These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
129 related articles for article (PubMed ID: 22824924)
1. 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]
2. 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]
3. 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]
4. 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]
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 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]
7. 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]
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. 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]
10. 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]
12. GATA6 loss-of-function mutation contributes to congenital bicuspid aortic valve. Xu YJ; Di RM; Qiao Q; Li XM; Huang RT; Xue S; Liu XY; Wang J; Yang YQ Gene; 2018 Jul; 663():115-120. PubMed ID: 29653232 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. GATA6 loss-of-function mutations contribute to familial dilated cardiomyopathy. Xu L; Zhao L; Yuan F; Jiang WF; Liu H; Li RG; Xu YJ; Zhang M; Fang WY; Qu XK; Yang YQ; Qiu XB Int J Mol Med; 2014 Nov; 34(5):1315-22. PubMed ID: 25119427 [TBL] [Abstract][Full Text] [Related]
17. Gain-of-function mutations in GATA6 lead to atrial fibrillation. Tucker NR; Mahida S; Ye J; Abraham EJ; Mina JA; Parsons VA; McLellan MA; Shea MA; Hanley A; Benjamin EJ; Milan DJ; Lin H; Ellinor PT Heart Rhythm; 2017 Feb; 14(2):284-291. PubMed ID: 27756709 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Prevalence and spectrum of GJA5 mutations associated with lone atrial fibrillation. Shi HF; Yang JF; Wang Q; Li RG; Xu YJ; Qu XK; Fang WY; Liu X; Yang YQ Mol Med Rep; 2013 Mar; 7(3):767-74. PubMed ID: 23292621 [TBL] [Abstract][Full Text] [Related]
20. Novel connexin40 missense mutations in patients with familial atrial fibrillation. Yang YQ; Liu X; Zhang XL; Wang XH; Tan HW; Shi HF; Jiang WF; Fang WY Europace; 2010 Oct; 12(10):1421-7. PubMed ID: 20650941 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]