Xie X - Search Results

1

Significant Association of rs2147555 Genetic Polymorphism in the EDNRB Gene with Hirschsprung Disease in Southern Chinese Children.

Zheng Y, Lan C, Wang N, Xu X, Hu T, Wu Q, Xie X, Wang Z, Zhang Y, Li C. Zheng Y, et al. Among authors: xie x. Biomed Res Int. 2020 Oct 31;2020:5956412. doi: 10.1155/2020/5956412. eCollection 2020. Biomed Res Int. 2020. PMID: 33178831 Free PMC article.

2

Association of NRG1 and AUTS2 genetic polymorphisms with Hirschsprung disease in a South Chinese population.

Zhang Y, Xie X, Zeng J, Wu Q, Zhang R, Zhu D, Xia H. Zhang Y, et al. Among authors: xie x. J Cell Mol Med. 2018 Apr;22(4):2190-2199. doi: 10.1111/jcmm.13498. Epub 2018 Jan 29. J Cell Mol Med. 2018. PMID: 29377512 Free PMC article.

3

The intragenic epistatic association of ADD3 with biliary atresia in Southern Han Chinese population.

Wang Z, Xie X, Zhao J, Fu M, Li Y, Zhong W, Xia H, Zhang Y, Zhang RZ. Wang Z, et al. Among authors: xie x. Biosci Rep. 2018 Jun 12;38(3):BSR20171688. doi: 10.1042/BSR20171688. Print 2018 Jun 29. Biosci Rep. 2018. PMID: 29685956 Free PMC article.

4

Association of VAMP5 and MCC genetic polymorphisms with increased risk of Hirschsprung disease susceptibility in Southern Chinese children.

Zhao J, Xie X, Yao Y, He Q, Zhang R, Xia H, Zhang Y. Zhao J, et al. Among authors: xie x. Aging (Albany NY). 2018 Apr 25;10(4):689-700. doi: 10.18632/aging.101423. Aging (Albany NY). 2018. PMID: 29695640 Free PMC article.

5

Epistatic Association of CD14 and NOTCH2 Genetic Polymorphisms with Biliary Atresia in a Southern Chinese Population.

Lin Z, Xie X, Lin H, Fu M, Su L, Tong Y, Chen H, Wang H, Zhao J, Xia H, Zhang Y, Zhang R. Lin Z, et al. Among authors: xie x. Mol Ther Nucleic Acids. 2018 Dec 7;13:590-595. doi: 10.1016/j.omtn.2018.10.006. Epub 2018 Oct 16. Mol Ther Nucleic Acids. 2018. PMID: 30439647 Free PMC article.

6

Pleiotropic effect of common PHOX2B variants in Hirschsprung disease and neuroblastoma.

Zhao J, Zhu Y, Xie X, Yao Y, Zhang J, Zhang R, Huang L, Cheng J, Xia H, He J, Zhang Y. Zhao J, et al. Among authors: xie x. Aging (Albany NY). 2019 Feb 22;11(4):1252-1261. doi: 10.18632/aging.101834. Aging (Albany NY). 2019. PMID: 30799307 Free PMC article.

7

Associations of SLC6A20 genetic polymorphisms with Hirschsprung's disease in a Southern Chinese population.

Xie X, He Q, Huang L, Li L, Yao Y, Xia H, Zhao J, Zhong W, Zhang Y. Xie X, et al. Biosci Rep. 2019 Aug 13;39(8):BSR20182290. doi: 10.1042/BSR20182290. Print 2019 Aug 30. Biosci Rep. 2019. PMID: 31358688 Free PMC article. Clinical Trial.

8

miR-618 rs2682818 C>A polymorphism decreases Hirschsprung disease risk in Chinese children.

Zheng Y, Lu T, Xie X, He Q, Lu L, Zhong W. Zheng Y, et al. Among authors: xie x. Biosci Rep. 2020 May 29;40(5):BSR20193989. doi: 10.1042/BSR20193989. Biosci Rep. 2020. PMID: 32364585 Free PMC article.

9

Negative Association Between lncRNA HOTTIP rs3807598 C>G and Hirschsprung Disease.

Zheng Y, Zhuo Z, Xie X, Lu L, He Q, Zhong W. Zheng Y, et al. Among authors: xie x. Pharmgenomics Pers Med. 2020 May 6;13:151-156. doi: 10.2147/PGPM.S249649. eCollection 2020. Pharmgenomics Pers Med. 2020. PMID: 32440194 Free PMC article.

10

miR-100 rs1834306 A>G Increases the Risk of Hirschsprung Disease in Southern Chinese Children.

Zhu Y, Lin A, Zheng Y, Xie X, He Q, Zhong W. Zhu Y, et al. Among authors: xie x. Pharmgenomics Pers Med. 2020 Aug 10;13:283-288. doi: 10.2147/PGPM.S265730. eCollection 2020. Pharmgenomics Pers Med. 2020. PMID: 32848443 Free PMC article.

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