383 results on '"Walsh, Michael D."'
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2. Evaluating Multiple Next-Generation Sequencing–Derived Tumor Features to Accurately Predict DNA Mismatch Repair Status
3. Preparation and Characterization of Polyclonal Antibodies against Human Chaperonin 10
4. Supplementary Data from Lynch Syndrome–Associated Breast Cancers: Clinicopathologic Characteristics of a Case Series from the Colon Cancer Family Registry
5. Data from Lynch Syndrome–Associated Breast Cancers: Clinicopathologic Characteristics of a Case Series from the Colon Cancer Family Registry
6. Additional file 1 of A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
7. Expression of MUC2, MUC5AC, MUC5B, and MUC6 mucins in colorectal cancers and their association with the CpG island methylator phenotype
8. Immunophenotypic analysis of ovarian endometrioid adenocarcinoma: Correlation with KRAS mutation and the presence of endometriosis
9. Lynch syndrome-associated breast cancers do not overexpress chromosome 11-encoded mucins
10. Colorectal carcinomas with KRAS mutation are associated with distinctive morphological and molecular features
11. Jobs and Research-Related Outcomes from the NIST-ARRA Construction Grants
12. Tumor testing to identify lynch syndrome in two Australian colorectal cancer cohorts
13. KRAS mutations in ovarian low-grade endometrioid adenocarcinoma: association with concurrent endometriosis
14. Immunohistochemical testing of conventional adenomas for loss of expression of mismatch repair proteins in Lynch syndrome mutation carriers: a case series from the Australasian site of the colon cancer family registry
15. Evaluating multiple next-generation sequencing derived tumor features to accurately predict DNA mismatch repair status
16. Quality Assessment and Correlation of Microsatellite Instability and Immunohistochemical Markers among Population- and Clinic-Based Colorectal Tumors: Results from the Colon Cancer Family Registry
17. High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry
18. Re: Microsatellite Instability and BRAF Mutation Testing in Colorectal Cancer Prognostication
19. Lynch syndrome and cervical cancer
20. Detection of large scale 3′ deletions in the PMS2 gene amongst Colon-CFR participants: have we been missing anything?
21. Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome)
22. Mutation deep within an intron of MSH2 causes Lynch syndrome
23. The “Fas counterattack” is not an active mode of tumor immune evasion in colorectal cancer with high-level microsatellite instability
24. Role of tumour molecular and pathology features to estimate colorectal cancer risk for first-degree relatives
25. Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study
26. Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysis
27. GATA3: A promising marker for metastatic breast carcinoma in serous effusion specimens
28. The MUC13 cell surface mucin is highly expressed by human colorectal carcinomas
29. Pathology Features in Bethesda Guidelines Predict Colorectal Cancer Microsatellite Instability: A Population-Based Study
30. Colorectal cancer in hyperplastic polyposis syndrome: In search of the polyp of origin
31. Linkage to chromosome 2q32.2-q35 in families with serrated neoplasia
32. Improving identification of lynch syndrome patients: A comparison of research data with clinical records
33. High Prevalence of Sessile Serrated Adenomas With BRAF Mutations: A Prospective Study of Patients Undergoing Colonoscopy
34. The PCNA-associated factor KIAA0101/p15 PAF binds the potential tumor suppressor product p33ING1b
35. Body size and risk for colorectal cancers showing BRAF mutations or microsatellite instability: a pooled analysis
36. Heterogeneity of MUC1 expression by human breast carcinoma cell lines in vivo and in vitro
37. Erratum to: Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study
38. Adenomas in lynch syndrome: diagnostically useful?
39. Risks of Lynch Syndrome Cancers for MSH6 Mutation Carriers
40. Classifying MLH1 and MSH2Variants Using Bioinformatic Prediction, Splicing Assays, Segregation, and Tumor Characteristics
41. Evidence for BRAF mutation and variable levels of microsatellite instability in a syndrome of familial colorectal cancer
42. Familial Mutations in PMS2 Can Cause Autosomal Dominant Hereditary Nonpolyposis Colorectal Cancer
43. DNA methylation patterns in adenomas from FAP, multiple adenoma and sporadic colorectal carcinoma patients
44. The PCNA-associated factor KIAA0101/p15PAF binds the potential tumor suppressor product p33ING1b
45. Use of Molecular Tumor Characteristics to Prioritize Mismatch Repair Gene Testing in Early-Onset Colorectal Cancer
46. Histologically Based Methods for Detection of Mucin
47. Serrated morphology and frequent CPG island hypermethylation defines a novel syndrome of familial colorectal cancer with origins in the serrated pathway of tumour development
48. Cadherin/catenin complex appears to be intact in hepatocellular carcinomas from Australia and South Africa
49. Reciprocal relationship between methylation status and loss of heterozygosity at the p14 ARF locus in Australian and South African hepatocellular carcinomas
50. Immunohistochemistry Versus Microsatellite Instability Testing in Phenotyping Colorectal Tumors
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