Biallelic ANKS6 null variants cause notable extrarenal phenotypes in a nephronophthisis patient and lead to hepatobiliary abnormalities by YAP1 deficiency
Liu, Keqiang, Chen, Ru, Wang, Xiaoying, Gong, Yiming, Shi, Jia, Gu, Beilin, Zhou, Ying, Cai, Wei
Published in Clinical genetics (01.12.2023)
Published in Clinical genetics (01.12.2023)
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MicroRNA-4516-mediated regulation of MAPK10 relies on 3′ UTR cis-acting variants and contributes to the altered risk of Hirschsprung disease
Wang, Yang, Jiang, Qian, Chakravarti, Aravinda, Cai, Hao, Xu, Ze, Wu, Wenjie, Gu, Beilin, Li, Long, Cai, Wei
Published in Journal of medical genetics (01.09.2020)
Published in Journal of medical genetics (01.09.2020)
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Intestinal Reg4 deficiency confers susceptibility to high-fat diet-induced liver steatosis by increasing intestinal fat absorption in mice
Wang, Ying, Yan, Weihui, Lu, Ying, Du, Jun, Tian, Xinbei, Wu, Bo, Peng, Shicheng, Gu, Beilin, Cai, Wei, Xiao, Yongtao
Published in JHEP reports (01.06.2023)
Published in JHEP reports (01.06.2023)
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Loss-of-function variants within LMOD1 actin-binding site 2 cause pediatric intestinal pseudo-obstruction by impairing protein stability and actin nucleation
Liu, Keqiang, Lu, Lina, Chen, Shanshan, Gu, Beilin, Cai, Hui, Wang, Ying, Cai, Wei
Published in The FASEB journal (01.03.2022)
Published in The FASEB journal (01.03.2022)
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Common variants of NRG1 and ITGB4 confer risk of Hirschsprung disease in Han Chinese population
Wei, Zhiliang, Yu, Xianxian, Wu, Wenjie, Bai, Meirong, Lu, Yanjiao, Song, Huanlei, Gong, Yiming, Gu, Beilin, Chu, Xun, Cai, Wei
Published in Journal of pediatric surgery (01.12.2020)
Published in Journal of pediatric surgery (01.12.2020)
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Genetic variants in RET , ARHGEF3 and CTNNAL1 , and relevant interaction networks, contribute to the risk of Hirschsprung disease
Wang, Yang, Jiang, Qian, Cai, Hao, Xu, Ze, Wu, Wenjie, Gu, Beilin, Li, Long, Cai, Wei
Published in Aging (Albany, NY.) (06.03.2020)
Published in Aging (Albany, NY.) (06.03.2020)
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Journal Article
MicroRNA-4516-mediated regulation of MAPK10 relies on 3’UTR cis-acting variants and contributes to the altered risk of Hirschsprung disease
Wang, Yang, Jiang, Qian, Chakravarti, Aravinda, Cai, Hao, Xu, Ze, Wu, Wenjie, Gu, Beilin, Li, Long, Cai, Wei
Published in Journal of medical genetics (17.02.2020)
Published in Journal of medical genetics (17.02.2020)
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Common genetic variants in GAL , GAP 43 and NRSN 1 and interaction networks confer susceptibility to Hirschsprung disease
Wang, Yang, Yan, Weihui, Wang, Jun, Zhou, Ying, Chen, Jie, Gu, Beilin, Cai, Wei
Published in Journal of cellular and molecular medicine (01.07.2018)
Published in Journal of cellular and molecular medicine (01.07.2018)
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