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2. A palmitate-rich metastatic niche enables metastasis growth via p65 acetylation resulting in pro-metastatic NF-κB signaling

4. Glutaredoxin 3 (GLRX3) confers a fusion oncogene-dependent vulnerability to Ewing sarcoma

5. Cooperation of cancer drivers with regulatory germline variants shapes clinical outcomes.

7. Small round cell sarcomas

8. Neomorphic DNA-binding enables tumor-specific therapeutic gene expression in fusion-addicted childhood sarcoma

9. Integrative gene network and functional analyses identify a prognostically relevant key regulator of metastasis in Ewing sarcoma

10. Somatic gene delivery for flexible in vivo modeling of high-risk sarcoma

12. Therapeutic targeting of the PLK1-PRC1-axis triggers cell death in genomically silent childhood cancer

13. Translational evidence for RRM2 as a prognostic biomarker and therapeutic target in Ewing sarcoma

20. Oncogenic hijacking of a developmental transcription factor evokes vulnerability toward oxidative stress in Ewing sarcoma

21. Publisher Correction: Oncogenic hijacking of a developmental transcription factor evokes vulnerability toward oxidative stress in Ewing sarcoma

22. Targeting the CALCB/RAMP1 axis inhibits growth of Ewing sarcoma

23. Ewing sarcoma

24. Chromosome 8 gain drives poor patient outcome via expression of 4E-BP1 in Ewing sarcoma

25. Systematic multi-omics cell line profiling uncovers principles of Ewing sarcoma fusion oncogene-mediated gene regulation

26. A palmitate-rich metastatic niche enables metastasis growth via p65 acetylation

27. Abstract PR004: Fusion protein-driven IGF-IR signals deregulate hippo pathway promoting oncogenic cooperation of YAP1 and FUS-DDIT3

28. Oncofusion-driven de novo enhancer assembly promotes malignancy in Ewing sarcoma via aberrant expression of the stereociliary protein LOXHD1

29. Additional file 3 of Neomorphic DNA-binding enables tumor-specific therapeutic gene expression in fusion-addicted childhood sarcoma

30. Additional file 1 of Neomorphic DNA-binding enables tumor-specific therapeutic gene expression in fusion-addicted childhood sarcoma

31. Chimeric EWSR1-FLI1 regulates the Ewing sarcoma susceptibility gene EGR2 via a GGAA microsatellite

32. Neomorphic DNA-binding enables tumor-specific therapeutic gene expression in fusion-addicted childhood sarcoma

33. Systematic multi-omics cell line profiling uncovers principles of Ewing sarcoma fusion oncogene-mediated gene regulation

34. Abstract 2003: Oncogenic interplay of FUS-DDIT3 and YAP1 in myxoid liposarcoma

35. Systematic multi-omics cell line profiling uncovers principles of Ewing sarcoma fusion oncogene-mediated gene regulation

36. Sarcoma treatment in the era of molecular medicine

37. Translational evidence for RRM2 as a prognostic biomarker and therapeutic target in Ewing sarcoma

38. Systems biology analysis identifies TCF7L1 as a key regulator of metastasis in Ewing sarcoma

39. Oncofusion-driven de novo enhancer assembly promotes malignancy in Ewing sarcoma via aberrant expression of the stereociliary protein LOXHD1

40. Sarcoma treatment in the era of molecular medicine

41. High Specificity of BCL11B and GLG1 for EWSR1-FLI1 and EWSR1-ERG Positive Ewing Sarcoma

42. Integrative clinical transcriptome analysis revealsTMPRSS2‐ERGdependency of prognostic biomarkers in prostate adenocarcinoma

43. Gene expression and immunohistochemical analyses identify SOX2 as major risk factor for overall survival and relapse in Ewing sarcoma patients

44. Oncogenic hijacking of a developmental transcription factor evokes therapeutic vulnerability for ROS-induction in Ewing sarcoma

45. Expression patterns of PD-L1 and PD-1 provide rationales for immune checkpoint inhibition in soft tissue sarcomas

46. Biomarker-based outcome prediction in prostate adenocarcinoma depends on theTMPRSS2-ERGstatus

47. Cooperation of dominant oncogenes with regulatory germline variants shapes clinical outcomes in childhood cancer

48. SOX2 expression identifies Ewing sarcoma patients with high risk for tumor relapse and poor survival

49. Targeting the CALCB/RAMP1-axis inhibits growth of Ewing sarcoma

50. Functional genomics identifies AMPD2 as a new prognostic marker for undifferentiated pleomorphic sarcoma

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