33 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. Recurrent somatic mutations in ACVR1 in pediatric midline high-grade astrocytoma.
6. The histone mark H3K36me2 recruits DNMT3A and shapes the intergenic DNA methylation landscape
7. Histone H3K36 mutations promote sarcomagenesis through altered histone methylation landscape
8. H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis
9. Biomarker analysis from CheckMate 214: nivolumab plus ipilimumab versus sunitinib in renal cell carcinoma
10. Epigenetic dysregulation: a novel pathway of oncogenesis in pediatric brain tumors
11. A multi‐omic single cell sequencing approach to develop a CD8 T cell specific gene signature for anti‐PD1 response in solid tumors.
12. 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
13. Molecular correlates of response to nivolumab at baseline and on treatment in patients with RCC
14. mRMRe: an R package for parallelized mRMR ensemble feature selection
15. Comparison and validation of genomic predictors for anticancer drug sensitivity
16. Abstract 2008: Pan-cancer profiling of the effect of biopsied site on tumor mutational burden measurements in a real-world data cohort
17. Biomarker analyses from the phase III CheckMate 214 trial of nivolumab plus ipilimumab (N+I) or sunitinib (S) in advanced renal cell carcinoma (aRCC).
18. STK11 and KEAP1 Mutations as Prognostic Biomarkers in an Observational Real-World Lung Adenocarcinoma Cohort
19. Abstract 3221: T-cell receptor sequencing for pharmacodynamic and response biomarkers of checkpoint blockade
20. Abstract B44: Identification of epigenomic changes induced by H3 K27M mutation in glioblastoma using patient-derived and CRISPR/Cas9 edited cell lines
21. Abstract 08: Impaired H3K36 methylation defines a subset of head and neck squamous cell carcinomas
22. Spatial heterogeneity in medulloblastoma
23. Impaired H3K36 methylation defines a subset of head and neck squamous cell carcinomas
24. HG-76SPATIAL AND TEMPORAL HOMOGENEITY OF DRIVER MUTATIONS IN DIFFUSE INTRINSIC PONTINE GLIOMA
25. Spatial and temporal homogeneity of driver mutations in diffuse intrinsic pontine glioma
26. 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
27. Fusion of TTYH1 with the C19MC microRNA cluster drives expression of a brain-specific DNMT3B isoform in the embryonal brain tumor ETMR
28. Mutations in C5ORF42 Cause Joubert Syndrome in the French Canadian Population
29. 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.
30. Fusion of TTYH1 with the C19MC microRNA cluster drives expression of a brain-specific DNMT3B isoform in the embryonal brain tumor ETMR.
31. 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.
32. Histone H3K36 mutations promote sarcomagenesis through altered histone methylation landscape.
33. Mutations in a novel serine protease PRSS56 in families with nanophthalmos.
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