis Factor, or Interferon γ
36. Coordinate activation of Shh and PI3K signaling in PTEN-deficient glioblastoma: new therapeutic opportunities
37. Unraveling the therapeutic potential of the hedgehog pathway in cancer
38. Abstract 1262: BLU-701 is a highly potent, brain-penetrant and WT-sparing next-generation EGFR TKI for the treatment of sensitizing (ex19del, L858R) and C797S resistance mutations in metastatic NSCLC
39. Abstract 1467: BLU-945, a fourth-generation, potent and highly selective epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) with intracranial activity, demonstrates robust in vivo antitumor activity in models of osimertinib-resistant non-small cell lung cancer (NSCLC)
40. Abstract 1279: Development of a selective CDK2-E inhibitor in CCNE driven cancers
41. Abstract 1717: MAP4K1 inhibition enhances immune cell activation and anti-tumor immunity in preclinical tumor models
42. A crucial requirement for Hedgehog signaling in small cell lung cancer
43. Loss of the tumor suppressor Snf5 leads to aberrant activation of the Hedgehog-Gli pathway
44. Abstract A118: Identification of resistance mechanisms to FGFR4 targeted therapy in hepatocellular carcinoma
45. Abstract B127: Evaluating PRKACA as a therapeutic target for Fibrolamellar Carcinoma
46. Acquired On-Target Clinical Resistance Validates FGFR4 as a Driver of Hepatocellular Carcinoma
47. Validating cancer drug targets
48. Mechanisms of rejection induced by tumor cell-targeted gene transfer of interleukin 2, interleukin 4, interleukin 7, tumor necrosis factor, or interferon gamma
49. Tumor-Cell-Targeted Interleukin-7 Gene Transfer Reveals T-Cell-Dependent Antitumor Activity in vivo1
50. Ectopic expression of Delta4 impairs hematopoietic development and leads to lymphoproliferative disease
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