Genetic variants in RET, ARHGEF3 and CTNNAL1, and relevant interaction networks, contribute to the risk of Hirschsprung disease-Reference-Cited by-同舟云学术

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Genetic variants in RET, ARHGEF3 and CTNNAL1, and relevant interaction networks, contribute to the risk of Hirschsprung disease

Published:2020-03-06 Issue:5 Volume:12 Page:4379-4393
ISSN:1945-4589
Container-title:Aging
language:en
Short-container-title:Aging

Author:

Wang Yang¹²³,Jiang Qian⁴,Cai Hao¹²³,Xu Ze¹²³,Wu Wenjie¹²³,Gu Beilin¹²³,Li Long⁵,Cai Wei¹²³

Affiliation:

1. Department of Pediatric Surgery, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China

2. Shanghai Key Laboratory of Pediatric Gastroenterology and Nutrition, Shanghai, China

3. Shanghai Institute for Pediatric Research, Shanghai, China

4. Department of Medical Genetics, Capital Institute of Pediatrics, Beijing, China

5. Department of General Surgery, Capital Institute of Pediatrics Affiliated Children's Hospital, Beijing, China

Publisher

Impact Journals, LLC

Subject

Cell Biology,Ageing

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Association of rs2435357 and rs2506030 polymorphisms in RET with susceptibility to hirschsprung disease: A systematic review and meta-analysis;Frontiers in Pediatrics;2022-10-17

2. Emerging Roles of the α-Catenin Family Member α-Catulin in Development, Homeostasis and Cancer Progression;International Journal of Molecular Sciences;2022-10-08

3. Intrauterine exposure to oxidative stress induces caspase-1-dependent enteric nerve cell pyroptosis;Pediatric Surgery International;2022-08-22

4. Role of ARHGEF3 as a GEF and mTORC2 Regulator;Frontiers in Cell and Developmental Biology;2022-01-31

5. RET compound inheritance in Chinese patients with Hirschsprung disease: lack of penetrance from insufficient gene dysfunction;Human Genetics;2021-01-12

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