120 related articles for article (PubMed ID: 33026847)
21. Association of WNT Pathway Genes With Nonsyndromic Cleft Lip With or Without Cleft Palate.
Vijayan V; Ummer R; Weber R; Silva R; Letra A
Cleft Palate Craniofac J; 2018 Mar; 55(3):335-341. PubMed ID: 29437498
[TBL] [Abstract][Full Text] [Related]
22. Pathway Analyses Identify Novel Variants in the WNT Signaling Pathway Associated with Tuberculosis in Chinese Population.
Hu X; Zhou J; Chen X; Zhou Y; Song X; Cai B; Zhang J; Lu X; Ying B
Sci Rep; 2016 Jun; 6():28530. PubMed ID: 27334567
[TBL] [Abstract][Full Text] [Related]
23. Association of genetic variations in the Wnt signaling pathway genes with myocardial infarction susceptibility in Chinese Han population.
Tao J; Wang YT; Abudoukelimu M; Yang YN; Li XM; Xie X; Chen BD; Liu F; He CH; Li HY; Ma YT
Oncotarget; 2016 Aug; 7(33):52740-52750. PubMed ID: 27391264
[TBL] [Abstract][Full Text] [Related]
24. The haplotypes of TNFRSF17 polymorphisms are associated with colon cancer in a Korean population.
Chae SC; Yu JI; Uhm TB; Lee SY; Kang DB; Lee JK; Park WC; Yun KJ
Int J Colorectal Dis; 2012 Jun; 27(6):701-7. PubMed ID: 22108903
[TBL] [Abstract][Full Text] [Related]
25. Haplotype-based association of renin gene polymorphisms with essential hypertension in Han population of northern china.
Zhang G; Li X; Zhang K; Zhao J; Qiu C
J Renin Angiotensin Aldosterone Syst; 2017; 18(4):1470320317744917. PubMed ID: 29233044
[TBL] [Abstract][Full Text] [Related]
26. Risk of Wnt/β-catenin signalling pathway gene polymorphisms in primary Sjögren's syndrome.
Fernández-Torres J; Pérez-Hernández N; Hernández-Molina G; Martínez-Nava GA; Garrido-Rodríguez D; López-Reyes A; Rodríguez-Pérez JM
Rheumatology (Oxford); 2020 Feb; 59(2):418-425. PubMed ID: 31302686
[TBL] [Abstract][Full Text] [Related]
27. [A related analysis for alpha, beta fibrinogen gene haplotypes and nucleotide polymorphisms associated with the ischemic stroke in Hainan Han population].
Liang L; Sun C; Liao XP; Xiao F; Chen XD; Huang SX; Tang XL; Wen GQ; Long ZG; Wang XY; Liu GX; Cheng S; Cai WW
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun; 23(3):316-9. PubMed ID: 16767673
[TBL] [Abstract][Full Text] [Related]
28. Genetic Polymorphisms in APC, DVL2, and AXIN1 Are Associated with Susceptibility, Advanced TNM Stage or Tumor Location in Colorectal Cancer.
Rosales-Reynoso MA; Saucedo-Sariñana AM; Contreras-Díaz KB; Márquez-González RM; Barros-Núñez P; Pineda-Razo TD; Marin-Contreras ME; Durán-Anguiano Ó; Gallegos-Arreola MP; Flores-Martínez SE; Sánchez-Corona J
Tohoku J Exp Med; 2019 Nov; 249(3):173-183. PubMed ID: 31723073
[TBL] [Abstract][Full Text] [Related]
29. [Association of Crohn's disease with aryl hydrocarbon receptor gene polymorphisms and haplotypes].
Wu CQ; Cao SG; Xia XP; Xu CL; Xia SL; Lin XQ; Jin J; Ding R; Jiang Y
Zhonghua Nei Ke Za Zhi; 2018 Jan; 57(1):37-43. PubMed ID: 29325309
[No Abstract] [Full Text] [Related]
30. Genetic polymorphisms of RAGE and risk of ulcerative colitis in a Chinese population.
Wang J; Zeng J; Wang H; Ye S; Bi Y; Zhou Y; Li K; Zhou Y
Immunol Lett; 2016 Feb; 170():88-94. PubMed ID: 26349055
[TBL] [Abstract][Full Text] [Related]
31. Association between Single-nucleotide Polymorphisms of RXRG and Genetic Susceptibility to Type 2 Diabetes in South China.
Yu H; Wang S; Hu W; Xu L; Ding Y; Kong D; Pan H
Curr Mol Med; 2020; 20(6):408-414. PubMed ID: 31808386
[TBL] [Abstract][Full Text] [Related]
32. Association between
Gao M; Zeng K; Li Y; Liu YP; Xia X; Xu FL; Yao J; Wang BJ
J Int Med Res; 2020 Jun; 48(6):300060520932801. PubMed ID: 32567430
[TBL] [Abstract][Full Text] [Related]
33. Association Between ADRB2 Genetic Polymorphisms and the Risk of Chronic Obstructive Pulmonary Disease: A Case-Control Study in a Chinese Population.
Zhao H; Wu X; Dong CL; Wang BY; Zhao J; Cao XE
Genet Test Mol Biomarkers; 2017 Aug; 21(8):491-496. PubMed ID: 28753063
[TBL] [Abstract][Full Text] [Related]
34. The -137G/C single nucleotide polymorphism in IL-18 gene promoter contributes to tuberculosis susceptibility in Chinese Han population.
Zhou C; Ouyang N; Li QH; Luo SX; He Q; Lei H; Liu Q
Infect Genet Evol; 2015 Dec; 36():376-380. PubMed ID: 26474654
[TBL] [Abstract][Full Text] [Related]
35. Inhibition of the immunoproteasome LMP2 ameliorates ischemia/hypoxia-induced blood-brain barrier injury through the Wnt/β-catenin signalling pathway.
Chen XY; Wan SF; Yao NN; Lin ZJ; Mao YG; Yu XH; Wang YZ
Mil Med Res; 2021 Dec; 8(1):62. PubMed ID: 34857032
[TBL] [Abstract][Full Text] [Related]
36. Evaluation of Common Variants in the
Zhao T; Ma C; Xie B; Zhao B; Wang W; Liu J
Genet Test Mol Biomarkers; 2020 Jul; 24(7):425-430. PubMed ID: 32460535
[No Abstract] [Full Text] [Related]
37. The axis inhibition protein 2 polymorphisms and non-syndromic orofacial clefts susceptibility in a Chinese Han population.
Han Y; Zhou L; Ma L; Li D; Xu M; Yuan H; Ma J; Zhang W; Jiang H; Wu Y; Wang L; Pan Y
J Oral Pathol Med; 2014 Aug; 43(7):554-60. PubMed ID: 24484320
[TBL] [Abstract][Full Text] [Related]
38. Association between DNA methyltransferases 3B gene polymorphisms and the susceptibility to acute myeloid leukemia in Chinese Han population.
Zheng Q; Zeng TT; Chen J; Liu H; Zhang H; Su J
PLoS One; 2013; 8(9):e74626. PubMed ID: 24069326
[TBL] [Abstract][Full Text] [Related]
39. Endothelial Wnt/β-catenin signaling reduces immune cell infiltration in multiple sclerosis.
Lengfeld JE; Lutz SE; Smith JR; Diaconu C; Scott C; Kofman SB; Choi C; Walsh CM; Raine CS; Agalliu I; Agalliu D
Proc Natl Acad Sci U S A; 2017 Feb; 114(7):E1168-E1177. PubMed ID: 28137846
[TBL] [Abstract][Full Text] [Related]
40. Single Nucleotide Polymorphisms in the PTPN1 Gene Are Associated with Susceptibility to Esophageal Squamous Cell Carcinoma: A Case-Control Study in Inner Mongolia, China.
Ji HB; Wang LL; Wang XY; Yin SJ; Shang D; Sun LL; Wang L
Genet Test Mol Biomarkers; 2017 May; 21(5):305-311. PubMed ID: 28287835
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
