510 results on '"van Wezel, Tom"'
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2. Enrichment of colibactin-associated mutational signatures in unexplained colorectal polyposis patients
3. Assessing pathogenicity of mismatch repair variants of uncertain significance by molecular tumor analysis
4. Molecular Profile of MSH6-Associated Colorectal Carcinomas Shows Distinct Features From Other Lynch Syndrome–Associated Colorectal Carcinomas
5. Molecular functions of MCM8 and MCM9 and their associated pathologies
6. Somatic hits in mismatch repair genes in colorectal cancer among non-seminoma testicular cancer survivors
7. Clinicogenomic associations in childhood Langerhans cell histiocytosis: an international cohort study
8. Author Correction: Mutational analysis of driver genes defines the colorectal adenoma: in situ carcinoma transition
9. Mutational analysis of driver genes defines the colorectal adenoma: in situ carcinoma transition
10. Statin use is associated with a reduced incidence of colorectal cancer expressing SMAD4
11. Comedonecrosis Gleason pattern 5 is associated with worse clinical outcome in operated prostate cancer patients
12. Frequent mutated B2M, EZH2, IRF8, and TNFRSF14 in primary bone diffuse large B-cell lymphoma reflect a GCB phenotype
13. The diverse molecular profiles of lynch syndrome-associated colorectal cancers are (highly) dependent on underlying germline mismatch repair mutations
14. RET Fluorescence In Situ Hybridization Analysis Is a Sensitive but Highly Unspecific Screening Method for RET Fusions in Lung Cancer
15. Cribriform architecture in radical prostatectomies predicts oncological outcome in Gleason score 8 prostate cancer patients
16. Molecular and Clinicopathologic Characterization of Mismatch Repair-Deficient Endometrial Carcinoma Not Related to MLH1 Promoter Hypermethylation
17. Clinicopathological characteristics of glomeruloid architecture in prostate cancer
18. Optimizing Mutation and Fusion Detection in NSCLC by Sequential DNA and RNA Sequencing
19. Robust detection of translocations in lymphoma FFPE samples using targeted locus capture-based sequencing
20. Declining detection rates for APC and biallelic MUTYH variants in polyposis patients, implications for DNA testing policy
21. BRAF V600E is associated with higher incidence of second cancers in adults with Langerhans cell histiocytosis
22. Impact of genetic counselling strategy on diagnostic yield and workload for genome sequencing-based tumour diagnostics
23. Molecular Background of Colorectal Tumors From Patients With Lynch Syndrome Associated With Germline Variants in PMS2
24. Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13
25. Molecular Profile of MSH6-Associated Colorectal Carcinomas Shows Distinct Features From Other Lynch Syndrome–Associated Colorectal Carcinomas
26. Recurrent ETV3::NCOA2 fusions and MAPK pathway mutations in indeterminate dendritic cell histiocytosis
27. RNA analysis of cancer predisposing genes in formalin-fixed paraffin-embedded tissue determines aberrant splicing
28. QPOLE: A Quick, Simple, and Cheap Alternative for POLE Sequencing in Endometrial Cancer by Multiplex Genotyping Quantitative Polymerase Chain Reaction
29. Loss of bone morphogenetic protein signaling in fibroblasts results in CXCL12-driven serrated polyp development
30. Clinicogenomic associations in childhood Langerhans cell histiocytosis:an international cohort study
31. QPOLE:A Quick, Simple, and Cheap Alternative for POLE Sequencing in Endometrial Cancer by Multiplex Genotyping Quantitative Polymerase Chain Reaction
32. Molecular Profile of MSH6-Associated Colorectal Carcinomas Shows Distinct Features From Other Lynch Syndrome–Associated Colorectal Carcinomas
33. Differentiating Benign from Malignant Thyroid Tumors by Kinase Activity Profiling and Dabrafenib BRAF V600E Targeting.
34. Formalin-fixed, paraffin-embedded (FFPE) tissue epigenomics using Infinium HumanMethylation450 BeadChip assays
35. Specific (sialyl-)Lewis core 2 O-glycans differentiate colorectal cancer from healthy colon epithelium
36. Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia
37. Functional Analysis Identifies Damaging CHEK2 Missense Variants Associated with Increased Cancer Risk
38. Molecular Diagnostics for TP53 Is Recommended in B-Cell Lymphomas
39. Polyostotic DLBCL Is Characterized By a NF-Κb Pathway Affecting Molecular Profile and Superior Survival
40. 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
41. BRAFV600E is associated with higher incidence of second cancers in adults with Langerhans cell histiocytosis
42. BRAFV600Eis associated with higher incidence of second cancers in adults with Langerhans cell histiocytosis
43. Specific (sialyl-)Lewis core 2 O-glycans differentiate colorectal cancer from healthy colon epithelium
44. Germline MBD4 deficiency causes a multi-tumor predisposition syndrome
45. Functional Analysis Identifies Damaging CHEK2 Missense Variants Associated with Increased Cancer Risk
46. Everolimus in Patients With Advanced Follicular-Derived Thyroid Cancer: Results of a Phase II Clinical Trial
47. Germline MBD4 deficiency causes a multi-tumor predisposition syndrome
48. Downregulation of CASR expression and global loss of parafibromin staining are strong negative determinants of prognosis in parathyroid carcinoma
49. Comprehensive Molecular Analysis of Inflammatory Myofibroblastic Tumors Reveals Diverse Genomic Landscape and Potential Predictive Markers for Response to Crizotinib
50. Real-World Approach for Molecular Analysis of Acquired EGFR Tyrosine Kinase Inhibitor Resistance Mechanisms in NSCLC
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