These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

80 related articles for article (PubMed ID: 29298094)

  • 1. A Rare Rs139365823 Polymorphism in Pre-miR-138 Is Associated with Risk of Congenital Heart Disease in a Chinese Population.
    Gao X; Yang L; Luo H; Tan F; Ma X; Lu C
    DNA Cell Biol; 2018 Feb; 37(2):109-116. PubMed ID: 29298094
    [TBL] [Abstract][Full Text] [Related]  

  • 2. No association of functional variant in pri-miR-218 and risk of congenital heart disease in a Chinese population.
    Gao X; Yang L; Ma Y; Yang J; Zhang G; Huang G; Huang Q; Chen L; Fu F; Chen Y; Su D; Dong Y; Ma X; Lu C; Peng X
    Gene; 2013 Jul; 523(2):173-7. PubMed ID: 23566829
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Single-nucleotide polymorphism of the pri-miR-34b/c gene is not associated with susceptibility to congenital heart disease in the Han Chinese population.
    Liu YM; Wang Y; Peng W; Wu Z; Wang XH; Wang ML; Wang W; Sun J; Zhang ZD; Mo XM
    Genet Mol Res; 2013 Aug; 12(3):2937-44. PubMed ID: 24065649
    [TBL] [Abstract][Full Text] [Related]  

  • 4. No association of pri-miR-143 rs41291957 polymorphism with the risk of congenital heart disease in a Chinese population.
    Yang L; Gao X; Luo H; Huang Q; Wei Y; Zhang G; Huang G; Su D; Chen L; Lu C; Yang J; Ma X
    Pediatr Cardiol; 2014 Aug; 35(6):1057-61. PubMed ID: 24752771
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Functional variant in microRNA-196a2 contributes to the susceptibility of congenital heart disease in a Chinese population.
    Xu J; Hu Z; Xu Z; Gu H; Yi L; Cao H; Chen J; Tian T; Liang J; Lin Y; Qiu W; Ma H; Shen H; Chen Y
    Hum Mutat; 2009 Aug; 30(8):1231-6. PubMed ID: 19514064
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Correlation between pri-miR-124 (rs531564) polymorphism and congenital heart disease susceptibility in Chinese population at two different altitudes: a case-control and in silico study.
    Yang W; Yi K; Yu H; Ding Y; Li D; Wei Y; You T; Xie X
    Environ Sci Pollut Res Int; 2019 Jul; 26(21):21983-21992. PubMed ID: 31144180
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association of functional variant in GDF1 promoter with risk of congenital heart disease and its regulation by Nkx2.5.
    Gao X; Zheng P; Yang L; Luo H; Zhang C; Qiu Y; Huang G; Sheng W; Ma X; Lu C
    Clin Sci (Lond); 2019 Jun; 133(12):1281-1295. PubMed ID: 31171573
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. APRISMA-compliant systematic review and meta-analysis determining the association of miRNA polymorphisms and risk of congenital heart disease.
    Li XY; Chen K; Lv ZT
    Medicine (Baltimore); 2019 Nov; 98(45):e17653. PubMed ID: 31702616
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Intronic Polymorphisms in Gene of Second Heart Field as Risk Factors for Human Congenital Heart Disease in a Chinese Population.
    Wang E; Nie Y; Fan X; Zheng Z; Hu S
    DNA Cell Biol; 2019 Jun; 38(6):521-531. PubMed ID: 31013439
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Germline hereditary, somatic mutations and microRNAs targeting-SNPs in congenital heart defects.
    Sabina S; Pulignani S; Rizzo M; Cresci M; Vecoli C; Foffa I; Ait-Ali L; Pitto L; Andreassi MG
    J Mol Cell Cardiol; 2013 Jul; 60():84-9. PubMed ID: 23583740
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Multiple gene variations contributed to congenital heart disease via GATA family transcriptional regulation.
    Qian Y; Xiao D; Guo X; Chen H; Hao L; Ma X; Huang G; Ma D; Wang H
    J Transl Med; 2017 Apr; 15(1):69. PubMed ID: 28372585
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association of a MiR-499 SNP and risk of congenital heart disease in a Chinese population.
    Guo R; Feng Z; Yang Y; Xu H; Zhang J; Guo K; Bi Y
    Cell Mol Biol (Noisy-le-grand); 2018 Jul; 64(10):108-112. PubMed ID: 30084801
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association Between
    Qi S; Wang C; Li L; Li T; Chen Q; Wang J
    Genet Test Mol Biomarkers; 2021 Dec; 25(12):735-740. PubMed ID: 34918978
    [No Abstract]   [Full Text] [Related]  

  • 16. The MALAT1 gene polymorphism and its relationship with the onset of congenital heart disease in Chinese.
    Li Q; Zhu W; Zhang B; Wu Y; Yan S; Yuan Y; Zhang H; Li J; Sun K; Wang H; Yu T
    Biosci Rep; 2018 May; 38(3):. PubMed ID: 29559566
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Association of TBX20 gene polymorphism with congenital heart disease in Han Chinese neonates.
    Chen J; Sun F; Fu J; Zhang H
    Pediatr Cardiol; 2015 Apr; 36(4):737-42. PubMed ID: 25487630
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Targeted next-generation sequencing identifies pathogenic variants in familial congenital heart disease.
    Blue GM; Kirk EP; Giannoulatou E; Dunwoodie SL; Ho JW; Hilton DC; White SM; Sholler GF; Harvey RP; Winlaw DS
    J Am Coll Cardiol; 2014 Dec; 64(23):2498-506. PubMed ID: 25500235
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 4.