| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1019283609 |
| P356 | DOI | 10.1054/BJOC.1999.1014 |
| P8608 | Fatcat ID | release_5otoq3ofmneihkgw6jew6w3zji |
| P932 | PMC publication ID | 2374417 |
| P698 | PubMed publication ID | 10732761 |
| P5875 | ResearchGate publication ID | 12582974 |
| P50 | author | Jean-Pierre Pignon | Q57419648 |
| P2093 | author name string | P Lasser | |
| P Rougier | |||
| J Bénard | |||
| J C Sabourin | |||
| B Bressac-de Paillerets | |||
| I Lefrère | |||
| D Couturier | |||
| S Grandjouan | |||
| M L Le Bihan | |||
| B Dieumegard | |||
| Bellefqih | |||
| P2860 | cites work | Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis | Q22122362 |
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| Lessons from hereditary colorectal cancer | Q28131788 | ||
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| Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer | Q28253384 | ||
| The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer | Q28256988 | ||
| Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer | Q28257360 | ||
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| DNA sequence analysis of exons 2 through 11 and immunohistochemical staining are required to detect all known p53 alterations in human malignancies | Q71814434 | ||
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| Mutational analysis of MLH1 and MSH2 in 25 prospectively-acquired RER+ endometrial cancers | Q73157872 | ||
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| MLH1 and MSH2 constitutional mutations in colorectal cancer families not meeting the standard criteria for hereditary nonpolyposis colorectal cancer | Q74323855 | ||
| Regulation of intracellular beta-catenin levels by the adenomatous polyposis coli (APC) tumor-suppressor protein | Q29614383 | ||
| Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma | Q29615026 | ||
| Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumors and mismatch repair-defective human tumor cell lines | Q29620526 | ||
| p53 protein stability in tumour cells is not determined by mutation but is dependent on Mdm2 binding. | Q30428424 | ||
| A simple model for carcinogenesis of colorectal cancers with microsatellite instability. | Q33767129 | ||
| A naturally occurring hPMS2 mutation can confer a dominant negative mutator phenotype | Q33772742 | ||
| Excess beta-catenin promotes accumulation of transcriptionally active p53. | Q33891005 | ||
| Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis. | Q34732921 | ||
| Accumulated clonal genetic alterations in familial and sporadic colorectal carcinomas with widespread instability in microsatellite sequences | Q35753544 | ||
| Genetic instability in human ovarian cancer cell lines. | Q35791709 | ||
| Bcl-2 expression in normal endometrium during the menstrual cycle. | Q35834144 | ||
| RNA-based mutation screening in hereditary nonpolyposis colorectal cancer | Q35882089 | ||
| Alternative genetic pathways in colorectal carcinogenesis. | Q36637607 | ||
| Genetic instability occurs in the majority of young patients with colorectal cancer | Q38297232 | ||
| Alternative splicing of hMSH2 in normal human tissues | Q38346418 | ||
| Overview of natural history, pathology, molecular genetics and management of HNPCC (Lynch Syndrome). | Q40969554 | ||
| Familial risk and colon cancer | Q40969561 | ||
| Characterization of MLH1 and MSH2 alternative splicing and its relevance to molecular testing of colorectal cancer susceptibility | Q41061594 | ||
| Conditional mutator phenotypes in hMSH2-deficient tumor cell lines | Q41091724 | ||
| Hereditary nonpolyposis colorectal cancer (Lynch syndrome). An updated review | Q41127594 | ||
| Loss of DNA mismatch repair in acquired resistance to cisplatin | Q41189901 | ||
| Germline HNPCC gene variants have little influence on the risk for sporadic colorectal cancer | Q42005199 | ||
| MLH1, PMS1, and MSH2 interactions during the initiation of DNA mismatch repair in yeast | Q42427955 | ||
| Microsatellite instability and mutations of the transforming growth factor beta type II receptor gene in colorectal cancer | Q45345220 | ||
| Functional analysis of human MLH1 mutations in Saccharomyces cerevisiae | Q47713981 | ||
| Germ-line mutation of the hMSH6/GTBP gene in an atypical hereditary nonpolyposis colorectal cancer kindred | Q48044118 | ||
| BRCA1 mutations in primary breast and ovarian carcinomas | Q48078473 | ||
| Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer | Q48084125 | ||
| Tumour spectrum in hereditary non-polyposis colorectal cancer (HNPCC) and in families with "suspected HNPCC". A population-based study in northern Italy. Colorectal Cancer Study Group. | Q53389780 | ||
| Diagnostic microsatellite instability: definition and correlation with mismatch repair protein expression. | Q53439660 | ||
| Molecular nature of colon tumors in hereditary nonpolyposis colon cancer, familial polyposis, and sporadic colon cancer. | Q53452567 | ||
| Microsatellite instability analysis: a multicenter study for reliability and quality control. | Q54225696 | ||
| Somatic mutations in the BRCA1 gene in sporadic ovarian tumours. | Q54417578 | ||
| HNPCC associated with germline mutation in the TGF-beta type II receptor gene. | Q55067518 | ||
| Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group [published erratum appears in Hum Mol Genet 1998 May;7(5):941] | Q56893811 | ||
| Incidence of Hereditary Nonpolyposis Colorectal Cancer and the Feasibility of Molecular Screening for the Disease | Q57567959 | ||
| Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancer | Q57568035 | ||
| Analysis of mismatch repair genes in hereditary non–polyposis colorectal cancer patients | Q57570041 | ||
| A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: Meeting Highlights and Bethesda Guidelines | Q57978042 | ||
| K-ras andp53 mutations in hereditary non-polyposis colorectal cancers | Q61196108 | ||
| The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC) | Q62978412 | ||
| The tumour spectrum in hereditary non-polyposis colorectal cancer: A study of 24 kindreds in the netherlands | Q62978416 | ||
| Tumor variation in three extended Lynch syndrome II kindreds | Q68404297 | ||
| Extracolonic cancer in hereditary nonpolyposis colorectal cancer | Q70557907 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | colorectal cancer | Q188874 |
| colorectal carcinoma | Q25493920 | ||
| P304 | page(s) | 871-880 | |
| P577 | publication date | 2000-02-01 | |
| P1433 | published in | British Journal of Cancer | Q326309 |
| P1476 | title | Extensive molecular screening for hereditary non-polyposis colorectal cancer | |
| P478 | volume | 82 |
| Q36507457 | Accuracy of MSI testing in predicting germline mutations of MSH2 and MLH1: a case study in Bayesian meta-analysis of diagnostic tests without a gold standard |
| Q35700015 | An American founder mutation in MLH1. |
| Q59411242 | Assessing colorectal cancer mismatch repair status in the modern era: a survey of current practices and re-evaluation of the role of microsatellite instability testing |
| Q33513323 | Assessing pathogenicity of MLH1 variants by co-expression of human MLH1 and PMS2 genes in yeast |
| Q57569926 | Classification of ambiguous mutations in DNA mismatch repair genes identified in a population-based study of colorectal cancer |
| Q52005531 | Clinical and molecular biologic characteristics of early-onset versus late-onset colorectal carcinoma in Filipinos. |
| Q36178327 | Clinical characteristics and diagnosis of patients with hereditary nonpolyposis colorectal cancer |
| Q36415689 | Clinicopathological and molecular genetic analysis of 4 typical Chinese HNPCC families. |
| Q36643467 | Contrasting molecular pathology of colorectal carcinoma in Egyptian and Western patients |
| Q35748966 | Conventional and tissue microarray immunohistochemical expression analysis of mismatch repair in hereditary colorectal tumors |
| Q34568596 | DNA mismatch repair defects: role in colorectal carcinogenesis |
| Q61758596 | Efficacy and safety of a cisplatin and paclitaxel induction regimen followed by chemoradiotherapy for patients with locally advanced head and neck squamous cell carcinoma |
| Q93012448 | Functional interrogation of Lynch syndrome-associated MSH2 missense variants via CRISPR-Cas9 gene editing in human embryonic stem cells |
| Q34557954 | HMLH1 gene mutation in gastric cancer patients and their kindred |
| Q36451916 | Human mismatch repair protein hMutLα is required to repair short slipped-DNAs of trinucleotide repeats |
| Q36412420 | Human mutL homolog 1 expression characteristic and prognostic effect on patients with sporadic colorectal cancer |
| Q35760971 | Identification of mismatch repair gene mutations in young patients with colorectal cancer and in patients with multiple tumours associated with hereditary non-polyposis colorectal cancer. |
| Q80186521 | Immunohistochemical staining of hMLH1 and hMSH2 reflects microsatellite instability status in ovarian carcinoma |
| Q36492931 | Immunohistochemistry and microsatellite instability analysis in molecular subtyping of colorectal carcinoma based on mismatch repair competency |
| Q39514722 | Immunohistochemistry versus microsatellite instability testing for screening colorectal cancer patients at risk for hereditary nonpolyposis colorectal cancer syndrome. Part I. The utility of immunohistochemistry |
| Q38661498 | Investigation of correlation between mutational status in key EGFR signaling genes and prognosis of stage II colorectal cancer |
| Q34579284 | Is reduced expression of mismatch repair genes MLH1 and MSH2 in patients with sporadic colorectal cancer related to their prognosis? |
| Q35057393 | Mismatch repair protein expression in colorectal cancer |
| Q42379696 | Molecular analysis: microsatellity instability and loss of heterozygosity of tumor suppressor gene in hereditary non-polyposis colorectal cancers (HNPCC). |
| Q36821500 | Oligonucleotide-directed mutagenesis screen to identify pathogenic Lynch syndrome-associated MSH2 DNA mismatch repair gene variants |
| Q30906288 | Partial loss of heterozygosity events at the mutated gene in tumors from MLH1/MSH2 large genomic rearrangement carriers |
| Q48375665 | Performance of Lynch syndrome predictive models in quantifying the likelihood of germline mutations in patients with abnormal MLH1 immunoexpression |
| Q36882484 | Prediction of germline mutations and cancer risk in the Lynch syndrome |
| Q34633911 | Prevalence of pathological germline mutations of hMLH1 and hMSH2 genes in colorectal cancer |
| Q30413890 | Q48P mutation in the hMLH1 gene associated with Lynch syndrome in three Hungarian families |
| Q35904483 | The utility of immunohistochemical detection of DNA mismatch repair gene proteins. |
| Q36246500 | Use of microsatellite instability and immunohistochemistry testing for the identification of individuals at risk for Lynch syndrome |
| Q81160714 | Value of microsatellite instability typing in detecting hereditary non-polyposis colorectal cancer. A prospective multicentric study by the Association Aquitaine Gastro |
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