131 related articles for article (PubMed ID: 30629480)
1. NOTCH1 Gene MicroRNA Target Variation and Ventricular Septal Defect Risk.
Ji L; Hou H; Zhu K; Liu X; Liu Y; Wang Q; Li J; Liu H; Zhang Q; Lv J; Alexander R; Wang W; Li D
OMICS; 2019 Jan; 23(1):28-35. PubMed ID: 30629480
[TBL] [Abstract][Full Text] [Related]
2. Association of DARS gene polymorphisms with the risk of isolated ventricular septal defects in the Chinese Han population.
Feng Y; Chen R; Mo X
Ital J Pediatr; 2016 Nov; 42(1):102. PubMed ID: 27871331
[TBL] [Abstract][Full Text] [Related]
3. Genetic analysis of the CITED2 gene promoter in isolated and sporadic congenital ventricular septal defects.
Zheng SQ; Chen HX; Liu XC; Yang Q; He GW
J Cell Mol Med; 2021 Feb; 25(4):2254-2261. PubMed ID: 33439552
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. VEGF C-634G polymorphism is associated with protection from isolated ventricular septal defect: case-control and TDT studies.
Xie J; Yi L; Xu ZF; Mo XM; Hu YL; Wang DJ; Ren HZ; Han B; Wang Y; Yang C; Zhao YL; Shi DQ; Jiang YZ; Shen L; Qiao D; Chen SL; Yu BJ
Eur J Hum Genet; 2007 Dec; 15(12):1246-51. PubMed ID: 17625508
[TBL] [Abstract][Full Text] [Related]
6. Presenilin-1 polymorphisms are not relevant in susceptibility to ventricular septal defect: a case-control study.
Chen Y; Li H; Zhou B; Peng Y; Zheng Q; Rao L
DNA Cell Biol; 2011 Aug; 30(8):565-8. PubMed ID: 21323574
[TBL] [Abstract][Full Text] [Related]
7. First report of polymorphisms in MTRR, GATA4, VEGF, and ISL1 genes in Pakistani children with isolated ventricular septal defects (VSD).
Sarwar S; Ehsan F; Shabana ; Tahir A; Jamil M; Shahid SU; Khan A; Hasnain S
Ital J Pediatr; 2021 Mar; 47(1):70. PubMed ID: 33757570
[TBL] [Abstract][Full Text] [Related]
8. Analysis of RTN4 3'UTR insertion/deletion polymorphisms in ventricular septal defect in a Chinese Han population.
Chen Y; Zhou B; Li H; Peng Y; Wang Y; Rao L
DNA Cell Biol; 2011 May; 30(5):323-7. PubMed ID: 21166502
[TBL] [Abstract][Full Text] [Related]
9. A miRNA-binding-site SNP of MSX1 is Associated with NSOC Susceptibility.
Ma L; Xu M; Li D; Han Y; Wang Z; Yuan H; Ma J; Zhang W; Jiang H; Pan Y; Wang L
J Dent Res; 2014 Jun; 93(6):559-64. PubMed ID: 24603642
[TBL] [Abstract][Full Text] [Related]
10. Characterization of circulating microRNA expression in patients with a ventricular septal defect.
Li D; Ji L; Liu L; Liu Y; Hou H; Yu K; Sun Q; Zhao Z
PLoS One; 2014; 9(8):e106318. PubMed ID: 25165856
[TBL] [Abstract][Full Text] [Related]
11. Polymorphisms in microRNA target sites modulate risk of lymphoblastic and myeloid leukemias and affect microRNA binding.
Dzikiewicz-Krawczyk A; Macieja A; Mały E; Januszkiewicz-Lewandowska D; Mosor M; Fichna M; Strauss E; Nowak J
J Hematol Oncol; 2014 Jun; 7():43. PubMed ID: 24886876
[TBL] [Abstract][Full Text] [Related]
12. Functional Polymorphism Located in the microRNA Binding Site of the Insulin Receptor (INSR) Gene Confers Risk for Type 2 Diabetes Mellitus in the Bangladeshi Population.
Parvin M; Jahan F; Sarkar PK; Howlader ZH; Nabi AHMN; Hosen MI
Biochem Genet; 2019 Feb; 57(1):20-33. PubMed ID: 29971619
[TBL] [Abstract][Full Text] [Related]
13. 3'UTR SNPs and Haplotypes in the GATA4 Gene Contribute to the Genetic Risk of Congenital Heart Disease.
Pulignani S; Vecoli C; Sabina S; Foffa I; Ait-Ali L; Andreassi MG
Rev Esp Cardiol (Engl Ed); 2016 Aug; 69(8):760-5. PubMed ID: 27118528
[TBL] [Abstract][Full Text] [Related]
14. Association of NFATc1 gene polymorphism with ventricular septal defect in the Chinese Han population.
Shen L; Li ZZ; Shen AD; Liu H; Bai S; Guo J; Yuan F; Li XF
Chin Med J (Engl); 2013 Jan; 126(1):78-81. PubMed ID: 23286482
[TBL] [Abstract][Full Text] [Related]
15. Novel and functional DNA sequence variants within the GATA5 gene promoter in ventricular septal defects.
Shan JP; Wang XL; Qiao YG; Wan Yan HX; Huang WH; Pang SC; Yan B
World J Pediatr; 2014 Nov; 10(4):348-53. PubMed ID: 25515806
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Identification of variants of
Zheng SQ; Chen HX; Liu XC; Yang Q; He GW
Am J Physiol Cell Physiol; 2021 Sep; 321(3):C443-C452. PubMed ID: 34260301
[TBL] [Abstract][Full Text] [Related]
18. Polymorphisms in lipid metabolism related miRNA binding sites and risk of metabolic syndrome.
Ye Q; Zhao X; Xu K; Li Q; Cheng J; Gao Y; Du J; Shi H; Zhou L
Gene; 2013 Oct; 528(2):132-8. PubMed ID: 23911300
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. A novel GATA6 mutation associated with congenital ventricular septal defect.
Zheng GF; Wei D; Zhao H; Zhou N; Yang YQ; Liu XY
Int J Mol Med; 2012 Jun; 29(6):1065-71. PubMed ID: 22407241
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
