612 results on '"Rosty, Christophe"'
Search Results
2. Inherited BRCA1 and RNF43 pathogenic variants in a familial colorectal cancer type X family
3. A mosaic pathogenic variant in MSH6 causes MSH6-deficient colorectal and endometrial cancer in a patient classified as suspected Lynch syndrome: a case report
4. A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
5. Recommendations for standardizing biopsy acquisition and histological assessment of immune checkpoint inhibitor-associated colitis
6. Pathology of Gastrointestinal Polyposis Disorders
7. Colorectal endometriosis – a challenging, often overlooked cause of colorectal pathology: a clinicopathological review of 114 cases
8. Rare germline variants in the AXIN2 gene in families with colonic polyposis and colorectal cancer
9. Identifying colorectal cancer caused by biallelic MUTYH pathogenic variants using tumor mutational signatures
10. Body Mass Index, sex, non-steroidal anti-inflammatory drug medications, smoking and alcohol are differentially associated with World Health Organisation criteria and colorectal cancer risk in people with Serrated Polyposis Syndrome: an Australian case-control study
11. Evaluating Multiple Next-Generation Sequencing–Derived Tumor Features to Accurately Predict DNA Mismatch Repair Status
12. Associations between pathological features and risk of metachronous colorectal cancer.
13. Intratumoral presence of the genotoxic gut bacteria pks+ E. coli, Enterotoxigenic Bacteroides fragilis, and Fusobacterium nucleatum and their association with clinicopathological and molecular features of colorectal cancer
14. Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study
15. Epithelial Neoplasms of the Large Bowel
16. Inherited BRCA1 and RNF43 pathogenic variants in a familial colorectal cancer type X family
17. DNA Mismatch Repair Gene Variant Classification: Evaluating the Utility of Somatic Mutations and Mismatch Repair Deficient Colonic Crypts and Endometrial Glands
18. Spectrum of gastrointestinal tract pathology in a multicenter cohort of 43 Cowden syndrome patients
19. An update on the morphology and molecular pathology of serrated colorectal polyps and associated carcinomas
20. Type 2 diabetes mellitus, blood cholesterol, triglyceride and colorectal cancer risk in Lynch syndrome
21. Ability of known susceptibility SNPs to predict colorectal cancer risk for persons with and without a family history
22. Identifying primary and secondary MLH1 epimutation carriers displaying low-level constitutional MLH1 methylation using droplet digital PCR and genome-wide DNA methylation profiling of colorectal cancers
23. Identification of a Proliferation Gene Cluster Associated with HPV E6/E7 Expression Level and Viral DNA Load in Invasive Cervical Carcinoma
24. The role of APC in WNT pathway activation in serrated neoplasia
25. DNA mismatch repair protein deficient non-neoplastic colonic crypts: a novel indicator of Lynch syndrome
26. Sessile serrated adenomas with dysplasia: morphological patterns and correlations with MLH1 immunohistochemistry
27. A mosaic pathogenic variant in MSH6 causes MSH6-deficient colorectal and endometrial cancer in a patient classified as suspected Lynch syndrome: a case report
28. Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1
29. Supplemental Table 1 from Association of the Colorectal CpG Island Methylator Phenotype with Molecular Features, Risk Factors, and Family History
30. Supplementary Tables from SNP rs16906252C>T Is an Expression and Methylation Quantitative Trait Locus Associated with an Increased Risk of Developing MGMT-Methylated Colorectal Cancer
31. Supplementary Figures from SNP rs16906252C>T Is an Expression and Methylation Quantitative Trait Locus Associated with an Increased Risk of Developing MGMT-Methylated Colorectal Cancer
32. Data from Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer
33. Appendix - clean version from Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer
34. Supplementary Tables from Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer
35. Supplementary Methods from SNP rs16906252C>T Is an Expression and Methylation Quantitative Trait Locus Associated with an Increased Risk of Developing MGMT-Methylated Colorectal Cancer
36. Genotoxic colibactin mutational signature in colorectal cancer is associated with clinicopathological features, specific genomic alterations and better survival
37. Evaluating Multiple Next-Generation Sequencing–Derived Tumor Features to Accurately Predict DNA Mismatch Repair Status
38. Additional file 1 of A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
39. A clinicopathological and molecular analysis of 200 traditional serrated adenomas
40. Quantitative Pathologic Analysis of Digitized Images of Colorectal Carcinoma Improves Prediction of Recurrence-Free Survival
41. Germline mutations inWNK2could be associated with serrated polyposis syndrome
42. Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomas
43. RNF43 is mutated less frequently in Lynch Syndrome compared with sporadic microsatellite unstable colorectal cancers
44. Histopathological findings of extra-ileal manifestations at initial diagnosis of Crohn’s disease-related ileitis
45. Should the grading of colorectal adenocarcinoma include microsatellite instability status?
46. Cystic lesions of the retrorectal space
47. Serrated colorectal polyps and polyposis
48. Associations of alcohol intake, smoking, physical activity and obesity with survival following colorectal cancer diagnosis by stage, anatomic site and tumor molecular subtype
49. The Role of the Surgical Pathologist in the Diagnosis of Gastrointestinal Polyposis Syndromes
50. Expression of MUC2, MUC5AC, MUC5B, and MUC6 mucins in colorectal cancers and their association with the CpG island methylator phenotype
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