For: |
Sheng JQ, Cui WJ, Fu L, Jin P, Han Y, Li SJ, Fan RY, Li AQ, Zhang MZ, Li SR. |
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URL: | https://www.wjgnet.com/1007-9327/full/v16/i12/1522.htm |
Number | Citing Articles |
1 |
Yong-Jun Tang, Kai Hu, Wei-Hua Huang, Chong-Zhi Wang, Zhi Liu, Yao Chen, Dong-Sheng Ouyang, Zhi-Rong Tan, Hong-Hao Zhou, Chun-Su Yuan. Effects of FMO3 Polymorphisms on Pharmacokinetics of Sulindac in Chinese Healthy Male Volunteers. BioMed Research International 2017; 2017: 1 doi: 10.1155/2017/4189678
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2 |
Chen-Guang Li, Lang Yang, Jian-Qiu Sheng. Hereditary Colorectal Cancer in China: Current Status and Progress. Gastrointestinal Tumors 2015; 2(3): 98 doi: 10.1159/000434650
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3 |
Chen‐Guang Li, Peng Jin, Lang Yang, Wan‐Chun Zang, Qian Kang, Na Li, Yuqi He, Junfeng Xu, Chen Zhang, Xin Wang, Jian‐Qiu Sheng. Germline mutations in patients with multiple colorectal polyps in China. Journal of Gastroenterology and Hepatology 2017; 32(10): 1723 doi: 10.1111/jgh.13776
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4 |
Minghui Pang, Yijun Liu, Xiaolin Hou, Jialiang Yang, Xuelai He, Nengyi Hou, Peixi Liu, Luo Liang, Junwen Fu, Kang Wang, Zimeng Ye, Bo Gong. A novel APC mutation identified in a large Chinese family with familial adenomatous polyposis and a brief literature review. Molecular Medicine Reports 2018; doi: 10.3892/mmr.2018.9130
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5 |
Lei Shi, Ruigao Song, Xiaolei Yao, Youshe Ren. Effects of selenium on the proliferation, apoptosis and testosterone production of sheep Leydig cells in vitro. Theriogenology 2017; 93: 24 doi: 10.1016/j.theriogenology.2017.01.022
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6 |
Hanifa J. Abu‐Toamih Atamni, Fuad A. Iraqi. Efficient protocols and methods for high‐throughput utilization of the Collaborative Cross mouse model for dissecting the genetic basis of complex traits. Animal Models and Experimental Medicine 2019; 2(3): 137 doi: 10.1002/ame2.12074
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7 |
Vittoria Disciglio, Giovanna Forte, Candida Fasano, Paola Sanese, Martina Lepore Signorile, Katia De Marco, Valentina Grossi, Filomena Cariola, Cristiano Simone. APC Splicing Mutations Leading to In-Frame Exon 12 or Exon 13 Skipping Are Rare Events in FAP Pathogenesis and Define the Clinical Outcome. Genes 2021; 12(3): 353 doi: 10.3390/genes12030353
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8 |
Na Li, Qian Kang, Lang Yang, Xiao‐Jun Zhao, Li‐Jun Xue, Xin Wang, Ai‐Qin Li, Chen‐Guang Li, Jian‐Qiu Sheng. Clinical characterization and mutation spectrum in patients with familial adenomatous polyposis in China. Journal of Gastroenterology and Hepatology 2019; 34(9): 1497 doi: 10.1111/jgh.14704
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9 |
Nikhat Khan, Anuja Lipsa, Gautham Arunachal, Mukta Ramadwar, Rajiv Sarin. Novel mutations and phenotypic associations identified through APC, MUTYH, NTHL1, POLD1, POLE gene analysis in Indian Familial Adenomatous Polyposis cohort. Scientific Reports 2017; 7(1) doi: 10.1038/s41598-017-02319-6
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10 |
A. N. Loginova, Yu. A. Shelygin, V. P. Shubin, A. M. Kuzminov, D. Yu. Pikunov, T. A. Saveleva, A. S. Tsukanov. Large Rearrangements in Genes Responsible for Familial Adenomatous Polyposis, <i>MUTYH</i>-Associated Polyposis and Peutz–Jeghers Syndrome in Russian Patients. Russian Journal of Gastroenterology, Hepatology, Coloproctology 2023; 33(1): 59 doi: 10.22416/1382-4376-2023-33-1-59-67
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11 |
Shujie Zhang, Haisong Qin, Weigang Lv, Shiyu Luo, Jin Wang, Chunyun Fu, Ruiyu Ma, Yiping Shen, Shaoke Chen, Lingqian Wu. Novel and reported APC germline mutations in Chinese patients with familial adenomatous polyposis. Gene 2016; 577(2): 187 doi: 10.1016/j.gene.2015.11.034
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12 |
JUN YANG, WEI QING LIU, WEN LIANG LI, CHENG CHEN, ZHU ZHU, MIN HONG, ZHI QIANG WANG, JIAN DONG. Investigating polymorphisms by bioinformatics is a potential cost-effective method to screen for germline mutations in Chinese familial adenomatous polyposis patients. Oncology Letters 2016; 12(1): 421 doi: 10.3892/ol.2016.4646
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13 |
Hanifa J. Abu Toamih Atamni, Fuad A. Iraqi. Molecular-Genetic and Statistical Techniques for Behavioral and Neural Research. 2018; : 191 doi: 10.1016/B978-0-12-804078-2.00009-X
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14 |
Jing‐Yuan Fang, Yong Quan Shi, Ying Xuan Chen, Jing Nan Li, Jian Qiu Sheng. Chinese consensus on the prevention of colorectal cancer (2016, Shanghai). Journal of Digestive Diseases 2017; 18(2): 63 doi: 10.1111/1751-2980.12450
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15 |
Chinese consensus on prevention of colorectal neoplasia (2021, Shanghai). Journal of Digestive Diseases 2022; 23(2): 58 doi: 10.1111/1751-2980.13079
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16 |
M.O. Mauro, Daniele Sartori, Rodrigo Juliano Oliveira, Priscila Lumi Ishii, Mário Sérgio Mantovani, Lúcia Regina Ribeiro. Activity of selenium on cell proliferation, cytotoxicity, and apoptosis and on the expression of CASP9, BCL-XL and APC in intestinal adenocarcinoma cells. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 2011; 715(1-2): 7 doi: 10.1016/j.mrfmmm.2011.06.015
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17 |
Sulma I. Mohammed, Sanya Springfield, Rina Das. Cancer Epigenetics. Methods in Molecular Biology 2012; 863: 395 doi: 10.1007/978-1-61779-612-8_25
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18 |
Jun Yang, Qing Wei Liu, Liang Wen Li, Qiang Zhi Wang, Min Hong, Jian Dong. Familial adenomatous polyposis in China. Oncology Letters 2016; 12(6): 4877 doi: 10.3892/ol.2016.5330
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19 |
Payam Shahnazi Gerdehsang, Najmeh Ranji, Mojtaba Gorji, Safoura Pakizehkar, Ali Asghar Kiani, Saeed Veysi. New Mutations inAPCGene Among Familial Adenomatous Polyposis (FAP) Patients in Iran. International Journal of Human Genetics 2017; 17(4): 145 doi: 10.1080/09723757.2017.1421441
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20 |
Seyed Kazem Mirinezhad, Seyed Yaqoob Moaddab, Kourosh Masnadi Shirazi, Morteza Jabbarpour Bonyadi, Amir Taher Eftekharsadat, Sosan Mir Najead Grami, Mohammad Hossein Somi. Clinical and Genetic Characterization of Familial Adenomatous Polyposis: An Iranian Population Study. Iranian Red Crescent Medical Journal 2018; (In Press) doi: 10.5812/ircmj.64254
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21 |
Farzaneh Pouya, Afsaneh Mojtabanezhad Shariatpanahi, Kamran Ghaffarzadegan, Seyed Abbas Tabatabaee Yazdi, Hamed Golmohammadzadeh, Ghodratollah Soltani, Kian Aminian Toosi, Mohammad Amin Kerachian. A novel large germ line deletion in adenomatous polyposis coli (APC) gene associated with familial adenomatous polyposis. Molecular Genetics & Genomic Medicine 2018; 6(6): 1031 doi: 10.1002/mgg3.479
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22 |
A. S. Tsukanov, A. A. Barinov, V. P. Shubin, A. N. Loginova, T. A. Savelieva, D. Yu. Pikunov, A. M. Kuzminov, V. N. Kashnikov, A. V. Polyakov, Yu. A. Shelygin. Finding the Cause of Hereditary Disease in a Family with Adenomatous Polyposis: Why It Is Important to Accumulate Whole Exome Sequencing Data in the Russian Population. Russian Journal of Genetics 2021; 57(6): 734 doi: 10.1134/S1022795421060120
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23 |
Guibo Song, Yufeng Yuan, Fang Zheng, Na Yang. Novel insertion mutation p.Asp610GlyfsX23 in APC gene causes familial adenomatous polyposis in Chinese families. Gene 2013; 516(2): 204 doi: 10.1016/j.gene.2012.12.077
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24 |
Junfeng Zhou, Chengbo Liang, Duxin Qing, Yongjun Wang, Yuyong Tan, Xiaoliu Shi. A novel large deletion in APC gene associated with Gardner syndrome in a Chinese family. Revista Española de Enfermedades Digestivas 2020; doi: 10.17235/reed.2020.6974/2020
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