about
STK11/LKB1 Peutz-Jeghers gene inactivation in intraductal papillary-mucinous neoplasms of the pancreasClinical and biological characteristics of cervical neoplasias with FGFR3 mutation.Exploration of global gene expression patterns in pancreatic adenocarcinoma using cDNA microarraysAberrant methylation of the 5' CpG island of TSLC1 is common in pancreatic ductal adenocarcinoma and is first manifest in high-grade PanlNsMYC activation associated with the integration of HPV DNA at the MYC locus in genital tumorsColorectal carcinomas with KRAS mutation are associated with distinctive morphological and molecular featuresPrevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer.Mesothelin is overexpressed in the vast majority of ductal adenocarcinomas of the pancreas: identification of a new pancreatic cancer marker by serial analysis of gene expression (SAGE).Overexpression of S100A4 in pancreatic ductal adenocarcinomas is associated with poor differentiation and DNA hypomethylation.Discovery of new markers of cancer through serial analysis of gene expression: prostate stem cell antigen is overexpressed in pancreatic adenocarcinoma.Findings in young adults at colonoscopy from a hospital service database auditFamily history of colorectal cancer in BRAF p.V600E-mutated colorectal cancer cases.Risk factors for colorectal cancer in patients with multiple serrated polyps: a cross-sectional case series from genetics clinicsCharacterisation of familial colorectal cancer Type X, Lynch syndrome, and non-familial colorectal cancerRole of tumour molecular and pathology features to estimate colorectal cancer risk for first-degree relatives.Clinical problems of colorectal cancer and endometrial cancer cases with unknown cause of tumor mismatch repair deficiency (suspected Lynch syndrome)Association between molecular subtypes of colorectal cancer and patient survivalPIK3CA activating mutation in colorectal carcinoma: associations with molecular features and survival.Germline Mutations in the Polyposis-Associated Genes BMPR1A, SMAD4, PTEN, MUTYH and GREM1 Are Not Common in Individuals with Serrated Polyposis Syndrome.Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome).High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registryAssociation of the colorectal CpG island methylator phenotype with molecular features, risk factors, and family historyOutcome in Advanced Ovarian Cancer following an Appropriate and Comprehensive Effort at Upfront Cytoreduction: A Twenty-Year Experience in a Single Cancer Institute.Phenotype and polyp landscape in serrated polyposis syndrome: a series of 100 patients from genetics clinicsMutation deep within an intron of MSH2 causes Lynch syndrome.Aspirin, Ibuprofen, and the Risk of Colorectal Cancer in Lynch Syndrome.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.Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomas.Clinicopathologic Risk Factor Distributions for MLH1 Promoter Region Methylation in CIMP-Positive Tumors.Risks of primary extracolonic cancers following colorectal cancer in lynch syndromeAbsence of PMS2 mutations in colon-CFR participants whose colorectal cancers demonstrate unexplained loss of MLH1 expressionMultiplicity and molecular heterogeneity of colorectal carcinomas in individuals with serrated polyposis.Germline mutations in PMS2 and MLH1 in individuals with solitary loss of PMS2 expression in colorectal carcinomas from the Colon Cancer Family Registry Cohort.Risks of colorectal and other cancers after endometrial cancer for women with Lynch syndromeSensitivity to CPT-11 of xenografted human colorectal cancers as a function of microsatellite instability and p53 status.Detection of large scale 3' deletions in the PMS2 gene amongst Colon-CFR participants: have we been missing anything?Association between hypermethylation of DNA repetitive elements in white blood cell DNA and early-onset colorectal cancer.Risk of colorectal cancer for carriers of mutations in MUTYH, with and without a family history of cancer.Using tumour pathology to identify people at high genetic risk of breast and colorectal cancers.Critical appraisal of the diagnosis of the sessile serrated adenoma.
P50
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P50
description
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Christophe Rosty
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Christophe Rosty
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Christophe Rosty
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Christophe Rosty
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Christophe Rosty
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Christophe Rosty
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Christophe Rosty
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Christophe Rosty
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Christophe Rosty
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Christophe Rosty
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Christophe Rosty
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Christophe Rosty
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Christophe Rosty
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Christophe Rosty
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P106
P21
P31
P496
0000-0001-7671-2651