about
Identification of genes expressed by immune cells of the colon that are regulated by colorectal cancer-associated variantsA human colon cancer cell capable of initiating tumour growth in immunodeficient miceExacerbated tissue destruction in DSS-induced acute colitis of OPN-null mice is associated with downregulation of TNF-alpha expression and non-programmed cell deathCombined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancersPlk4 is required for cytokinesis and maintenance of chromosomal stability.Specific variants in the MLH1 gene region may drive DNA methylation, loss of protein expression, and MSI-H colorectal cancer.Pathology features in Bethesda guidelines predict colorectal cancer microsatellite instability: a population-based study.A novel and rapid method of determining the effect of unclassified MLH1 genetic variants on differential allelic expressionThe genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial diseaseCafé-au-lait macules and pediatric malignancy caused by biallelic mutations in the DNA mismatch repair (MMR) gene PMS2.The microenvironment-specific transformation of adult stem cells models malignant triton tumors.High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registryHereditary nonpolyposis colorectal cancer--molecular basis.Tumor microsatellite instability in early onset gastric cancerSclerosing pancreatitis presenting as a periampullary tumour.ARID1A loss correlates with mismatch repair deficiency and intact p53 expression in high-grade endometrial carcinomasLynch syndrome in a predominantly Afrocentric population: a clinicopathological and genetic study.Digital pathology: Attitudes and practices in the Canadian pathology communityPrognostic significance of mesenteric tumor nodules in patients with stage III colorectal cancer.Pathological features of colorectal carcinomas in MYH-associated polyposis.Mucinous tumor of the appendix with limited peritoneal spread: is there a role for expectant observation?Review of findings in prophylactic gynaecological specimens in Lynch syndrome with literature review and recommendations for grossing.The histomorphology of Lynch syndrome-associated ovarian carcinomas: toward a subtype-specific screening strategy.Phenotypic and genotypic characterisation of biallelic mismatch repair deficiency (BMMR-D) syndrome.Mule Regulates the Intestinal Stem Cell Niche via the Wnt Pathway and Targets EphB3 for Proteasomal and Lysosomal Degradation.High-grade papillary cystadenocarcinoma of the tongue.Discordance in fibrosis staging between liver biopsy and transient elastography using the FibroScan XL probe.Prevalence of loss of expression of DNA mismatch repair proteins in primary epithelial ovarian tumors.Patients with Lynch syndrome mismatch repair gene mutations are at higher risk for not only upper tract urothelial cancer but also bladder cancer.Use of mismatch repair immunohistochemistry and microsatellite instability testing: exploring Canadian practices.Variable clonal repopulation dynamics influence chemotherapy response in colorectal cancer.Unifying diagnosis for adenomatous polyps, café-au-lait macules, and a brain mass?A histology-based model for predicting microsatellite instability in colorectal cancers.High frequency of hereditary colorectal cancer in Newfoundland likely involves novel susceptibility genes.Performance characteristics of a brief Family History Questionnaire to screen for Lynch syndrome in women with newly diagnosed endometrial cancer.Performance characteristics of screening strategies for Lynch syndrome in unselected women with newly diagnosed endometrial cancer who have undergone universal germline mutation testing.Comparison of clinical schemas and morphologic features in predicting Lynch syndrome in mutation-positive patients with endometrial cancer encountered in the context of familial gastrointestinal cancer registries.Genetic and clinical determinants of constitutional mismatch repair deficiency syndrome: report from the constitutional mismatch repair deficiency consortium.Venous invasion in colorectal cancer: impact of an elastin stain on detection and interobserver agreement among gastrointestinal and nongastrointestinal pathologists.Genetic testing for Lynch syndrome in the province of Ontario.
P50
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Aaron Pollett
@ast
Aaron Pollett
@en
Aaron Pollett
@es
Aaron Pollett
@nl
type
label
Aaron Pollett
@ast
Aaron Pollett
@en
Aaron Pollett
@es
Aaron Pollett
@nl
prefLabel
Aaron Pollett
@ast
Aaron Pollett
@en
Aaron Pollett
@es
Aaron Pollett
@nl
P1053
J-2308-2016
P106
P21
P31
P3829
P496
0000-0001-5121-8788