779 results on '"van Wezel, Tom"'
Search Results
2. Improving diagnostic accuracy of identifying gastric cancer patients with peritoneal metastases: tumor-guided cell-free DNA analysis of peritoneal fluid
3. Germline variant affecting p53β isoforms predisposes to familial cancer
4. Enrichment of colibactin-associated mutational signatures in unexplained colorectal polyposis patients
5. Real-world routine diagnostic molecular analysis for TP53 mutational status is recommended over p53 immunohistochemistry in B-cell lymphomas
6. Molecular and Clinicopathologic Characterization of Mismatch Repair-Deficient Endometrial Carcinoma Not Related to MLH1 Promoter Hypermethylation
7. Impact of genetic counseling strategy on diagnostic yield and workload for genome-sequencing-based tumor diagnostics
8. MLH1 Promotor Hypermethylation in Colorectal and Endometrial Carcinomas from Patients with Lynch Syndrome
9. Loss of bone morphogenetic protein signaling in fibroblasts results in CXCL12-driven serrated polyp development
10. Somatic hits in mismatch repair genes in colorectal cancer among non-seminoma testicular cancer survivors
11. Molecular Profile of MSH6-Associated Colorectal Carcinomas Shows Distinct Features From Other Lynch Syndrome–Associated Colorectal Carcinomas
12. Molecular functions of MCM8 and MCM9 and their associated pathologies
13. Clinicogenomic associations in childhood Langerhans cell histiocytosis: an international cohort study
14. The sensitivity of pan-TRK immunohistochemistry in solid tumours: A meta-analysis
15. Cell-of-origin classification using the Hans and Lymph2Cx algorithms in primary cutaneous large B-cell lymphomas
16. Statin use is associated with a reduced incidence of colorectal cancer expressing SMAD4
17. Author Correction: Mutational analysis of driver genes defines the colorectal adenoma: in situ carcinoma transition
18. Mutational analysis of driver genes defines the colorectal adenoma: in situ carcinoma transition
19. Use of sanger and next-generation sequencing to screen for mosaic and intronic APC variants in unexplained colorectal polyposis patients
20. Comedonecrosis Gleason pattern 5 is associated with worse clinical outcome in operated prostate cancer patients
21. Molecular analysis using SalvGlandDx improves risk of malignancy estimation and diagnosis of salivary gland cytopathology: An exploratory multicenter study
22. Frequent mutated B2M, EZH2, IRF8, and TNFRSF14 in primary bone diffuse large B-cell lymphoma reflect a GCB phenotype
23. The coding microsatellite mutation profile of PMS2-deficient colorectal cancer
24. The diverse molecular profiles of lynch syndrome-associated colorectal cancers are (highly) dependent on underlying germline mismatch repair mutations
25. RET Fluorescence In Situ Hybridization Analysis Is a Sensitive but Highly Unspecific Screening Method for RET Fusions in Lung Cancer
26. Cribriform architecture in radical prostatectomies predicts oncological outcome in Gleason score 8 prostate cancer patients
27. Clinicopathological characteristics of glomeruloid architecture in prostate cancer
28. Optimizing Mutation and Fusion Detection in NSCLC by Sequential DNA and RNA Sequencing
29. Comprehensive diagnostics of acute myeloid leukemia by whole transcriptome RNA sequencing
30. MLH1 Promotor Hypermethylation in Colorectal and Endometrial Carcinomas from Patients with Lynch Syndrome
31. BRAF V600E is associated with higher incidence of second cancers in adults with Langerhans cell histiocytosis
32. Impact of genetic counselling strategy on diagnostic yield and workload for genome sequencing-based tumour diagnostics
33. Robust detection of translocations in lymphoma FFPE samples using targeted locus capture-based sequencing
34. Declining detection rates for APC and biallelic MUTYH variants in polyposis patients, implications for DNA testing policy
35. HLA-G protein expression in colorectal cancer evaluated by immunohistochemistry and western blot analysis: Its expression characteristics remain enigmatic
36. Molecular Background of Colorectal Tumors From Patients With Lynch Syndrome Associated With Germline Variants in PMS2
37. Targeted next generation sequencing screening of Lynch syndrome in Tunisian population
38. Recommendations for the clinical interpretation and reporting of copy number gains using gene panel NGS analysis in routine diagnostics
39. Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13
40. Tumour-guided cell free tumour DNA analysis in peritoneal fluids of gastric cancer patients can detect occult peritoneal metastases
41. Use of CRISPR-modified human stem cell organoids to study the origin of mutational signatures in cancer
42. A clinically applicable molecular classification of oncocytic cell thyroid nodules
43. Molecular Profile of MSH6-Associated Colorectal Carcinomas Shows Distinct Features From Other Lynch Syndrome–Associated Colorectal Carcinomas
44. QPOLE: A Quick, Simple, and Cheap Alternative for POLE Sequencing in Endometrial Cancer by Multiplex Genotyping Quantitative Polymerase Chain Reaction
45. MLH1Promotor Hypermethylation in Colorectal and Endometrial Carcinomas from Patients with Lynch Syndrome
46. “The leading role of pathology in assessing the somatic molecular alterations of cancer: Position Paper of the European Society of Pathology”: letter to the Editor
47. Somatic POLE proofreading domain mutation, immune response, and prognosis in colorectal cancer: a retrospective, pooled biomarker study
48. SNP association study in PMS2-associated Lynch syndrome
49. RNA analysis of cancer predisposing genes in formalin-fixed paraffin-embedded tissue determines aberrant splicing
50. Excluding Lynch syndrome in a female patient with metachronous DNA mismatch repair deficient colon- and ovarian cancer
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