about
Molecular models for the tissue specificity of DNA mismatch repair-deficient carcinogenesisA review of the clinical relevance of mismatch-repair deficiency in ovarian cancerSurvey of HNPCC Management Analysis of Responses from 18 International Cancer Centres.The Association of the COMT V158M Polymorphism with Endometrial/Ovarian Cancer in HNPCC Families Adhering to the Amsterdam Criteria.Frequency of the Common MYH Mutations (G382D and Y165C) in MMR Mutation Positive and Negative HNPCC Patients.Mismatch repair protein expression and colorectal cancer in Hispanics from Puerto RicoApplication of molecular diagnostics for the detection of Lynch syndrome.Clinical and molecular analysis of hereditary non-polyposis colorectal cancer in Chinese colorectal cancer patients.Features of ovarian cancer in Lynch syndrome (Review).A role for DNA mismatch repair protein Msh2 in error-prone double-strand-break repair in mammalian chromosomesGenetics and pathology of pancreatic cancer.Ovarian cancer risk is associated with a common variant in the promoter sequence of the mismatch repair gene MLH1The inherited genetics of ovarian and endometrial cancer.Hereditary ovarian carcinoma: heterogeneity, molecular genetics, pathology, and management.Phenotypic heterogeneity in hereditary non-polyposis colorectal cancer: identical germline mutations associated with variable tumour morphology and immunohistochemical expression.Accurate homologous recombination is a prominent double-strand break repair pathway in mammalian chromosomes and is modulated by mismatch repair protein Msh2.Frequency of mutations in mismatch repair genes in a population-based study of women with ovarian cancer.High risk of colorectal and endometrial cancer in Ashkenazi families with the MSH2 A636P founder mutation.Systematic review and meta-analysis of ovarian cancers: estimation of microsatellite-high frequency and characterization of mismatch repair deficient tumor histology.Sampling strategies for tissue microarrays to evaluate biomarkers in ovarian cancer.Detection of hMSH2 and hMLH1 mutations in Chinese hereditary non-polyposis colorectal cancer kindreds.Calculation of risk of colorectal and endometrial cancer among patients with Lynch syndrome.History, genetics, and strategies for cancer prevention in Lynch syndrome.Review of findings in prophylactic gynaecological specimens in Lynch syndrome with literature review and recommendations for grossing.Müllerian intra-abdominal carcinomatosis in hereditary breast ovarian cancer syndrome: implications for risk-reducing surgery.A mobile colonoscopic unit for lynch syndrome: trends in surveillance uptake and patient experiences of screening in a developing country.Reproductive Decision-Making in MMR Mutation Carriers After Results Disclosure: Impact of Psychological Status in Childbearing Options.Expression of cancer related BRCA1 missense variants decreases MMS-induced recombination in Saccharomyces cerevisiae without altering its nuclear localization.
P2860
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P2860
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
2001年论文
@zh
2001年论文
@zh-cn
name
Cancer risk in mismatch repair gene mutation carriers.
@ast
Cancer risk in mismatch repair gene mutation carriers.
@en
type
label
Cancer risk in mismatch repair gene mutation carriers.
@ast
Cancer risk in mismatch repair gene mutation carriers.
@en
prefLabel
Cancer risk in mismatch repair gene mutation carriers.
@ast
Cancer risk in mismatch repair gene mutation carriers.
@en
P356
P1433
P1476
Cancer risk in mismatch repair gene mutation carriers.
@en
P2093
P2888
P356
10.1023/A:1011590617833
P577
2001-01-01T00:00:00Z
P5875
P6179
1034332690