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1. Heterogeneity within the PF-EPN-B ependymoma subgroup

2. DNA methylation-based classification of central nervous system tumours.

4. Spinal Myxopapillary Ependymomas Demonstrate a Warburg Phenotype

5. Molecular Classification of Ependymal Tumors across All CNS Compartments, Histopathological Grades, and Age Groups

6. Ependymoma

7. Genome Sequencing of SHH Medulloblastoma Predicts Genotype-Related Response to Smoothened Inhibition

8. Aberrant patterns of H3K4 and H3K27 histone lysine methylation occur across subgroups in medulloblastoma

9. MYCN amplification drives an aggressive form of spinal ependymoma

10. Clonal selection drives genetic divergence of metastatic medulloblastoma.

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

12. Ependymoma

13. Molecular heterogeneity and CXorf67 alterations in posterior fossa group A (PFA) ependymomas

14. A multi-institutional retrospective pooled outcome analysis of molecularly annotated pediatric supratentorial ZFTA-fused ependymoma

16. A multi-institutional retrospective pooled outcome analysis of molecularly annotated pediatric supratentorial ZFTA-fused ependymoma

17. Optimizing biomarkers for accurate ependymoma diagnosis, prognostication, and stratification within International Clinical Trials: A BIOMECA study.

18. Supplementary Table S1 from The Transcription Factor Evi-1 Is Overexpressed, Promotes Proliferation, and Is Prognostically Unfavorable in Infratentorial Ependymomas

19. Supplementary Figure 4 from Spinal Myxopapillary Ependymomas Demonstrate a Warburg Phenotype

20. Supplementary Data from Genetic Aberrations Leading to MAPK Pathway Activation Mediate Oncogene-Induced Senescence in Sporadic Pilocytic Astrocytomas

21. Supplementary Figure 2 from Spinal Myxopapillary Ependymomas Demonstrate a Warburg Phenotype

22. Supplementary Methods, Figure Legends 1-4 from Role of LIM and SH3 Protein 1 (LASP1) in the Metastatic Dissemination of Medulloblastoma

23. Supplementary Tables 1-6 from Role of LIM and SH3 Protein 1 (LASP1) in the Metastatic Dissemination of Medulloblastoma

24. Supplementary Figures 1-4 from Role of LIM and SH3 Protein 1 (LASP1) in the Metastatic Dissemination of Medulloblastoma

25. Data from Role of LIM and SH3 Protein 1 (LASP1) in the Metastatic Dissemination of Medulloblastoma

26. The current consensus on the clinical management of intracranial ependymoma and its distinct molecular variants

28. Optimising biomarkers for accurate ependymoma diagnosis, prognostication and stratification within International Clinical Trials: A BIOMECA study

29. The Impact of Different Visual Feedback Presentation Methods in a Wearable Computing Scenario

31. Hotspot Mutations in H3F3A and IDH1 Define Distinct Epigenetic and Biological Subgroups of Glioblastoma

32. An Animal Model of MYC-Driven Medulloblastoma

33. EPEN-24. Biological markers of ependymoma in children and adolescents (BIOMECA): Systematic comparison of methods for the precise evaluation of biomarkers for ependymoma diagnosis and prognostication

34. Delineation of Two Clinically and Molecularly Distinct Subgroups of Posterior Fossa Ependymoma

35. Papillary Tumor of the Pineal Region: A Distinct Molecular Entity

36. The landscape of genomic alterations across childhood cancers

37. Author Correction: The landscape of genomic alterations across childhood cancers

38. BCAT1 promotes cell proliferation through amino acid catabolism in gliomas carrying wild-type IDH1

40. Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomas

42. Ependymoma

43. Second series by the Italian Association of Pediatric Hematology and Oncology of children and adolescents with intracranial ependymoma: an integrated molecular and clinical characterization with a long-term follow-up

44. Biological and clinical heterogeneity of MYCN-amplified medulloblastoma

45. Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma

46. A novel human high-risk ependymoma stem cell model reveals the differentiation-inducing potential of the histone deacetylase inhibitor Vorinostat

47. Oncogenic FAM131B–BRAF fusion resulting from 7q34 deletion comprises an alternative mechanism of MAPK pathway activation in pilocytic astrocytoma

48. An activated mutant BRAF kinase domain is sufficient to induce pilocytic astrocytoma in mice

49. Focal genomic amplification at 19q13.42 comprises a powerful diagnostic marker for embryonal tumors with ependymoblastic rosettes

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