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1. Cytogenetic prognostication within medulloblastoma subgroups.

2. Subgroup-specific prognostic implications of TP53 mutation in medulloblastoma.

3. Second-generation molecular subgrouping of medulloblastoma: an international meta-analysis of Group 3 and Group 4 subtypes

4. Subgroup-specific structural variation across 1,000 medulloblastoma genomes.

6. Supplementary Data from Rapid Diagnosis of Medulloblastoma Molecular Subgroups

8. Medulloblastoma group 3 and 4 tumors comprise a clinically and biologically significant expression continuum reflecting human cerebellar development

9. MEDB-79. MYC-driven upregulation of thede novo serine and glycine pathway is a novel therapeutic target for Group 3 MYC-amplified Medulloblastoma

10. Divergent clonal selection dominates medulloblastoma at recurrence

12. Histologically defined central nervous system primitive neuro-ectodermal tumours (CNS-PNETs) display heterogeneous DNA methylation profiles and show relationships to other paediatric brain tumour types

14. Emergence and maintenance of actionable genetic drivers at medulloblastoma relapse

18. Advanced molecular pathology for rare tumours: A national feasibility study and model for centralised medulloblastoma diagnostics

19. MBRS-60. THE ACTIONABLE GENOMIC LANDSCAPE OF RELAPSED MEDULLOBLASTOMA IS DEFINED BY MAINTENANCE AND ACQUISITION OF DRIVER EVENTS

20. Time, pattern, and outcome of medulloblastoma relapse and their association with tumour biology at diagnosis and therapy: a multicentre cohort study

21. Abstract B73: Second-generation molecular subgrouping of medulloblastoma: An international meta-analysis of Group 3 and Group 4 subtypes

22. Subtypes of medulloblastoma have distinct developmental origins

23. Emergence and maintenance of actionable genetic drivers at medulloblastoma relapse.

28. MBCL-30. SUBGROUP-DIRECTED CLINICAL AND MOLECULAR STRATIFICATION OF DISEASE RISK IN INFANT MEDULLOBLASTOMA

29. Development of a targeted sequencing approach to identify prognostic, predictive and diagnostic markers in paediatric solid tumours

30. Divergent clonal selection dominates medulloblastoma at recurrence

31. MB-82THE TRANSCRIPTIONAL LANDSCAPE OF MEDULLOBLASTOMA: GROUP 3 AND GROUP 4 TUMOURS COMPRISE A SINGLE CLINICALLY SIGNIFICANT EXPRESSION CONTINUUM

32. Combined MYC and P53 Defects Emerge at Medulloblastoma Relapse and Define Rapidly Progressive, Therapeutically Targetable Disease

33. Combined MYC and P53 Defects Emerge at Medulloblastoma Relapse and Define Rapidly Progressive, Therapeutically Targetable Disease

34. Cytogenetic prognostication within medulloblastoma subgroups

38. TP53 Mutations in Favorable-Risk Wnt/Wingless-Subtype Medulloblastomas

41. Abstract 3448: Subtypes of medulloblastoma have distinct developmental origins

42. Rapid Diagnosis of Medulloblastoma Molecular Subgroups

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