Wei C - Search Results

1

Lack of association of TLR4 gene Asp299Gly and Thr399Ile polymorphisms with rheumatoid arthritis in Chinese Han population of Yunnan Province.

Zheng B, Li Q, Wei C, Qin J, Shou T, Zhou R, Shao J, Yang Y, Xiao C. Zheng B, et al. Among authors: wei c. Rheumatol Int. 2010 Jul;30(9):1249-52. doi: 10.1007/s00296-010-1400-y. Epub 2010 Mar 20. Rheumatol Int. 2010. PMID: 20306049

2

Association of TLR4 gene non-missense single nucleotide polymorphisms with rheumatoid arthritis in Chinese Han population.

Yang H, Wei C, Li Q, Shou T, Yang Y, Xiao C, Yu M, Li M, Yang Z, Zhang J, Zheng B. Yang H, et al. Among authors: wei c. Rheumatol Int. 2013 May;33(5):1283-8. doi: 10.1007/s00296-012-2536-8. Epub 2012 Nov 6. Rheumatol Int. 2013. PMID: 23129427

3

The prognostic value of p53 expression for patients with cervical cancer: a meta analysis.

Zhou R, Wei C, Liu J, Luo Y, Tang W. Zhou R, et al. Among authors: wei c. Eur J Obstet Gynecol Reprod Biol. 2015 Dec;195:210-213. doi: 10.1016/j.ejogrb.2015.10.006. Epub 2015 Oct 23. Eur J Obstet Gynecol Reprod Biol. 2015. PMID: 26595307

4

Interaction between hypertension and HSP70 variants increase the risk of cerebral ischemia in Chinese Han population: an association study.

Wei Y, Wang W, He Y, Jiang L, Hou Z, Gao X, Wei C, Cen M, Yang L, Tan A, Yang W, Wang Y, Jin X. Wei Y, et al. Among authors: wei c. Gene. 2013 Jan 25;513(2):239-43. doi: 10.1016/j.gene.2012.11.002. Epub 2012 Nov 12. Gene. 2013. PMID: 23154057

5

Mouse models in modeling aging and cancer.

Li H, Wei C, Zhou R, Wang B, Zhang Y, Shao C, Luo Y. Li H, et al. Among authors: wei c. Exp Gerontol. 2019 Jun;120:88-94. doi: 10.1016/j.exger.2019.03.002. Epub 2019 Mar 12. Exp Gerontol. 2019. PMID: 30876950 Review.

6

The triggers of the cGAS-STING pathway and the connection with inflammatory and autoimmune diseases.

Zhou R, Xie X, Li X, Qin Z, Wei C, Liu J, Luo Y. Zhou R, et al. Among authors: wei c. Infect Genet Evol. 2020 Jan;77:104094. doi: 10.1016/j.meegid.2019.104094. Epub 2019 Nov 2. Infect Genet Evol. 2020. PMID: 31689545 Free article. Review.

7

Genetic variations of NKX2-5 in sporadic atrial septal defect and ventricular septal defect in Chinese Yunnan population.

Cao Y, Wang J, Wei C, Hou Z, Li Y, Zou H, Meng M, Wang W, Jiang L. Cao Y, et al. Among authors: wei c. Gene. 2016 Jan 1;575(1):29-33. doi: 10.1016/j.gene.2015.08.033. Epub 2015 Aug 20. Gene. 2016. PMID: 26297999 Clinical Trial.

8

Single nucleotide polymorphism of NKX2-5 gene with sporadic congenital heart disease in Chinese Bai population.

Cao Y, Lan W, Li Y, Wei C, Zou H, Jiang L. Cao Y, et al. Among authors: wei c. Int J Clin Exp Pathol. 2015 Nov 1;8(11):14917-24. eCollection 2015. Int J Clin Exp Pathol. 2015. PMID: 26823822 Free PMC article.

9

Interactions between angiotensin-converting enzyme-2 polymorphisms and high salt intake increase the risk of hypertension in the Chinese Wa population.

He Y, Yang W, Liu S, Gan L, Zhang F, Mu C, Wang J, Qu L, Wang R, Deng J, Ye Q, Yang X, Dong Y, Wang Q, Wei C, Hou Z, Yang L. He Y, et al. Among authors: wei c. Int J Clin Exp Pathol. 2017 Nov 1;10(11):11159-11168. eCollection 2017. Int J Clin Exp Pathol. 2017. PMID: 31966466 Free PMC article.

10

Association between 5, 10-methylenetetrahydrofolate reductase (MTHFR) polymorphisms and congenital heart disease: A meta-analysis.

Wang W, Hou Z, Wang C, Wei C, Li Y, Jiang L. Wang W, et al. Among authors: wei c. Meta Gene. 2013 Oct 28;1:109-25. doi: 10.1016/j.mgene.2013.09.009. eCollection 2013 Dec. Meta Gene. 2013. PMID: 25606381 Free PMC article.

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