174 related articles for article (PubMed ID: 25022354)
1. Common variations in BMP4 confer genetic susceptibility to sporadic congenital heart disease in a Han Chinese population.
Qian B; Mo R; Da M; Peng W; Hu Y; Mo X
Pediatr Cardiol; 2014 Dec; 35(8):1442-7. PubMed ID: 25022354
[TBL] [Abstract][Full Text] [Related]
2. Copy number variations in the GATA4, NKX2-5, TBX5, BMP4 CRELD1, and 22q11.2 gene regions in Chinese children with sporadic congenital heart disease.
Li Z; Huang J; Liang B; Zeng D; Luo S; Yan T; Liao F; Huang J; Li J; Cai R; Deng X; Tang N
J Clin Lab Anal; 2019 Feb; 33(2):e22660. PubMed ID: 30221396
[TBL] [Abstract][Full Text] [Related]
3. Genetic variants of the endothelial NO synthase gene (eNOS) may confer increased risk of sporadic congenital heart disease.
Zhou K; Wang Y; Peng W; Sun J; Qing YM; Mo XM
Genet Mol Res; 2014 May; 13(2):3805-11. PubMed ID: 24938467
[TBL] [Abstract][Full Text] [Related]
4. 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
Int J Clin Exp Pathol; 2015; 8(11):14917-24. PubMed ID: 26823822
[TBL] [Abstract][Full Text] [Related]
5. Replication of the 4p16 susceptibility locus in congenital heart disease in Han Chinese populations.
Zhao B; Lin Y; Xu J; Ni B; Da M; Ding C; Hu Y; Zhang K; Yang S; Wang X; Yu S; Chen Y; Mo X; Liu J; Shen H; Sha J; Ma H
PLoS One; 2014; 9(9):e107411. PubMed ID: 25215500
[TBL] [Abstract][Full Text] [Related]
6. Genetic variations of ISL1 associated with human congenital heart disease in Chinese Han people.
Luo ZL; Sun H; Yang ZQ; Ma YH; Gu Y; He YQ; Wei D; Xia LB; Yang BH; Guo T
Genet Mol Res; 2014 Feb; 13(1):1329-38. PubMed ID: 24634231
[TBL] [Abstract][Full Text] [Related]
7. Characterization of human bone morphogenetic protein gene variants for possible roles in congenital heart disease.
Li FF; Deng X; Zhou J; Yan P; Zhao EY; Liu SL
Mol Med Rep; 2016 Aug; 14(2):1459-64. PubMed ID: 27357418
[TBL] [Abstract][Full Text] [Related]
8. Association of two variants in SMAD7 with the risk of congenital heart disease in the Han Chinese population.
Wang E; Jin W; Duan W; Qiao B; Sun S; Huang G; Shi K; Jin L; Wang H
PLoS One; 2013; 8(9):e72423. PubMed ID: 24039762
[TBL] [Abstract][Full Text] [Related]
9. Susceptibility to congenital heart defects associated with a polymorphism in TBX2 3' untranslated region in the Han Chinese population.
Wang J; Zhang RR; Cai K; Yang Q; Duan WY; Zhao JY; Gui YH; Wang F
Pediatr Res; 2019 Feb; 85(3):378-383. PubMed ID: 30262811
[TBL] [Abstract][Full Text] [Related]
10. Association of aminoacyl-tRNA synthetases gene polymorphisms with the risk of congenital heart disease in the Chinese Han population.
Da M; Feng Y; Xu J; Hu Y; Lin Y; Ni B; Qian B; Hu Z; Mo X
PLoS One; 2014; 9(10):e110072. PubMed ID: 25310850
[TBL] [Abstract][Full Text] [Related]
11. Lower Circulating Folate Induced by a Fidgetin Intronic Variant Is Associated With Reduced Congenital Heart Disease Susceptibility.
Wang D; Wang F; Shi KH; Tao H; Li Y; Zhao R; Lu H; Duan W; Qiao B; Zhao SM; Wang H; Zhao JY
Circulation; 2017 May; 135(18):1733-1748. PubMed ID: 28302752
[TBL] [Abstract][Full Text] [Related]
12. Associations between IL-6 Variations and Congenital Heart Disease Incidence among Chinese Han People.
Zhang Q; Wang H; Xue J; Wu D
Med Sci Monit; 2020 Jun; 26():e921032. PubMed ID: 32519679
[TBL] [Abstract][Full Text] [Related]
13. Association between polymorphisms in IL27 and risk for CHD in a Chinese population.
Zhang D; Ma M; Yang Y; Wan L; Yang Z; Lv J; Li X; Yang H; Huang P; Li L
Cardiol Young; 2016 Feb; 26(2):237-43. PubMed ID: 25662568
[TBL] [Abstract][Full Text] [Related]
14. ISL1 common variant rs1017 is not associated with susceptibility to congenital heart disease in a Chinese population.
Xue L; Wang X; Xu J; Xu X; Liu X; Hu Z; Shen H; Chen Y
Genet Test Mol Biomarkers; 2012 Jul; 16(7):679-83. PubMed ID: 22480195
[TBL] [Abstract][Full Text] [Related]
15. Genetic analysis of BMP4 gene in Chinese Han female population with premature ovarian insufficiency.
Bai T; Yang J; Chen B; Wang B; Ma X; Cao Y
Climacteric; 2014 Jun; 17(3):304-6. PubMed ID: 24559233
[TBL] [Abstract][Full Text] [Related]
16. Characterization of soluble N-ethylmaleimide-sensitive factor attachment protein receptor gene STX18 variations for possible roles in congenital heart diseases.
Li X; Shi S; Li FF; Cheng R; Han Y; Diao LW; Zhang Q; Zhi JX; Liu SL
Gene; 2017 Jan; 598():79-83. PubMed ID: 27816473
[TBL] [Abstract][Full Text] [Related]
17. 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
Gene; 2016 Jan; 575(1):29-33. PubMed ID: 26297999
[TBL] [Abstract][Full Text] [Related]
18. [Association between rs6658835 polymorphism of transforming growth factor beta 2 gene and congenital heart diseases in Chinese Han population].
Xie J; Chen Y; Li H; Zhou B; Rao L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Apr; 29(2):210-3. PubMed ID: 22487836
[TBL] [Abstract][Full Text] [Related]
19. Association of genetic polymorphisms of de novo nucleotide biosynthesis with increased CHD susceptibility in the northern Chinese population.
Jiang YC; Kuang LL; Sun SN; Duan WY; Qiao B; Wang HY
Clin Genet; 2017 May; 91(5):748-755. PubMed ID: 27659940
[TBL] [Abstract][Full Text] [Related]
20. T allele at site 6007 of bone morphogenetic protein-4 gene increases genetic susceptibility to ossification of the posterior longitudinal ligament in male Chinese Han population.
Meng XL; Wang H; Yang H; Hai Y; Tian BP; Lin X
Chin Med J (Engl); 2010 Sep; 123(18):2537-42. PubMed ID: 21034624
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
