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2. Reversible transitions between noradrenergic and mesenchymal tumor identities define cell plasticity in neuroblastoma

4. Senescence Induced by BMI1 Inhibition Is a Therapeutic Vulnerability in H3K27M-Mutant DIPG

5. Reciprocal H3.3 gene editing identifies K27M and G34R mechanisms in pediatric glioma including NOTCH signaling.

6. Low Bcl-2 is a robust biomarker of sensitivity to nab-paclitaxel in Ewing sarcoma

7. SPARC-mediated long-term retention of nab-paclitaxel in pediatric sarcomas

8. PPM1D mutations are oncogenic drivers of de novo diffuse midline glioma formation

9. MIF/CXCR4 signaling axis contributes to survival, invasion, and drug resistance of metastatic neuroblastoma cells in the bone marrow microenvironment

10. Targeting GPC2 on intraocular and CNS metastatic retinoblastomas with local and systemic delivery of CAR T-cells

12. Novel and shared neoantigen derived from histone 3 variant H3.3K27M mutation for glioma T cell therapy

13. Selective inhibition of HDAC6 regulates expression of the oncogenic driver EWSR1-FLI1 through the EWSR1 promoter in Ewing sarcoma

14. Treatment-driven selection of chemoresistant Ewing sarcoma tumors with limited drug distribution

15. LIN28B Underlies the Pathogenesis of a Subclass of Ewing Sarcoma

16. A high-risk retinoblastoma subtype with stemness features, dedifferentiated cone states and neuronal/ganglion cell gene expression

17. Developmental and oncogenic programs in H3K27M gliomas dissected by single-cell RNA-seq

20. Epigenetic loss of RNA-methyltransferase NSUN5 in glioma targets ribosomes to drive a stress adaptive translational program

23. Immunohistochemical expression of TFF1 is a marker of poor prognosis in retinoblastoma

26. Targeted drug distribution in tumor extracellular fluid of GD2-expressing neuroblastoma patient-derived xenografts using SN-38-loaded nanoparticles conjugated to the monoclonal antibody 3F8

31. Functional diversity and cooperativity between subclonal populations of pediatric glioblastoma and diffuse intrinsic pontine glioma cells

32. Immunohistochemical expression of TFF1 is a new prognostic marker in retinoblastoma

34. DIPG-19. BAF COMPLEX PERTURBATION AS A NOVEL THERAPEUTIC OPPORTUNITY IN H3K27M PEDIATRIC GLIOMA

35. Preclinical platform of retinoblastoma xenografts recapitulating human disease and molecular markers of dissemination

38. ALPL-1 is a target for chimeric antigen receptor therapy in osteosarcoma

39. Supplementary information. ALPL-1 is a target for chimeric antigen receptor therapy in osteosarcoma

40. Low Bcl-2 is a robust biomarker of sensitivity to nab-paclitaxel in Ewing sarcoma

41. Reversible transitions between noradrenergic and mesenchymal tumor identities define cell plasticity in neuroblastoma

42. Combination Therapies Targeting ALK-aberrant Neuroblastoma in Preclinical Models

43. Immunohistochemical expression of TFF1 is a marker of poor prognosis in retinoblastoma.

44. Therapeutic targeting of ependymoma as informed by oncogenic enhancer profiling

45. Data from BAF Complex Maintains Glioma Stem Cells in Pediatric H3K27M Glioma

46. Supplementary Table from BAF Complex Maintains Glioma Stem Cells in Pediatric H3K27M Glioma

48. Supplementary Figure from BAF Complex Maintains Glioma Stem Cells in Pediatric H3K27M Glioma

49. Data from Combination Therapies Targeting ALK-aberrant Neuroblastoma in Preclinical Models

50. Figure S2 from Combination Therapies Targeting ALK-aberrant Neuroblastoma in Preclinical Models

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