Bi-Allelic Somatic Tumor Mutations Explain the Majority of Colorectal and Endometrial Cancer Cases with Defective Mismatch Repair without an Identifiable Germline Mutation or MLH1 Epigenetic Silencing

Haraldsdottir S.; Hempel H.; Tomsic J.; Pearlman R.; de la Chapelle A.; Pritchard C. C.

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Bi-Allelic Somatic Tumor Mutations Explain the Majority of Colorectal and Endometrial Cancer Cases with Defective Mismatch Repair without an Identifiable Germline Mutation or MLH1 Epigenetic Silencing

机译：双等位基因的体细胞肿瘤突变解释了大肠和子宫内膜癌病例，其中有不匹配的缺损修复或没有可识别的种系突变或MLH1表观遗传沉默

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《The Journal of molecular diagnostics: JMD》 |2014年第6期|共1页
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Haraldsdottir S.; Hempel H.; Tomsic J.; Pearlman R.; de la Chapelle A.; Pritchard C. C.;
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正文语种 eng
中图分类临床医学;
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1. Bi-Allelic Somatic Tumor Mutations Explain the Majority of Colorectal and Endometrial Cancer Cases with Defective Mismatch Repair without an Identifiable Germline Mutation or MLH1 Epigenetic Silencing [J] . Haraldsdottir S., Hempel H., Tomsic J., The Journal of molecular diagnostics: JMD . 2014,第6期

机译：双等位基因的体细胞肿瘤突变解释了大肠和子宫内膜癌病例，其中有不匹配的缺损修复或没有可识别的种系突变或MLH1表观遗传沉默
2. Tumor Mismatch Repair Immunohistochemistry and DNA MLH1 Methylation Testing of Patients With Endometrial Cancer Diagnosed at Age Younger Than 60 Years Optimizes Triage for Population-Level Germline Mismatch Repair Gene Mutation Testing [J] . Daniel D. Buchanan, Yen Y. Tan, Michael D. Walsh, Journal of Clinical Oncology . 2014,第2期

机译：肿瘤不匹配修复免疫组化和DNA MLH1患者的子宫内膜癌患者诊断为年龄小于60岁，优化了人口水平种系错匹配修复基因突变检测的分类
3. Does risk of endometrial cancer for women without a germline mutation in a DNA mismatch repair gene depend on family history of endometrial cancer or colorectal cancer? [J] . BharatiR., JenkinsM.A., LindorN.M., Gynecologic Oncology: An International Journal . 2014,第2期

机译：对于没有DNA错配修复基因种系突变的女性，子宫内膜癌的风险是否取决于子宫内膜癌或结直肠癌的家族史？
4. GERMLINE AND SOMATIC MUTATIONS OF APC GENE AND THE GENOTYPE-PHENOTYPE ANALYSIS IN FAP AND SPORADIC COLORECTAL CANCERS [C] . Xiaorong Liu, Department of Genetics, Xiangnian Shan, 第四届国际后基因组生命科学技术学术论坛 . 2006

机译：FAP和散发性大肠癌中APC基因的种系和体细胞突变以及基因型-表型分析
5. Evaluation of the accuracy of quantitative models in predicting Lynch syndrome (hereditary nonpolyposis colorectal cancer with defective DNA mismatch repair) mutations in a population-based sample of early-onset colorectal cancer patients [D] . Carpiniello, Lauren 2007

机译：在以人群为基础的早发性大肠癌患者样本中预测定量模型预测Lynch综合征（遗传性非息肉病性大肠直肠癌，DNA失配修复缺陷）的准确性
6. Tumor Mismatch Repair Immunohistochemistry and DNA MLH1 Methylation Testing of Patients With Endometrial Cancer Diagnosed at Age Younger Than 60 Years Optimizes Triage for Population-Level Germline Mismatch Repair Gene Mutation Testing [O] . Daniel D. Buchanan, Yen Y. Tan, Michael D. Walsh, -1

机译：年龄小于60岁的子宫内膜癌患者的肿瘤错配修复免疫组织化学和DNA MLH1甲基化测试优化了人群水平种系错配修复基因突变测试的分类。
7. Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing [O] . Buchanan, D D, Tan, Y Y, Walsh, M D, 2014

机译：年龄小于60岁的子宫内膜癌患者的肿瘤错配修复免疫组织化学和DNA MLH1甲基化测试可优化人群水平种系错配修复基因突变测试的分类

Bi-Allelic Somatic Tumor Mutations Explain the Majority of Colorectal and Endometrial Cancer Cases with Defective Mismatch Repair without an Identifiable Germline Mutation or MLH1 Epigenetic Silencing

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