134 related articles for article (PubMed ID: 20818502)
1. Connexin40 nonsense mutation in familial atrial fibrillation.
Yang YQ; Zhang XL; Wang XH; Tan HW; Shi HF; Jiang WF; Fang WY; Liu X
Int J Mol Med; 2010 Oct; 26(4):605-10. PubMed ID: 20818502
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. Novel germline GJA5/connexin40 mutations associated with lone atrial fibrillation impair gap junctional intercellular communication.
Sun Y; Yang YQ; Gong XQ; Wang XH; Li RG; Tan HW; Liu X; Fang WY; Bai D
Hum Mutat; 2013 Apr; 34(4):603-9. PubMed ID: 23348765
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. An atrial-fibrillation-linked connexin40 mutant is retained in the endoplasmic reticulum and impairs the function of atrial gap-junction channels.
Sun Y; Tong X; Chen H; Huang T; Shao Q; Huang W; Laird DW; Bai D
Dis Model Mech; 2014 May; 7(5):561-9. PubMed ID: 24626989
[TBL] [Abstract][Full Text] [Related]
10. Mutations of the SCN4B-encoded sodium channel β4 subunit in familial atrial fibrillation.
Li RG; Wang Q; Xu YJ; Zhang M; Qu XK; Liu X; Fang WY; Yang YQ
Int J Mol Med; 2013 Jul; 32(1):144-50. PubMed ID: 23604097
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. ISL1 loss-of-function variation causes familial atrial fibrillation.
Wu SH; Wang XH; Xu YJ; Gu JN; Yang CX; Qiao Q; Guo XJ; Guo YH; Qiu XB; Jiang WF; Yang YQ
Eur J Med Genet; 2020 Nov; 63(11):104029. PubMed ID: 32771629
[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. Connexin45 (GJC1) loss-of-function mutation contributes to familial atrial fibrillation and conduction disease.
Li RG; Xu YJ; Ye WG; Li YJ; Chen H; Qiu XB; Yang YQ; Bai D
Heart Rhythm; 2021 May; 18(5):684-693. PubMed ID: 33429106
[TBL] [Abstract][Full Text] [Related]
15. The Connexin40A96S mutation from a patient with atrial fibrillation causes decreased atrial conduction velocities and sustained episodes of induced atrial fibrillation in mice.
Lübkemeier I; Andrié R; Lickfett L; Bosen F; Stöckigt F; Dobrowolski R; Draffehn AM; Fregeac J; Schultze JL; Bukauskas FF; Schrickel JW; Willecke K
J Mol Cell Cardiol; 2013 Dec; 65():19-32. PubMed ID: 24060583
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. 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]
20. Atrial fibrillation-linked GJA5/connexin40 mutants impaired gap junctions via different mechanisms.
Bai D
FEBS Lett; 2014 Apr; 588(8):1238-43. PubMed ID: 24656738
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]