210 results on '"Tops, Bastiaan B J"'
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2. Correction to: Amplification of the PLAG-family genes—PLAGL1 and PLAGL2—is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification
3. Amplification of the PLAG-family genes—PLAGL1 and PLAGL2—is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification
4. GOPC:ROS1 and other ROS1 fusions represent a rare but recurrent drug target in a variety of glioma types
5. Mesenchymal tumor organoid models recapitulate rhabdomyosarcoma subtypes
6. PATZ1 fusions define a novel molecularly distinct neuroepithelial tumor entity with a broad histological spectrum
7. RT-PCR assay to detect FGFR3::TACC3 fusions in formalin-fixed, paraffin-embedded glioblastoma samples.
8. RT-PCR assay to detect FGFR3::TACC3 fusions in formalin-fixed, paraffin-embedded glioblastoma samples
9. Improved Gene Fusion Detection in Childhood Cancer Diagnostics Using RNA Sequencing
10. Recommendations for the clinical interpretation and reporting of copy number gains using gene panel NGS analysis in routine diagnostics
11. Molecular diagnostic tools for the World Health Organization (WHO) 2021 classification of gliomas, glioneuronal and neuronal tumors; an EANO guideline
12. RT-PCR assay to detect FGFR3::TACC3fusions in formalin-fixed, paraffin-embedded glioblastoma samples
13. Comprehensive routine diagnostic screening to identify predictive mutations, gene amplifications, and microsatellite instability in FFPE tumor material
14. Correction to: Amplification of the PLAG-family genes—PLAGL1 and PLAGL2—is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification (Acta Neuropathologica, (2023), 145, 1, (49-69), 10.1007/s00401-022-02516-2)
15. HER2, chromosome 17 polysomy and DNA ploidy status in breast cancer; a translational study
16. Additional file 1 of Systematic discovery of gene fusions in pediatric cancer by integrating RNA-seq and WGS
17. Amplification of the PLAG-family genes—PLAGL1 and PLAGL2—is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification
18. Molecular Characterization Reveals Subclasses of 1q Gain in Intermediate Risk Wilms Tumors
19. Significance of complete 1p/19q co-deletion, IDH1 mutation and MGMT promoter methylation in gliomas: use with caution
20. Implementation of paediatric precision oncology into clinical practice: The Individualized Therapies for Children with cancer program 'iTHER'
21. Mesenchymal tumor organoid models recapitulate rhabdomyosarcoma subtypes
22. Improved Gene Fusion Detection in Childhood Cancer Diagnostics Using RNA Sequencing
23. Mesenchymal tumor organoid models recapitulate rhabdomyosarcoma subtypes
24. Recurrent mutations in genes involved in nuclear factor-κB signalling in nodal marginal zone lymphoma—diagnostic and therapeutic implications
25. The homogeneous mutation status of a 22 gene panel justifies the use of serial sections of colorectal cancer tissue for external quality assessment
26. Identification of a novel MET mutation in high-grade glioma resulting in an auto-active intracellular protein
27. Author Reply to Peer Reviews of Mesenchymal tumor organoid models recapitulate rhabdomyosarcoma subtypes
28. Mesenchymal tumor organoid models recapitulate rhabdomyosarcoma subtypes
29. Immunoglobulin rearrangement analysis from multiple lesions in the same patient using next-generation sequencing
30. EWSR1—The Most Common Rearranged Gene in Soft Tissue Lesions, Which Also Occurs in Different Bone Lesions: An Updated Review
31. The end of the laboratory developed test as we know it?: Recommendations from a national multidisciplinary taskforce of laboratory specialists on the interpretation of the IVDR and its complications
32. NR4A3 rearrangement reliably distinguishes between the clinicopathologically overlapping entities myoepithelial carcinoma of soft tissue and cellular extraskeletal myxoid chondrosarcoma
33. Desmoid-type fibromatosis of the head and neck region in the paediatric population: a clinicopathological and genetic study of seven cases
34. Micro-costing diagnostics in oncology: from single-gene testing to whole- genome sequencing
35. Distribution of GOPC:ROS1 and other ROS1 fusions in glioma types
36. Additional file 1 of Comprehensive routine diagnostic screening to identify predictive mutations, gene amplifications, and microsatellite instability in FFPE tumor material
37. Additional file 3 of Comprehensive routine diagnostic screening to identify predictive mutations, gene amplifications, and microsatellite instability in FFPE tumor material
38. Comprehensive routine diagnostic screening to identify predictive mutations, gene amplifications, and microsatellite instability in FFPE tumor material
39. Presence of C11orf95–MKL2 fusion is a consistent finding in chondroid lipomas: a study of eight cases
40. A micrococcal nuclease homologue in RNAi effector complexes
41. RDE-2 interacts with MUT-7 to mediate RNA interference in Caenorhabditis elegans
42. Recommendations for the clinical interpretation and reporting of copy number gains using gene panel NGS analysis in routine diagnostics
43. Processing of primary microRNAs by the Microprocessor complex
44. Comprehensive molecular and clinicopathological analysis of vascular malformations: A study of 319 cases
45. The clinical implementation of copy number detection in the age of next-generation sequencing
46. Mutational analysis using Sanger and next generation sequencing in sporadic spindle cell hemangiomas: A study of 19 cases
47. RAS testing in metastatic colorectal cancer : Excellent reproducibility amongst 17 Dutch pathology centers
48. Recurrent mutations in genes involved in nuclear factor‐κB signalling in nodal marginal zone lymphoma—diagnostic and therapeutic implications
49. A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer
50. Immunoglobulin rearrangement analysis from multiple lesions in the same patient using next-generation sequencing
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