164 related articles for article (PubMed ID: 31013439)
1. 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]
2. Minor alleles of genetic variants in second heart field increase the risk of hypoplastic right heart syndrome.
Wang E; Nie Y; Fan X; Zheng Z; Gu H; Zhang H; Hu S
J Genet; 2019 Jun; 98(2):. PubMed ID: 31204705
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. ISL1 directly regulates FGF10 transcription during human cardiac outflow formation.
Golzio C; Havis E; Daubas P; Nuel G; Babarit C; Munnich A; Vekemans M; Zaffran S; Lyonnet S; Etchevers HC
PLoS One; 2012; 7(1):e30677. PubMed ID: 22303449
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. [Association of single nucleotide polymorphisms of transcription factors with congenital heart diseases in the Chinese population: a Meta analysis].
Chen LT; Yang TB; Wang TT; Zheng Z; Zhao LJ; Ye ZW; Zhang SM; Qin JB
Zhongguo Dang Dai Er Ke Za Zhi; 2018 Jun; 20(6):490-496. PubMed ID: 29972125
[TBL] [Abstract][Full Text] [Related]
8. A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect.
Lin X; Huo Z; Liu X; Zhang Y; Li L; Zhao H; Yan B; Liu Y; Yang Y; Chen YH
J Hum Genet; 2010 Oct; 55(10):662-7. PubMed ID: 20631719
[TBL] [Abstract][Full Text] [Related]
9. TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus.
Huang RT; Wang J; Xue S; Qiu XB; Shi HY; Li RG; Qu XK; Yang XX; Liu H; Li N; Li YJ; Xu YJ; Yang YQ
Int J Med Sci; 2017; 14(4):323-332. PubMed ID: 28553164
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Novel GATA6 mutations associated with congenital ventricular septal defect or tetralogy of fallot.
Wang J; Luo XJ; Xin YF; Liu Y; Liu ZM; Wang Q; Li RG; Fang WY; Wang XZ; Yang YQ
DNA Cell Biol; 2012 Nov; 31(11):1610-7. PubMed ID: 23020118
[TBL] [Abstract][Full Text] [Related]
12. Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease.
LaHaye S; Corsmeier D; Basu M; Bowman JL; Fitzgerald-Butt S; Zender G; Bosse K; McBride KL; White P; Garg V
Circ Cardiovasc Genet; 2016 Aug; 9(4):320-9. PubMed ID: 27418595
[TBL] [Abstract][Full Text] [Related]
13. Single-Nucleotide Polymorphisms in Exonic and Promoter Regions of Transcription Factors of Second Heart Field Associated with Sporadic Congenital Cardiac Anomalies.
Wang E; Fan X; Nie Y; Zheng Z; Hu S
Balkan J Med Genet; 2021 Nov; 24(2):39-47. PubMed ID: 36249516
[TBL] [Abstract][Full Text] [Related]
14. Interaction of Gata4 and Gata6 with Tbx5 is critical for normal cardiac development.
Maitra M; Schluterman MK; Nichols HA; Richardson JA; Lo CW; Srivastava D; Garg V
Dev Biol; 2009 Feb; 326(2):368-77. PubMed ID: 19084512
[TBL] [Abstract][Full Text] [Related]
15. Genetic analysis of essential cardiac transcription factors in 256 patients with non-syndromic congenital heart defects.
Kodo K; Nishizawa T; Furutani M; Arai S; Ishihara K; Oda M; Makino S; Fukuda K; Takahashi T; Matsuoka R; Nakanishi T; Yamagishi H
Circ J; 2012; 76(7):1703-11. PubMed ID: 22498567
[TBL] [Abstract][Full Text] [Related]
16. Functionally significant, novel GATA4 variants are frequently associated with Tetralogy of Fallot.
Dixit R; Narasimhan C; Balekundri VI; Agrawal D; Kumar A; Mohapatra B
Hum Mutat; 2018 Dec; 39(12):1957-1972. PubMed ID: 30152191
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Congenital heart diseases and their association with the variant distribution features on susceptibility genes.
Su W; Zhu P; Wang R; Wu Q; Wang M; Zhang X; Mei L; Tang J; Kumar M; Wang X; Su L; Dong N
Clin Genet; 2017 Mar; 91(3):349-354. PubMed ID: 27426723
[TBL] [Abstract][Full Text] [Related]
19. The Functional Polymorphism R129W in the
Shi Y; Li Y; Wang Y; Zhuang J; Wang H; Hu M; Mo X; Yue S; Chen Y; Fan X; Chen J; Cai W; Zhu X; Wan Y; Zhong Y; Ye X; Li F; Zhou Z; Dai G; Luo R; Ocorr K; Jiang Z; Li X; Zhu P; Wu X; Yuan W
Genet Test Mol Biomarkers; 2019 Sep; 23(9):601-609. PubMed ID: 31386585
[No Abstract] [Full Text] [Related]
20. GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of Fallot.
El Bouchikhi I; Belhassan K; Moufid FZ; Houssaini MI; Bouguenouch L; Samri I; Bouhrim M; Ouldim K; Atmani S
Afr Health Sci; 2018 Dec; 18(4):922-930. PubMed ID: 30766556
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
