For: | Wang XL, Yuan Y, Zhang SZ, Cai SR, Huang YQ, Jiang Q, Zheng S. Clinical and genetic characteristics of Chinese hereditary nonpolyposis colorectal cancer families. World J Gastroenterol 2006; 12(25): 4074-4077 [PMID: 16810763 DOI: 10.3748/wjg.v12.i25.4074] |
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URL: | https://www.wjgnet.com/1007-9327/full/v12/i25/4074.htm |
Number | Citing Articles |
1 |
Min‐Hoe Chew, Poh‐Koon Koh, Melinda Tan, Kiat‐Hon Lim, Loi Carol, Choong‐Leong Tang. Mismatch Repair Deficiency Screening via Immunohistochemical Staining in Young Asians with Colorectal Cancers. World Journal of Surgery 2013; 37(10): 2468 doi: 10.1007/s00268-013-2134-2
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2 |
Yanqun Liu, Min Hoe Chew, Xue Wei Goh, Soo Yong Tan, Carol Tien Tau Loi, Yuen Ming Tan, Hai Yang Law, Poh Koon Koh, Choong Leong Tang, Hiromu Suzuki. Systematic Study on Genetic and Epimutational Profile of a Cohort of Amsterdam Criteria-Defined Lynch Syndrome in Singapore. PLoS ONE 2014; 9(4): e94170 doi: 10.1371/journal.pone.0094170
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3 |
Xiaomei Zhang, Senqing Chen, Jun Yu, Yuanying Zhang, Min Lv, Ming Zhu. Analysis of human MutS homolog 2 missense mutations in patients with colorectal cancer. Oncology Letters 2018; doi: 10.3892/ol.2018.8161
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4 |
Dandan Li, Fulan Hu, Fan Wang, Binbin Cui, Xinshu Dong, Wencui Zhang, Chunqing Lin, Xia Li, Da Wang, Yashuang Zhao, Amanda Ewart Toland. Prevalence of Pathological Germline Mutations of hMLH1 and hMSH2 Genes in Colorectal Cancer. PLoS ONE 2013; 8(3): e51240 doi: 10.1371/journal.pone.0051240
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5 |
Min Zhang, Tianhui Chen. Overview on population screening for carriers with germline mutations in mismatch repair (MMR) genes in China. Hereditary Cancer in Clinical Practice 2021; 19(1) doi: 10.1186/s13053-021-00182-1
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6 |
Hui-Ling Yap, Wei-Shieng Chieng, Jasmine Rui-Chen Lim, Robert Seng-Cheong Lim, Ross Soo, Jiayi Guo, Soo-Chin Lee. Recurring MLH1 deleterious mutations in unrelated Chinese Lynch syndrome families in Singapore. Familial Cancer 2009; 8(2): 85 doi: 10.1007/s10689-008-9209-5
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7 |
Yen‐Ling Chen, Yuh‐Jyh Jong, Jerome Ferrance, Jan‐Sing Hsien, Chi‐Jen Shih, Chia‐Hsien Feng, Ming‐Tsang Wu, Shou‐Mei Wu. Single nucleotide polymorphism detection in the hMSH2 gene using conformation‐sensitive CE. ELECTROPHORESIS 2008; 29(3): 634 doi: 10.1002/elps.200700488
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8 |
Min‐Hoe Chew, Poh‐Koon Koh, Kheng‐Hong Ng, Jit‐Fong Lim, Kok‐Sun Ho, Boon‐Swee Ooi, Choong‐Leong Tang, Kong‐Weng Eu. PHENOTYPIC CHARACTERISTICS OF HEREDITARY NON‐POLYPOSIS COLORECTAL CANCER BY THE AMSTERDAM CRITERIA: AN ASIAN PERSPECTIVE. ANZ Journal of Surgery 2008; 78(7): 556 doi: 10.1111/j.1445-2197.2008.04570.x
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9 |
WENQIAN WEI, LEI LIU, JIAN CHEN, KE JIN, FAN JIANG, FANGQI LIU, RONG FAN, ZHE CHENG, MENG SHEN, CHENYI XUE, SANJUN CAI, YE XU, PENG NAN. RACIAL DIFFERENCES IN MLH1 AND MSH2 MUTATION: AN ANALYSIS OF YELLOW RACE AND WHITE RACE BASED ON THE INSIGHT DATABASE. Journal of Bioinformatics and Computational Biology 2010; 8(supp01): 111 doi: 10.1142/S0219720010005154
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10 |
Goswin Y. Meyer-Rochow, Janine M. Smith, Anne-Louise Richardson, Deborah J. Marsh, Stan B. Sidhu, Bruce G. Robinson, Diana E. Benn. Denaturing High Performance Liquid Chromatography Detection of SDHB, SDHD, and VHL Germline Mutations in Pheochromocytoma. Journal of Surgical Research 2009; 157(1): 55 doi: 10.1016/j.jss.2008.07.043
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11 |
Zhaofei Liu, Cunjing Jin, Zilin Yu, Jing Zhang, Yan Liu, Huiyun Zhao, Bing Jia, Fan Wang. Radioimmunotherapy of Human Colon Cancer Xenografts with 131I-Labeled Anti-CEA Monoclonal Antibody. Bioconjugate Chemistry 2010; 21(2): 314 doi: 10.1021/bc9003603
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12 |
Min Hoe Chew, Wah Siew Tan, Yanqun Liu, Peh Yean Cheah, Carol TT Loi, Choong Leong Tang. Genomics of Hereditary Colorectal Cancer: Lessons Learnt from 25 Years of the Singapore Polyposis Registry. Annals of the Academy of Medicine, Singapore 2015; 44(8): 290 doi: 10.47102/annals-acadmedsg.V44N8p290
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13 |
Kyoung-Jin Park, Dong Kyung Chang, Hee Cheol Kim, Jong-Won Kim. Germline Variants in MLH1, MSH2, and MSH6 in Korean Patients with Lynch Syndrome. Laboratory Medicine Online 2018; 8(4): 156 doi: 10.3343/lmo.2018.8.4.156
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14 |
MING ZHU, HUI-MEI CHEN, YA-PING WANG. Missense mutations of MLH1 and MSH2 genes detected in patients with gastrointestinal cancer are associated with exonic splicing enhancers and silencers. Oncology Letters 2013; 5(5): 1710 doi: 10.3892/ol.2013.1243
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15 |
Jan Kosinski, Inga Hinrichsen, Janusz M. Bujnicki, Peter Friedhoff, Guido Plotz. Identification of Lynch syndrome mutations in the MLH1-PMS2 interface that disturb dimerization and mismatch repair. Human Mutation 2010; 31(8): 975 doi: 10.1002/humu.21301
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16 |
Hye In Woo, Young Min Woo, Sollip Kim, Seung-Tae Lee, Chang-Seok Ki, Jong-Won Kim. Challenges in assessing pathogenicity based on frequency of variants in mismatch repair genes: an extreme case of a MSH2 variant and a meta-analysis. Gene 2014; 546(2): 421 doi: 10.1016/j.gene.2014.06.027
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17 |
Juntao Lang, Xiaoli Lan, Yu Liu, Xueyan Jin, Tao Wu, Xun Sun, Qiong Wen, Rui An. Targeting cancer stem cells with an 131 I-labeled anti-AC133 monoclonal antibody in human colorectal cancer xenografts. Nuclear Medicine and Biology 2015; 42(5): 505 doi: 10.1016/j.nucmedbio.2015.01.003
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18 |
Shoko Takeuchi, Manami Doi, Naoki Ikari, Masakazu Yamamoto, Toru Furukawa. Mutations in BRCA1, BRCA2, and PALB2, and a panel of 50 cancer-associated genes in pancreatic ductal adenocarcinoma. Scientific Reports 2018; 8(1) doi: 10.1038/s41598-018-26526-x
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19 |
Poh-Koon Koh, Min-Hoe Chew, Yan-Sheng Tan, Kiat-Hon Lim, Carol Loi, Choong-Leong Tang, Kong-Weng Eu. Preliminary Results of Mismatch Repair Deficiency Screening via Immunohistochemical Staining in Young Asian Colorectal Cancers. Proceedings of Singapore Healthcare 2010; 19(1): 3 doi: 10.1177/201010581001900102
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20 |
SUSAN RICHMAN. Deficient mismatch repair: Read all about it (Review). International Journal of Oncology 2015; 47(4): 1189 doi: 10.3892/ijo.2015.3119
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