Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Chaoting Lan"'
Autor:
Weiyong Zhong, Chaoting Lan, Yuqiong Chen, Kai Song, Zuyi Ma, Jixiao Zeng, Lihua Huang, Yan Zhang, Yun Zhu, Huimin Xia
Publikováno v:
Journal of Immunology Research, Vol 2024 (2024)
Conclusion: This study suggested that virus-triggered autoimmunity may contribute to HSCR through activation of innate immunity, which facilitates the diagnosis and prevention of HSCR.
Externí odkaz:
https://doaj.org/article/7188030f6d604a58b0fda5816c788dd5
Autor:
Chaoting Lan, Yanqing Liu, Xiao Wu, Bingtong Wang, Songqing Xin, Qiuming He, Wei Zhong, Zipeng Liu
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundHirschsprung's disease (HSCR) is currently considered to be a congenital gastrointestinal malformation caused mainly by genetic factors. Endothelin Converting Enzyme-1 (ECE1) has been reported to be associated with HSCR. However, the relati
Externí odkaz:
https://doaj.org/article/d96d83681fe04379b727e5c9deeade29
Autor:
Bingtong Wang, Yongxuan Yao, Wenlin Fang, Yanqing Liu, Wei Zhong, Ye He, Yulu Lai, Qiuming He, Yun Zhu, Chaoting Lan
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
BackgroundHirschsprung’s disease (HSCR) is a neonatal enteric nervous system (ENS) disease characterized by congenital enteric ganglion cell loss. The only treatment is aganglionic bowel segment resection and innervated bowel segment reconstruction
Externí odkaz:
https://doaj.org/article/82dcdc9a26df416f8da3a989121c755e
Publikováno v:
Clinical and Experimental Gastroenterology.
Bingtong Wang,* Wenlin Fang,* Dingjiang Qin,* Qiuming He, Chaoting Lan Guangzhou Women and Childrenâs Medical Center, Guangzhou Medical University, Guangdong Provincial Clinical Research Center for Child Health, Guangzhou, 510623, Pe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b72cff2296e2d79f6ce316b955d1adc3
https://www.dovepress.com/susceptibility-of-pcsk2-polymorphism-to-hirschsprung-disease-in-southe-peer-reviewed-fulltext-article-CEG
https://www.dovepress.com/susceptibility-of-pcsk2-polymorphism-to-hirschsprung-disease-in-southe-peer-reviewed-fulltext-article-CEG
Autor:
Chaoting, Lan, Yanqing, Liu, Xiao, Wu, Bingtong, Wang, Songqing, Xin, Qiuming, He, Wei, Zhong, Zipeng, Liu
Publikováno v:
Frontiers in pediatrics. 10
Hirschsprung's disease (HSCR) is currently considered to be a congenital gastrointestinal malformation caused mainly by genetic factors. Endothelin Converting Enzyme-1 (1,470 HSCR patients and 1,473 controls from a southern Chinese population were re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::52f652b3a783f435c7690f72bca148d8
https://pubmed.ncbi.nlm.nih.gov/36619519
https://pubmed.ncbi.nlm.nih.gov/36619519
Publikováno v:
Transl Pediatr
BACKGROUND: Hirschsprung’s disease (HSCR) is a rare congenital disease in which enteric nervous system (ENS) in the distal intestine is absent. HSCR is a disease involving genetic factors and environmental factors. Despite a series of genes have be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0e5dedf5fdff3768a481284f789fcad
https://europepmc.org/articles/PMC9253937/
https://europepmc.org/articles/PMC9253937/
Autor:
Yanqing Liu, Bingxiao Li, Yuxin Wu, Xiaoyu Zuo, Ning Wang, Lihua Huang, Chaoting Lan, Yun Zhu
Publikováno v:
Journal of Clinical Laboratory Analysis
Background Hirschsprung’s disease (HSCR) is an enteric nervous system birth defect partially caused by a genetic disorder. Single‐nucleotide polymorphisms (SNPs) of the cytochrome P450 family 2 subfamily B member 6 (CYP2B6) gene are reported to b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2802f1d1660a9be1b3db94203b078bb
http://europepmc.org/articles/PMC8649360
http://europepmc.org/articles/PMC8649360
Autor:
Yun Luo, Yuxin Wu, Lifeng Lu, Huimin Xia, Chaoting Lan, Wei Zhong, Jixiao Zeng, Yi Zheng, Yan Zhang, Lihua Huang, Yun Zhu, Jinglu Zhao, Ning Wang
Publikováno v:
Journal of Cellular and Molecular Medicine
Hirschsprung disease (HSCR) is an infrequent congenital intestinal dysplasia. The known genetic variations are unable to fully explain the pathogenesis of HSCR. The α/β‐hydratase domain 1 (ABHD1) interferes with the proliferation and migration of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac3fa7ce6e3ed02eec336d053d16586d
https://pubmed.ncbi.nlm.nih.gov/34545688
https://pubmed.ncbi.nlm.nih.gov/34545688
Autor:
Yi, Zheng, ChaoTing, Lan, Ning, Wang, Xiaogang, Xu, Tuqun, Hu, Qi, Wu, Xiaoli, Xie, Zhe, Wang, Yan, Zhang, Cong, Li
Publikováno v:
BioMed Research International
Hirschsprung disease (HSCR) is a human birth defect at the clinical setting, usually characterized by an absent enteric nervous system (ENS) from the distal bowel. The majority of HSCR cases represent a complex disorder resulting from the interaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::340618ecbdbaf3dec153b42f59cdc86f
https://pubmed.ncbi.nlm.nih.gov/33178831
https://pubmed.ncbi.nlm.nih.gov/33178831
Autor:
Cong Li, Xiaoli Xie, Qi Wu, Xiaogang Xu, Yi Zheng, Zhe Wang, Yan Zhang, Tuqun Hu, ChaoTing Lan, Ning Wang
Publikováno v:
BioMed Research International, Vol 2020 (2020)
Hirschsprung disease (HSCR) is a human birth defect at the clinical setting, usually characterized by an absent enteric nervous system (ENS) from the distal bowel. The majority of HSCR cases represent a complex disorder resulting from the interaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d995e73a52a582e97f8052b35cf8f6b7
https://doaj.org/article/9fdadeff279c41509e2a7ab327754448
https://doaj.org/article/9fdadeff279c41509e2a7ab327754448