scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1047702561 |
P356 | DOI | 10.1186/1756-8722-6-22 |
P932 | PMC publication ID | 3623651 |
P698 | PubMed publication ID | 23531335 |
P5875 | ResearchGate publication ID | 236082953 |
P2093 | author name string | Jie Li | |
Yue Wang | |||
Setsuko K Chambers | |||
Wenxin Zheng | |||
Kenneth Hatch | |||
Yiying Wang | |||
Janiel Cragun | |||
P2860 | cites work | The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations | Q24655454 |
Current and emerging trends in Lynch syndrome identification in women with endometrial cancer. | Q33738168 | ||
Prevalence of defective DNA mismatch repair and MSH6 mutation in an unselected series of endometrial cancers | Q35022384 | ||
Role of DNA mismatch repair defects in the pathogenesis of human cancer | Q35085461 | ||
Mutations associated with HNPCC predisposition -- Update of ICG-HNPCC/INSiGHT mutation database | Q35940640 | ||
Gynecologic Cancers in Lynch Syndrome/HNPCC. | Q36246496 | ||
Prediction of germline mutations and cancer risk in the Lynch syndrome | Q36882484 | ||
The risk of extra-colonic, extra-endometrial cancer in the Lynch syndrome. | Q37064547 | ||
Carcinoma of the lower uterine segment: a newly described association with Lynch syndrome | Q37103142 | ||
Endometrial cancer as a familial tumor: pathology and molecular carcinogenesis (review). | Q37236178 | ||
Endometrial carcinomas in women aged 40 years and younger: tumors associated with loss of DNA mismatch repair proteins comprise a distinct clinicopathologic subset | Q37629522 | ||
Microsatellite instability and colorectal cancer | Q37942234 | ||
Identification of individuals at risk for Lynch syndrome using targeted evaluations and genetic testing: National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Colorectal Cancer joint practice guideline | Q37968220 | ||
Explaining the familial colorectal cancer risk associated with mismatch repair (MMR)-deficient and MMR-stable tumors | Q38464726 | ||
Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance | Q47243772 | ||
Lynch syndrome--related endometrial carcinomas show a high frequency of nonendometrioid types and of high FIGO grade endometrioid types | Q47795729 | ||
Clinical features of colorectal carcinoma in cancer family syndrome. | Q50577948 | ||
Gynecologic cancer as a "sentinel cancer" for women with hereditary nonpolyposis colorectal cancer syndrome. | Q50776571 | ||
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. | Q51552333 | ||
Selection of endometrial carcinomas for DNA mismatch repair protein immunohistochemistry using patient age and tumor morphology enhances detection of mismatch repair abnormalities. | Q51803437 | ||
Role of heredity in multiple primary cancer | Q52807270 | ||
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Uterine carcinosarcoma associated with hereditary nonpolyposis colorectal cancer. | Q53565868 | ||
Life-time risk of different cancers in hereditary non-polyposis colorectal cancer (HNPCC) syndrome. | Q54598204 | ||
Lynch syndrome: form, function, proteins, and basketball | Q56649581 | ||
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Prediction of MLH1 and MSH2 Mutations in Lynch Syndrome | Q57260018 | ||
Prospective Determination of Prevalence of Lynch Syndrome in Young Women With Endometrial Cancer | Q60167347 | ||
Pathologic features of endometrial carcinoma associated with HNPCC | Q60167348 | ||
Women With Synchronous Primary Cancers of the Endometrium and Ovary: Do They Have Lynch Syndrome? | Q60167351 | ||
Carcinoma of the endometrium. II. Papillary adenocarcinoma: a clinical pathological study, 46 cases | Q70362144 | ||
Diagnostic use of microsatellite instability in hereditary non-polyposis colorectal cancer | Q71520203 | ||
Hereditary colorectal cancer | Q73088287 | ||
Microsatellite instability in endometrioid endometrial carcinoma: correlation with clinically relevant pathologic variables | Q79799792 | ||
Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients | Q80050907 | ||
Comment on: Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients | Q81381640 | ||
P921 | main subject | Lynch syndrome | Q783644 |
endometrial cancer | Q944777 | ||
P304 | page(s) | 22 | |
P577 | publication date | 2013-03-25 | |
P1433 | published in | Journal of Hematology & Oncology | Q15724593 |
P1476 | title | Lynch syndrome related endometrial cancer: clinical significance beyond the endometrium | |
P478 | volume | 6 |
Q91895870 | Comparison of screening strategies for Lynch syndrome in patients with newly diagnosed endometrial cancer: a prospective cohort study in China |
Q36059087 | Do hereditary syndrome-related gynecologic cancers have any specific features? |
Q92137491 | Exome-Wide Rare Variant Analysis From the DiscovEHR Study Identifies Novel Candidate Predisposition Genes for Endometrial Cancer |
Q37512381 | Genetic screening in young women diagnosed with endometrial cancer. |
Q37597246 | Hereditary cancer syndromes in Latino populations: genetic characterization and surveillance guidelines |
Q92151317 | PMS2 germline mutation c.1577delA (p.Asp526Alafs*69)-induced Lynch syndrome-associated endometrial cancer: A case report |
Q90399148 | Pathogenesis and Clinical Management of Uterine Serous Carcinoma |
Q64997225 | Prognostic implications of mismatch repair deficiency in patients with nonmetastatic colorectal and endometrial cancer. |
Q37382351 | Understanding Molecular Landscape of Endometrial Cancer through Next Generation Sequencing: What We Have Learned so Far? |
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