For: | Sheng JQ, Zhang H, Ji M, Fu L, Mu H, Zhang MZ, Huang JS, Han M, Li AQ, Wei Z, Sun ZQ, Wu ZT, Xia CH, Li SR. Genetic diagnosis strategy of hereditary non-polyposis colorectal cancer. World J Gastroenterol 2009; 15(8): 983-989 [PMID: 19248199 DOI: 10.3748/wjg.15.983] |
---|---|
URL: | https://www.wjgnet.com/1007-9327/full/v15/i8/983.htm |
Number | Citing Articles |
1 |
XIA LI, YIBAINA WANG, ZUOMING ZHANG, XIAOPING YAO, JIE GE, YASHUANG ZHAO. Correlation of MLH1 and MGMT methylation levels between peripheral blood leukocytes and colorectal tissue DNA samples in colorectal cancer patients. Oncology Letters 2013; 6(5): 1370 doi: 10.3892/ol.2013.1543
|
2 |
Muhammad Usman Rashid, Humaira Naeemi, Noor Muhammad, Asif Loya, Jan Lubiński, Anna Jakubowska, Muhammed Aasim Yusuf. Prevalence and spectrum of MLH1, MSH2, and MSH6 pathogenic germline variants in Pakistani colorectal cancer patients. Hereditary Cancer in Clinical Practice 2019; 17(1) doi: 10.1186/s13053-019-0128-2
|
3 |
Angela N. Bartley, Rajyalakshmi Luthra, Devki S. Saraiya, Diana L. Urbauer, Russell R. Broaddus. Identification of Cancer Patients with Lynch Syndrome: Clinically Significant Discordances and Problems in Tissue-Based Mismatch Repair Testing. Cancer Prevention Research 2012; 5(2): 320 doi: 10.1158/1940-6207.CAPR-11-0288
|
4 |
Sang-Bong Jung, Han-IL Lee, Hoon-Kyu Oh, Im-Hee Shin, Chang-Ho Jeon. Clinico-pathologic Parameters for Prediction of Microsatellite Instability in Colorectal Cancer. Cancer Research and Treatment 2012; 44(3): 179 doi: 10.4143/crt.2012.44.3.179
|
5 |
Huidan Zhang, Lianfeng Shan, Xiaonan Wang, Qian Ma, Jin Fang. A novel bisulfite-microfluidic temperature gradient capillary electrophoresis platform for highly sensitive detection of gene promotermethylation. Biosensors and Bioelectronics 2013; 42: 503 doi: 10.1016/j.bios.2012.10.013
|
6 |
Lei Fu, Jian-qiu Sheng, Xiao-ou Li, Peng Jin, Hong Mu, Min Han, Ji-sheng Huang, Zi-qin Sun, Ai-qin Li, Zi-tao Wu, Shi-rong Li. Mismatch repair gene mutation analysis and colonoscopy surveillance in Chinese lynch syndrome families. Cellular Oncology 2013; 36(3): 225 doi: 10.1007/s13402-013-0130-z
|
7 |
Kandelaria Rumilla, Karen V. Schowalter, Noralane M. Lindor, Brittany C. Thomas, Kara A. Mensink, Steven Gallinger, Spring Holter, Polly A. Newcomb, John D. Potter, Mark A. Jenkins, John L. Hopper, Tiffany I. Long, Daniel J. Weisenberger, Robert W. Haile, Graham Casey, Peter W. Laird, Loic Le Marchand, Stephen N. Thibodeau. Frequency of Deletions of EPCAM (TACSTD1) in MSH2-Associated Lynch Syndrome Cases. The Journal of Molecular Diagnostics 2011; 13(1): 93 doi: 10.1016/j.jmoldx.2010.11.011
|
8 |
Jun-Yu Lu, Jian-Qiu Sheng. Advances in the study of Lynch syndrome in China. World Journal of Gastroenterology 2015; 21(22): 6861-6871 doi: 10.3748/wjg.v21.i22.6861
|