299 related articles for article (PubMed ID: 31171573)
1. 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]
2. Association of GDF1 rs4808863 with fetal congenital heart defects: a case-control study.
Zhang J; Wu Q; Wang L; Li X; Ma Y; Yao L
BMJ Open; 2015 Dec; 5(12):e009352. PubMed ID: 26656983
[TBL] [Abstract][Full Text] [Related]
3. Homocysteine downregulates cardiac homeobox transcription factor NKX2.5 via IGFBP5.
Lai G; Wang L; Li Z; Zhao Y
Am J Physiol Heart Circ Physiol; 2020 Dec; 319(6):H1380-H1386. PubMed ID: 33035436
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Novel Point Mutations in the
Khatami M; Mazidi M; Taher S; Heidari MM; Hadadzadeh M
Medicina (Kaunas); 2018 Jun; 54(3):. PubMed ID: 30344277
[No Abstract] [Full Text] [Related]
6. 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]
7. Association of growth/differentiation factor 1 gene polymorphisms with the risk of congenital heart disease in the Chinese Han population.
Sun X; Meng Y; You T; Li P; Wu H; Yu M; Xie X
Mol Biol Rep; 2013 Feb; 40(2):1291-9. PubMed ID: 23076529
[TBL] [Abstract][Full Text] [Related]
8. Functional analysis of novel genetic variants of NKX2-5 associated with nonsyndromic congenital heart disease.
Dixit R; Narasimhan C; Balekundri VI; Agrawal D; Kumar A; Mohapatra B
Am J Med Genet A; 2021 Dec; 185(12):3644-3663. PubMed ID: 34214246
[TBL] [Abstract][Full Text] [Related]
9. A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis.
Sun YM; Wang J; Qiu XB; Yuan F; Li RG; Xu YJ; Qu XK; Shi HY; Hou XM; Huang RT; Xue S; Yang YQ
G3 (Bethesda); 2016 Apr; 6(4):987-92. PubMed ID: 26865696
[TBL] [Abstract][Full Text] [Related]
10. Two novel and functional DNA sequence variants within an upstream enhancer of the human NKX2-5 gene in ventricular septal defects.
Huang W; Meng H; Qiao Y; Pang S; Chen D; Yan B
Gene; 2013 Jul; 524(2):152-5. PubMed ID: 23644027
[TBL] [Abstract][Full Text] [Related]
11. R25C mutation in the NKX2.5 gene in Italian patients affected with non-syndromic and syndromic congenital heart disease.
Beffagna G; Cecchetto A; Dal Bianco L; Lorenzon A; Angelini A; Padalino M; Vida V; Bhattacharya S; Stellin G; Rampazzo A; Daliento L
J Cardiovasc Med (Hagerstown); 2013 Aug; 14(8):582-6. PubMed ID: 22964646
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. [NKX2.5 and TBX5 gene mutations in in vitro fertilization children with congenital heart disease].
Yang JH; Xu XY; Mi HY; Jiang Y; Ma XM; Li L
Zhongguo Dang Dai Er Ke Za Zhi; 2017 Jun; 19(6):652-657. PubMed ID: 28606231
[TBL] [Abstract][Full Text] [Related]
14. Genetic analysis of an enhancer of the NKX2-5 gene in ventricular septal defects.
Qin X; Xing Q; Ma L; Meng H; Liu Y; Pang S; Yan B
Gene; 2012 Oct; 508(1):106-9. PubMed ID: 22824467
[TBL] [Abstract][Full Text] [Related]
15. Genetic and functional analysis of the NKX2-5 gene promoter in patients with ventricular septal defects.
Pang S; Shan J; Qiao Y; Ma L; Qin X; Wanyan H; Xing Q; Wu G; Yan B
Pediatr Cardiol; 2012 Dec; 33(8):1355-61. PubMed ID: 22576768
[TBL] [Abstract][Full Text] [Related]
16. Search of Somatic Mutations of NKX2-5 and GATA4 Genes in Chinese Patients with Sporadic Congenital Heart Disease.
Yin J; Qian J; Dai G; Wang C; Qin Y; Xu T; Li Z; Zhang H; Yang S
Pediatr Cardiol; 2019 Jan; 40(1):17-22. PubMed ID: 30121862
[TBL] [Abstract][Full Text] [Related]
17. Mutations of NKX2.5 and GATA4 genes in the development of congenital heart disease.
Tong YF
Gene; 2016 Aug; 588(1):86-94. PubMed ID: 27154817
[TBL] [Abstract][Full Text] [Related]
18. Association between congenital heart disease and
González-Castro TB; Tovilla-Zárate CA; López-Narvaez ML; Juárez-Rojop IE; Calderón-Colmenero J; Sandoval JP; García-Montes JA; Blachman-Braun R; Castillo-Avila RG; García-Flores E; Cazarín-Santos BG; Borgonio-Cuadra VM; Posadas-Sánchez R; Vargas-Alarcón G; Rodríguez-Pérez JM; Pérez-Hernández N
Biomark Med; 2020 Dec; 14(18):1747-1757. PubMed ID: 33346701
[No Abstract] [Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
