458 results on '"Clendenning, Mark"'
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. Rare germline variants in the AXIN2 gene in families with colonic polyposis and colorectal cancer
6. Informed choice and attitudes regarding a genomic test to predict risk of colorectal cancer in general practice
7. Identifying colorectal cancer caused by biallelic MUTYH pathogenic variants using tumor mutational signatures
8. 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
9. Evaluating Multiple Next-Generation Sequencing–Derived Tumor Features to Accurately Predict DNA Mismatch Repair Status
10. 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
11. A Genomic Test for Colorectal Cancer Risk : Is This Acceptable and Feasible in Primary Care?
12. Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study
13. Inherited BRCA1 and RNF43 pathogenic variants in a familial colorectal cancer type X family
14. DNA Mismatch Repair Gene Variant Classification: Evaluating the Utility of Somatic Mutations and Mismatch Repair Deficient Colonic Crypts and Endometrial Glands
15. Mismatch repair gene pathogenic germline variants in a population-based cohort of breast cancer
16. Type 2 diabetes mellitus, blood cholesterol, triglyceride and colorectal cancer risk in Lynch syndrome
17. Ability of known susceptibility SNPs to predict colorectal cancer risk for persons with and without a family history
18. 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
19. 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.
20. A mosaic pathogenic variant in MSH6 causes MSH6-deficient colorectal and endometrial cancer in a patient classified as suspected Lynch syndrome: a case report
21. Physical mapping and characterisation of the chicken natural killer complex
22. Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1
23. Supplemental Table 1 from Association of the Colorectal CpG Island Methylator Phenotype with Molecular Features, Risk Factors, and Family History
24. Supplementary Data from Lynch Syndrome–Associated Breast Cancers: Clinicopathologic Characteristics of a Case Series from the Colon Cancer Family Registry
25. 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
26. 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
27. Data from Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer
28. Data from Lynch Syndrome–Associated Breast Cancers: Clinicopathologic Characteristics of a Case Series from the Colon Cancer Family Registry
29. Supplementary Tables from Identification of Novel Variants in Colorectal Cancer Families by High-Throughput Exome Sequencing
30. Appendix - clean version from Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer
31. Supplementary Figure 1 from Identification of Novel Variants in Colorectal Cancer Families by High-Throughput Exome Sequencing
32. Supplementary Tables from Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer
33. Supplementary Figure 2 from Identification of Novel Variants in Colorectal Cancer Families by High-Throughput Exome Sequencing
34. Description of supplementary files from Identification of Novel Variants in Colorectal Cancer Families by High-Throughput Exome Sequencing
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. Supplementary Table 1 from Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients
37. Supplementary Table 2 from Origins and Prevalence of the American Founder Mutation of MSH2
38. Supplementary Figure 1 from Origins and Prevalence of the American Founder Mutation of MSH2
39. Supplementary Table 1 from Origins and Prevalence of the American Founder Mutation of MSH2
40. Data from Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients
41. Supplementary Table 2 from Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients
42. Genotoxic colibactin mutational signature in colorectal cancer is associated with clinicopathological features, specific genomic alterations and better survival
43. Evaluating Multiple Next-Generation Sequencing–Derived Tumor Features to Accurately Predict DNA Mismatch Repair Status
44. Additional file 1 of A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
45. Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomas
46. RNF43 is mutated less frequently in Lynch Syndrome compared with sporadic microsatellite unstable colorectal cancers
47. Should the grading of colorectal adenocarcinoma include microsatellite instability status?
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. Expression of MUC2, MUC5AC, MUC5B, and MUC6 mucins in colorectal cancers and their association with the CpG island methylator phenotype
50. Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.