26 results on '"Papillon-Cavanagh, Simon"'
Search Results
2. STK11 and KEAP1 mutations as prognostic biomarkers in an observational real-world lung adenocarcinoma cohort
3. Pan-cancer analysis of the effect of biopsy site on tumor mutational burden observations
4. The molecular landscape of ETMR at diagnosis and relapse
5. The histone mark H3K36me2 recruits DNMT3A and shapes the intergenic DNA methylation landscape
6. Histone H3K36 mutations promote sarcomagenesis through altered histone methylation landscape
7. H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis
8. Biomarker analysis from CheckMate 214: nivolumab plus ipilimumab versus sunitinib in renal cell carcinoma
9. Epigenetic dysregulation: a novel pathway of oncogenesis in pediatric brain tumors
10. A multi‐omic single cell sequencing approach to develop a CD8 T cell specific gene signature for anti‐PD1 response in solid tumors.
11. Mutation in The Nuclear-Encoded Mitochondrial Isoleucyl–tRNA Synthetase IARS2 in Patients with Cataracts, Growth Hormone Deficiency with Short Stature, Partial Sensorineural Deafness, and Peripheral Neuropathy or with Leigh Syndrome
12. Molecular correlates of response to nivolumab at baseline and on treatment in patients with RCC
13. Abstract 2008: Pan-cancer profiling of the effect of biopsied site on tumor mutational burden measurements in a real-world data cohort
14. Biomarker analyses from the phase III CheckMate 214 trial of nivolumab plus ipilimumab (N+I) or sunitinib (S) in advanced renal cell carcinoma (aRCC).
15. STK11 and KEAP1 Mutations as Prognostic Biomarkers in an Observational Real-World Lung Adenocarcinoma Cohort
16. Abstract 3221: T-cell receptor sequencing for pharmacodynamic and response biomarkers of checkpoint blockade
17. Abstract B44: Identification of epigenomic changes induced by H3 K27M mutation in glioblastoma using patient-derived and CRISPR/Cas9 edited cell lines
18. Abstract 08: Impaired H3K36 methylation defines a subset of head and neck squamous cell carcinomas
19. Spatial heterogeneity in medulloblastoma
20. Impaired H3K36 methylation defines a subset of head and neck squamous cell carcinomas
21. HG-76SPATIAL AND TEMPORAL HOMOGENEITY OF DRIVER MUTATIONS IN DIFFUSE INTRINSIC PONTINE GLIOMA
22. Spatial and temporal homogeneity of driver mutations in diffuse intrinsic pontine glioma
23. Mutation in The Nuclear-Encoded Mitochondrial Isoleucyl-tRNA SynthetaseIARS2in Patients with Cataracts, Growth Hormone Deficiency with Short Stature, Partial Sensorineural Deafness, and Peripheral Neuropathy or with Leigh Syndrome
24. Mutation in The Nuclear-Encoded Mitochondrial Isoleucyl-t RNA Synthetase IARS2 in Patients with Cataracts, Growth Hormone Deficiency with Short Stature, Partial Sensorineural Deafness, and Peripheral Neuropathy or with Leigh Syndrome.
25. Mutation in The Nuclear-Encoded Mitochondrial Isoleucyl-tRNA Synthetase IARS2 in Patients with Cataracts, Growth Hormone Deficiency with Short Stature, Partial Sensorineural Deafness, and Peripheral Neuropathy or with Leigh Syndrome.
26. Histone H3K36 mutations promote sarcomagenesis through altered histone methylation landscape.
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