130 related articles for article (PubMed ID: 23175127)
1. A novel GATA5 loss-of-function mutation underlies lone atrial fibrillation.
Wang XH; Huang CX; Wang Q; Li RG; Xu YJ; Liu X; Fang WY; Yang YQ
Int J Mol Med; 2013 Jan; 31(1):43-50. PubMed ID: 23175127
[TBL] [Abstract][Full Text] [Related]
2. Novel GATA5 loss-of-function mutations underlie familial atrial fibrillation.
Gu JY; Xu JH; Yu H; Yang YQ
Clinics (Sao Paulo); 2012 Dec; 67(12):1393-9. PubMed ID: 23295592
[TBL] [Abstract][Full Text] [Related]
3. Novel GATA6 loss-of-function mutation responsible for familial atrial fibrillation.
Li J; Liu WD; Yang ZL; Yang YQ
Int J Mol Med; 2012 Oct; 30(4):783-90. PubMed ID: 22824924
[TBL] [Abstract][Full Text] [Related]
4. GATA5 loss-of-function mutation in familial dilated cardiomyopathy.
Zhang XL; Dai N; Tang K; Chen YQ; Chen W; Wang J; Zhao CM; Yuan F; Qiu XB; Qu XK; Yang YQ; Xu YW
Int J Mol Med; 2015 Mar; 35(3):763-70. PubMed ID: 25543888
[TBL] [Abstract][Full Text] [Related]
5. Novel GATA4 mutations in lone atrial fibrillation.
Jiang JQ; Shen FF; Fang WY; Liu X; Yang YQ
Int J Mol Med; 2011 Dec; 28(6):1025-32. PubMed ID: 21874226
[TBL] [Abstract][Full Text] [Related]
6. A novel PITX2c loss‑of‑function mutation underlies lone atrial fibrillation.
Zhou YM; Zheng PX; Yang YQ; Ge ZM; Kang WQ
Int J Mol Med; 2013 Oct; 32(4):827-34. PubMed ID: 23913021
[TBL] [Abstract][Full Text] [Related]
7. A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation.
Huang RT; Xue S; Xu YJ; Zhou M; Yang YQ
Int J Mol Med; 2013 May; 31(5):1119-26. PubMed ID: 23525379
[TBL] [Abstract][Full Text] [Related]
8. NKX2-6 mutation predisposes to familial atrial fibrillation.
Wang J; Zhang DF; Sun YM; Li RG; Qiu XB; Qu XK; Liu X; Fang WY; Yang YQ
Int J Mol Med; 2014 Dec; 34(6):1581-90. PubMed ID: 25319568
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. GATA5 loss-of-function mutations underlie tetralogy of fallot.
Wei D; Bao H; Liu XY; Zhou N; Wang Q; Li RG; Xu YJ; Yang YQ
Int J Med Sci; 2013; 10(1):34-42. PubMed ID: 23289003
[TBL] [Abstract][Full Text] [Related]
11. Mutational spectrum of the NKX2-5 gene in patients with lone atrial fibrillation.
Yu H; Xu JH; Song HM; Zhao L; Xu WJ; Wang J; Li RG; Xu L; Jiang WF; Qiu XB; Jiang JQ; Qu XK; Liu X; Fang WY; Jiang JF; Yang YQ
Int J Med Sci; 2014; 11(6):554-63. PubMed ID: 24782644
[TBL] [Abstract][Full Text] [Related]
12. Mutation spectrum of the GATA4 gene in patients with idiopathic atrial fibrillation.
Wang J; Sun YM; Yang YQ
Mol Biol Rep; 2012 Aug; 39(8):8127-35. PubMed ID: 22552926
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation.
Xie WH; Chang C; Xu YJ; Li RG; Qu XK; Fang WY; Liu X; Yang YQ
Clinics (Sao Paulo); 2013 Jun; 68(6):777-84. PubMed ID: 23778487
[TBL] [Abstract][Full Text] [Related]
15. A novel PITX2c loss-of-function mutation associated with familial atrial fibrillation.
Wang J; Zhang DF; Sun YM; Yang YQ
Eur J Med Genet; 2014 Jan; 57(1):25-31. PubMed ID: 24333117
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Prevalence and Spectrum of TBX5 Mutation in Patients with Lone Atrial Fibrillation.
Wang ZC; Ji WH; Ruan CW; Liu XY; Qiu XB; Yuan F; Li RG; Xu YJ; Liu X; Huang RT; Xue S; Yang YQ
Int J Med Sci; 2016; 13(1):60-7. PubMed ID: 26917986
[TBL] [Abstract][Full Text] [Related]
18. GATA5 loss-of-function mutations associated with congenital bicuspid aortic valve.
Shi LM; Tao JW; Qiu XB; Wang J; Yuan F; Xu L; Liu H; Li RG; Xu YJ; Wang Q; Zheng HZ; Li X; Wang XZ; Zhang M; Qu XK; Yang YQ
Int J Mol Med; 2014 May; 33(5):1219-26. PubMed ID: 24638895
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. A
Li N; Wang ZS; Wang XH; Xu YJ; Qiao Q; Li XM; Di RM; Guo XJ; Li RG; Zhang M; Qiu XB; Yang YQ
Int J Med Sci; 2018; 15(13):1564-1572. PubMed ID: 30443179
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]