264 results on '"Ruano, Dina"'
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2. Real-world routine diagnostic molecular analysis for TP53 mutational status is recommended over p53 immunohistochemistry in B-cell lymphomas
3. γδ T cells are effectors of immunotherapy in cancers with HLA class I defects
4. Enrichment of colibactin-associated mutational signatures in unexplained colorectal polyposis patients
5. Cell-of-origin classification using the Hans and Lymph2Cx algorithms in primary cutaneous large B-cell lymphomas
6. Tumor-Infiltrating T Cells Can Be Expanded Successfully from Primary Uveal Melanoma after Separation from Their Tumor Environment
7. The Variable Genomic Landscape During Osteosarcoma Progression: Insights From a Longitudinal WGS Analysis.
8. Frequent mutated B2M, EZH2, IRF8, and TNFRSF14 in primary bone diffuse large B-cell lymphoma reflect a GCB phenotype
9. Optimizing Mutation and Fusion Detection in NSCLC by Sequential DNA and RNA Sequencing
10. Supplementary Table S2 from Neoantigen Targetability in Progressive Advanced Melanoma
11. Supplementary Methods S1 from Neoantigen Targetability in Progressive Advanced Melanoma
12. Supplementary Figure S3 from Neoantigen Targetability in Progressive Advanced Melanoma
13. Data from Neoantigen Targetability in Progressive Advanced Melanoma
14. Molecular Background of Colorectal Tumors From Patients With Lynch Syndrome Associated With Germline Variants in PMS2
15. Neoantigen Targetability in Progressive Advanced Melanoma
16. A clinically applicable molecular classification of oncocytic cell thyroid nodules
17. Revisiting immune escape in colorectal cancer in the era of immunotherapy
18. Supplemenatry figure 1 from Genomic Characterization of Vulvar (Pre)cancers Identifies Distinct Molecular Subtypes with Prognostic Significance
19. Figure S2 from Genomic Characterization of Vulvar (Pre)cancers Identifies Distinct Molecular Subtypes with Prognostic Significance
20. Table S1 from Genomic Characterization of Vulvar (Pre)cancers Identifies Distinct Molecular Subtypes with Prognostic Significance
21. Neoantigen-specific immunity in low mutation burden colorectal cancers of the consensus molecular subtype 4
22. CD103 and CD39 coexpression identifies neoantigen-specific cytotoxic T cells in colorectal cancers with low mutation burden
23. Targeted DNA sequencing to identify genetic aberrations in glioblastoma that underlie venous thromboembolism; a cohort study
24. Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia
25. Molecular Diagnostics for TP53 Is Recommended in B-Cell Lymphomas
26. Polyostotic DLBCL Is Characterized By a NF-Κb Pathway Affecting Molecular Profile and Superior Survival
27. Cancer-specific T helper shared and neo-epitopes uncovered by expression of the MHC class II master regulator CIITA
28. Genetic Stability of Driver Alterations in Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type and Their Relapses: A Rationale for the Use of Molecular-Based Methods for More Effective Disease Monitoring
29. A Paradoxical Role for Regulatory T Cells in the Tumor Microenvironment of Pancreatic Cancer
30. Local and systemic immune profiles of human pancreatic ductal adenocarcinoma revealed by single-cell mass cytometry
31. Targeting pancreatic cancer by TAK-981: a SUMOylation inhibitor that activates the immune system and blocks cancer cell cycle progression in a preclinical model
32. γδ T cells are effectors of immune checkpoint blockade in mismatch repair-deficient colon cancers with antigen presentation defects
33. Clues for disease progression at time of diagnosis in patients with primary cutaneous follicle center lymphoma
34. Yield and costs of molecular diagnostics on thyroid cytology slides in the Netherlands, adapting the Bethesda classification
35. Erratum: Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia
36. Whole-Exome Sequencing Studies of Parathyroid Carcinomas Reveal Novel PRUNE2 Mutations, Distinctive Mutational Spectra Related to APOBEC-Catalyzed DNA Mutagenesis and Mutational Enrichment in Kinases Associated With Cell Migration and Invasion
37. Prevalence and Prognosis of Lynch Syndrome and Sporadic Mismatch Repair Deficiency in Endometrial Cancer
38. Association of the gene encoding neurogranin with schizophrenia in males
39. Functional gene group analysis reveals a role of synaptic heterotrimeric G proteins in cognitive ability
40. Colorectal cancer risk variants on 11q23 and 15q13 are associated with unexplained adenomatous polyposis
41. Cancer-Specific T Helper Shared and Neo-Epitopes Uncovered by Expression of the MHC Class II Master Regulator CIITA
42. Transthyretin: No association between serum levels or gene variants and schizophrenia
43. The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: Evidence from a large collaborative study totaling 4,963 Subjects
44. Digenic inheritance ofMSH6andMUTYHvariants in familial colorectal cancer
45. The complexity of screening PMS2 in DNA isolated from formalin-fixed paraffin-embedded material
46. Identification of a neo-epitope dominating endogenous CD8 T cell responses to MC-38 colorectal cancer
47. MOESM7 of Neoantigen-specific immunity in low mutation burden colorectal cancers of the consensus molecular subtype 4
48. Molecular Diagnostics for TP53Is Recommended in B-Cell Lymphomas
49. Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia
50. Allelic Switching of DLX5, GRB10, and SVOPL during Colorectal Cancer Tumorigenesis
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