BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 22487836)

  • 1. [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]  

  • 2. Genetic variance of transforming growth factor β2 gene in conotruncal heart defects.
    Chen Y; Zhang R; Xie J; Li Y; Shi S; Qian H; Yan Z; Rao L
    Biomarkers; 2017; 22(3-4):287-290. PubMed ID: 27564654
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association between TGFBR2 gene polymorphisms and congenital heart defects in Han Chinese population.
    Huang F; Li L; Shen C; Wang H; Chen J; Chen W; Chen X
    Nutr Hosp; 2014 Oct; 31(2):710-5. PubMed ID: 25617554
    [TBL] [Abstract][Full Text] [Related]  

  • 4. MTHFR C677T and A1298C gene polymorphisms and their relation to homocysteine level in Egyptian children with congenital heart diseases.
    Zidan HE; Rezk NA; Mohammed D
    Gene; 2013 Oct; 529(1):119-24. PubMed ID: 23933414
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Absence of association between length variation of an intronic region in the NFATC1 gene and congenital heart defects in a Han Chinese population.
    Liu H; Dai L; Mao M; Wang X; Hua Y; Xie L
    DNA Cell Biol; 2012 Jan; 31(1):88-91. PubMed ID: 22032245
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The NFKB1 -94 ATTG insertion/deletion polymorphism (rs28362491) contributes to the susceptibility of congenital heart disease in a Chinese population.
    Zhang D; Li L; Zhu Y; Zhao L; Wan L; Lv J; Li X; Huang P; Wei L; Ma M
    Gene; 2013 Mar; 516(2):307-10. PubMed ID: 23299027
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association of miR-196a2, miR-27a, and miR-499 polymorphisms with isolated congenital heart disease in a Chinese population.
    Yu K; Ji Y; Wang H; Xuan QK; Li BB; Xiao JJ; Sun W; Kong XQ
    Genet Mol Res; 2016 Oct; 15(4):. PubMed ID: 27813602
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Association of 22q11 deletion with isolated congenital heart disease in three Chinese ethnic groups.
    Jiang L; Duan C; Chen B; Hou Z; Chen Z; Li Y; Huan Y; Wu KK
    Int J Cardiol; 2005 Nov; 105(2):216-23. PubMed ID: 16243116
    [TBL] [Abstract][Full Text] [Related]  

  • 10. TCF21 rs12190287 Polymorphisms Are Associated with Ventricular Septal Defects in a Chinese Population.
    Yang L; Gao X; Luo H; Huang Q; Su D; Tan X; Lu C
    Genet Test Mol Biomarkers; 2017 May; 21(5):312-315. PubMed ID: 28346832
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 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. 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]  

  • 14. Association of NKX2-5, GATA4, and TBX5 polymorphisms with congenital heart disease in Egyptian children.
    Behiry EG; Al-Azzouny MA; Sabry D; Behairy OG; Salem NE
    Mol Genet Genomic Med; 2019 May; 7(5):e612. PubMed ID: 30834692
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Maternal and offspring MTHFR gene C677T polymorphism as predictors of congenital atrial septal defect and patent ductus arteriosus.
    Zhu WL; Li Y; Yan L; Dao J; Li S
    Mol Hum Reprod; 2006 Jan; 12(1):51-4. PubMed ID: 16373366
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population.
    An Y; Duan W; Huang G; Chen X; Li L; Nie C; Hou J; Gui Y; Wu Y; Zhang F; Shen Y; Wu B; Wang H
    BMC Med Genomics; 2016 Jan; 9():2. PubMed ID: 26742958
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.