269 related articles for article (PubMed ID: 21637914)
1. A novel GATA4 mutation responsible for congenital ventricular septal defects.
Wang J; Fang M; Liu XY; Xin YF; Liu ZM; Chen XZ; Wang XZ; Fang WY; Liu X; Yang YQ
Int J Mol Med; 2011 Oct; 28(4):557-64. PubMed ID: 21637914
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Involvement of a novel GATA4 mutation in atrial septal defects.
Liu XY; Wang J; Zheng JH; Bai K; Liu ZM; Wang XZ; Liu X; Fang WY; Yang YQ
Int J Mol Med; 2011 Jul; 28(1):17-23. PubMed ID: 21373748
[TBL] [Abstract][Full Text] [Related]
4. A novel GATA4 loss-of-function mutation associated with congenital ventricular septal defect.
Yang YQ; Li L; Wang J; Liu XY; Chen XZ; Zhang W; Wang XZ; Jiang JQ; Liu X; Fang WY
Pediatr Cardiol; 2012 Apr; 33(4):539-46. PubMed ID: 22101736
[TBL] [Abstract][Full Text] [Related]
5. Novel GATA4 mutations in patients with congenital ventricular septal defects.
Yang YQ; Wang J; Liu XY; Chen XZ; Zhang W; Wang XZ; Liu X; Fang WY
Med Sci Monit; 2012 Jun; 18(6):CR344-50. PubMed ID: 22648249
[TBL] [Abstract][Full Text] [Related]
6. GATA4 loss-of-function mutations in familial atrial fibrillation.
Yang YQ; Wang MY; Zhang XL; Tan HW; Shi HF; Jiang WF; Wang XH; Fang WY; Liu X
Clin Chim Acta; 2011 Sep; 412(19-20):1825-30. PubMed ID: 21708142
[TBL] [Abstract][Full Text] [Related]
7. A novel GATA4 loss-of-function mutation responsible for familial dilated cardiomyopathy.
Zhao L; Xu JH; Xu WJ; Yu H; Wang Q; Zheng HZ; Jiang WF; Jiang JF; Yang YQ
Int J Mol Med; 2014 Mar; 33(3):654-60. PubMed ID: 24366163
[TBL] [Abstract][Full Text] [Related]
8. Genetic analysis of the promoter region of the GATA4 gene in patients with ventricular septal defects.
Wu G; Shan J; Pang S; Wei X; Zhang H; Yan B
Transl Res; 2012 May; 159(5):376-82. PubMed ID: 22500510
[TBL] [Abstract][Full Text] [Related]
9. A novel NKX2-5 mutation in familial ventricular septal defect.
Wang J; Xin YF; Liu XY; Liu ZM; Wang XZ; Yang YQ
Int J Mol Med; 2011 Mar; 27(3):369-75. PubMed ID: 21165553
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. [A novel GATA4 mutation leading to congenital ventricular septal defect].
Yang YQ; Tang YQ; Liu XY; Lin XP; Chen YH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Oct; 27(5):512-6. PubMed ID: 20931527
[TBL] [Abstract][Full Text] [Related]
12. GATA4 loss-of-function mutation underlies familial dilated cardiomyopathy.
Li RG; Li L; Qiu XB; Yuan F; Xu L; Li X; Xu YJ; Jiang WF; Jiang JQ; Liu X; Fang WY; Zhang M; Peng LY; Qu XK; Yang YQ
Biochem Biophys Res Commun; 2013 Oct; 439(4):591-6. PubMed ID: 24041700
[TBL] [Abstract][Full Text] [Related]
13. MEF2C loss-of-function mutation contributes to congenital heart defects.
Qiao XH; Wang F; Zhang XL; Huang RT; Xue S; Wang J; Qiu XB; Liu XY; Yang YQ
Int J Med Sci; 2017; 14(11):1143-1153. PubMed ID: 29104469
[TBL] [Abstract][Full Text] [Related]
14. GATA5 loss-of-function mutation responsible for the congenital ventriculoseptal defect.
Wei D; Bao H; Zhou N; Zheng GF; Liu XY; Yang YQ
Pediatr Cardiol; 2013 Mar; 34(3):504-11. PubMed ID: 22961344
[TBL] [Abstract][Full Text] [Related]
15. CASZ1 loss-of-function mutation associated with congenital heart disease.
Huang RT; Xue S; Wang J; Gu JY; Xu JH; Li YJ; Li N; Yang XX; Liu H; Zhang XD; Qu XK; Xu YJ; Qiu XB; Li RG; Yang YQ
Gene; 2016 Dec; 595(1):62-68. PubMed ID: 27693370
[TBL] [Abstract][Full Text] [Related]
16. A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect.
Qiao XH; Wang Q; Wang J; Liu XY; Xu YJ; Huang RT; Xue S; Li YJ; Zhang M; Qu XK; Li RG; Qiu XB; Yang YQ
Eur J Med Genet; 2018 Apr; 61(4):197-203. PubMed ID: 29222010
[TBL] [Abstract][Full Text] [Related]
17. [Novel GATA4 mutations identified in patients with congenital atrial septal defects].
Liu XY; Yang YQ; Ma J; Lin XP; Zheng JH; Bai K; Chen YH
Zhonghua Xin Xue Guan Bing Za Zhi; 2010 Aug; 38(8):724-7. PubMed ID: 21055141
[TBL] [Abstract][Full Text] [Related]
18. A Novel TBX1 Loss-of-Function Mutation Associated with Congenital Heart Disease.
Pan Y; Wang ZG; Liu XY; Zhao H; Zhou N; Zheng GF; Qiu XB; Li RG; Yuan F; Shi HY; Hou XM; Yang YQ
Pediatr Cardiol; 2015 Oct; 36(7):1400-10. PubMed ID: 25860641
[TBL] [Abstract][Full Text] [Related]
19. GATA6 loss-of-function mutation in atrial fibrillation.
Yang YQ; Li L; Wang J; Zhang XL; Li RG; Xu YJ; Tan HW; Wang XH; Jiang JQ; Fang WY; Liu X
Eur J Med Genet; 2012 Oct; 55(10):520-6. PubMed ID: 22750565
[TBL] [Abstract][Full Text] [Related]
20. A novel NKX2.6 mutation associated with congenital ventricular septal defect.
Wang J; Mao JH; Ding KK; Xu WJ; Liu XY; Qiu XB; Li RG; Qu XK; Xu YJ; Huang RT; Xue S; Yang YQ
Pediatr Cardiol; 2015 Mar; 36(3):646-56. PubMed ID: 25380965
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]