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Cited by in CrossRef
For: Liu HX, Li Y, Jiang XD, Yin HN, Zhang L, Wang Y, Yang J. Mutation screening of mismatch repair gene Mlh3 in familial esophageal cancer. World J Gastroenterol 2006; 12(33): 5281-5286 [PMID: 16981255 DOI: 10.3748/wjg.v12.i33.5281]
URL: https://www.wjgnet.com/1007-9327/full/v12/i33/5281.htm
Number Citing Articles
1
Feng Ye, Qi Cheng, Jiajie Shen, Caiyun Zhou, Huaizeng Chen, William B. Coleman. Mismatch Repair Gene MLH3 Pro844Leu and Thr942Ile Polymorphisms and the Susceptibility to Cervical Carcinoma and HPV Infection: A Case-Control Study in a Chinese PopulationPLoS ONE 2014; 9(4): e96224 doi: 10.1371/journal.pone.0096224
2
Carson J. Miller, Geum-Yi Kim, Xiaonan Zhao, Karen Usdin, Sue Jinks-Robertson. All three mammalian MutL complexes are required for repeat expansion in a mouse cell model of the Fragile X-related disordersPLOS Genetics 2020; 16(6): e1008902 doi: 10.1371/journal.pgen.1008902
3
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 PheochromocytomaJournal of Surgical Research 2009; 157(1): 55 doi: 10.1016/j.jss.2008.07.043
4
Xiao-Yun Yang, Hai Yu, Ming-Rong Xi, Kai-Xuan Yang, Xiao-Ling Pan, Ming Hu, Zhi-Lan Peng. Association of the ARLTS1 Variants With Familial Ovarian Cancer Risk in ChinaInternational Journal of Gynecological Cancer 2009; 19(4): 585 doi: 10.1111/IGC.0b013e3181a39d03
5
Mari K. Korhonen, Elina Vuorenmaa, Minna Nyström. The first functional study of MLH3 mutations found in cancer patientsGenes, Chromosomes and Cancer 2008; 47(9): 803 doi: 10.1002/gcc.20581
6
Jianghua Ou, Merete Rasmussen, Helga Westers, Sofie D. Andersen, Paul O. Jager, Krista A. Kooi, Renée C. Niessen, Bart J. L. Eggen, Finn C. Nielsen, Jan H. Kleibeuker, Rolf H. Sijmons, Lene J. Rasmussen, Robert M. W. Hofstra. Biochemical characterization of MLH3 missense mutations does not reveal an apparent role of MLH3 in Lynch syndromeGenes, Chromosomes and Cancer 2009; 48(4): 340 doi: 10.1002/gcc.20644