287 results on '"van Eijk, Ronald"'
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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. Incidence and determinants of thrombotic and bleeding complications in patients with glioblastoma
4. Cell-of-origin classification using the Hans and Lymph2Cx algorithms in primary cutaneous large B-cell lymphomas
5. External Quality Assessment on Molecular Tumor Profiling with Circulating Tumor DNA-Based Methodologies Routinely Used in Clinical Pathology within the COIN Consortium
6. Frequent mutated B2M, EZH2, IRF8, and TNFRSF14 in primary bone diffuse large B-cell lymphoma reflect a GCB phenotype
7. Molecular Background of Colorectal Tumors From Patients With Lynch Syndrome Associated With Germline Variants in PMS2
8. Detection of Circulating Tumor DNA for Disease Monitoring in Patients with Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type
9. Supplementary Table 1 from Enrichment of Low Penetrance Susceptibility Loci in a Dutch Familial Colorectal Cancer Cohort
10. Supplementary Table from Progression and Tumor Heterogeneity Analysis in Early Rectal Cancer
11. Supplementary Data from Cell Cycle/Apoptosis Molecule Expression Correlates with Imatinib Response in Patients with Advanced Gastrointestinal Stromal Tumors
12. Supplementary Table 1 from Genome-wide Allelic State Analysis on Flow-Sorted Tumor Fractions Provides an Accurate Measure of Chromosomal Aberrations
13. Supplementary Figure 1 from Genome-wide Allelic State Analysis on Flow-Sorted Tumor Fractions Provides an Accurate Measure of Chromosomal Aberrations
14. Data from Genome-wide Allelic State Analysis on Flow-Sorted Tumor Fractions Provides an Accurate Measure of Chromosomal Aberrations
15. Supplementary Figure 2 from Genome-wide Allelic State Analysis on Flow-Sorted Tumor Fractions Provides an Accurate Measure of Chromosomal Aberrations
16. Supplementary Figure and Table Legends from Genome-wide Allelic State Analysis on Flow-Sorted Tumor Fractions Provides an Accurate Measure of Chromosomal Aberrations
17. Supplementary Figure 3 from Genome-wide Allelic State Analysis on Flow-Sorted Tumor Fractions Provides an Accurate Measure of Chromosomal Aberrations
18. Supplementary Table 2 from Genome-wide Allelic State Analysis on Flow-Sorted Tumor Fractions Provides an Accurate Measure of Chromosomal Aberrations
19. Targeted DNA sequencing to identify genetic aberrations in glioblastoma that underlie venous thromboembolism; a cohort study
20. Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia
21. Molecular Diagnostics for TP53 Is Recommended in B-Cell Lymphomas
22. Polyostotic DLBCL Is Characterized By a NF-Κb Pathway Affecting Molecular Profile and Superior Survival
23. 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
24. A We–Centric Telecom Service for Police Officers to Support Communication
25. The clinical value of HER-2 overexpression and PIK3CA mutations in the older breast cancer population: a FOCUS study analysis
26. Federated Service Platform Solutions for Heterogeneous Wireless Networks
27. Assessment of a fully automated high-throughput DNA extraction method from formalin-fixed, paraffin-embedded tissue for KRAS, and BRAF somatic mutation analysis
28. Ubiquitous Attentiveness – Enabling Context-Aware Mobile Applications and Services
29. Improved risk assessment of endometrial cancer by combined analysis of MSI, PI3K–AKT, Wnt/β-catenin and P53 pathway activation
30. Handling heterogeneity in context aware services
31. Synchronous diffuse large B-cell lymphoma and mantle cell lymphoma: support for low-threshold biopsies and genetic testing
32. Clues for disease progression at time of diagnosis in patients with primary cutaneous follicle center lymphoma
33. Sensitive and Specific KRAS Somatic Mutation Analysis on Whole-Genome Amplified DNA from Archival Tissues
34. Erratum: Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia
35. 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
36. PIK3CA kinase domain mutation identifies a subgroup of stage III colon cancer patients with poor prognosis
37. Expression of HLA Class I Antigen, Aspirin Use, and Survival After a Diagnosis of Colon Cancer
38. Genome-wide copy neutral LOH is infrequent in familial and sporadic microsatellite unstable carcinomas
39. Synchronous diffuse large B-cell lymphoma and mantle cell lymphoma: support for low-threshold biopsies and genetic testing.
40. High-Resolution Analysis of Genomic Copy Number Changes
41. Genotyping and LOH Analysis on Archival Tissue using SNP Arrays
42. A We–Centric Telecom Service for Police Officers to Support Communication
43. Apparent Lack of BRAFV600E Derived HLA Class I Presented Neoantigens Hampers Neoplastic Cell Targeting by CD8+ T Cells in Langerhans Cell Histiocytosis
44. High Frequencies of Mutated EZH2 and IRF8 and Other Epigenetic Genes in Primary Bone Lymphomas Are Indicative of GCB-Phenotype
45. The complexity of screening PMS2 in DNA isolated from formalin-fixed paraffin-embedded material
46. Mass Spectrometry-Based Loss of Heterozygosity Analysis of Single-Nucleotide Polymorphism Loci in Paraffin Embedded Tumors Using the MassEXTEND Assay: Single-Nucleotide Polymorphism Loss of Heterozygosity Analysis of the Protein Tyrosine Phosphatase Receptor Type J in Familial Colorectal Cancer
47. Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura
48. High-resolution copy number analysis of paraffin-embedded archival tissue using SNP BeadArrays
49. Differential Gene Expression in Ovarian Tumors Reveals Dusp 4 and Serpina 5 As Key Regulators for Benign Behavior of Serous Borderline Tumors
50. Multiplex Ligation-Dependent Probe Amplification for the Detection of 1p and 19q Chromosomal Loss in Oligodendroglial Tumors
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