290 related articles for article (PubMed ID: 26118961)
1. TBX20 loss-of-function mutation associated with familial dilated cardiomyopathy.
Zhao CM; Bing-Sun ; Song HM; Wang J; Xu WJ; Jiang JF; Qiu XB; Yuan F; Xu JH; Yang YQ
Clin Chem Lab Med; 2016 Feb; 54(2):325-32. PubMed ID: 26118961
[TBL] [Abstract][Full Text] [Related]
2. TBX5 loss-of-function mutation contributes to familial dilated cardiomyopathy.
Zhang XL; Qiu XB; Yuan F; Wang J; Zhao CM; Li RG; Xu L; Xu YJ; Shi HY; Hou XM; Qu XK; Xu YW; Yang YQ
Biochem Biophys Res Commun; 2015 Mar; 459(1):166-71. PubMed ID: 25725155
[TBL] [Abstract][Full Text] [Related]
3. A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmias.
Yuan F; Qiu XB; Li RG; Qu XK; Wang J; Xu YJ; Liu X; Fang WY; Yang YQ; Liao DN
Int J Mol Med; 2015 Feb; 35(2):478-86. PubMed ID: 25503402
[TBL] [Abstract][Full Text] [Related]
4. Prevalence and spectrum of GATA4 mutations associated with sporadic dilated cardiomyopathy.
Li J; Liu WD; Yang ZL; Yuan F; Xu L; Li RG; Yang YQ
Gene; 2014 Sep; 548(2):174-81. PubMed ID: 25017055
[TBL] [Abstract][Full Text] [Related]
5. A novel TBX20 loss‑of‑function mutation contributes to adult‑onset dilated cardiomyopathy or congenital atrial septal defect.
Zhou YM; Dai XY; Huang RT; Xue S; Xu YJ; Qiu XB; Yang YQ
Mol Med Rep; 2016 Oct; 14(4):3307-14. PubMed ID: 27510170
[TBL] [Abstract][Full Text] [Related]
6. 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]
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. A novel TBX5 loss-of-function mutation associated with sporadic dilated cardiomyopathy.
Zhou W; Zhao L; Jiang JQ; Jiang WF; Yang YQ; Qiu XB
Int J Mol Med; 2015 Jul; 36(1):282-8. PubMed ID: 25963046
[TBL] [Abstract][Full Text] [Related]
9. Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated Cardiomyopathy.
Xu JH; Gu JY; Guo YH; Zhang H; Qiu XB; Li RG; Shi HY; Liu H; Yang XX; Xu YJ; Qu XK; Yang YQ
Int Heart J; 2017 Aug; 58(4):521-529. PubMed ID: 28690296
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. TBX20 loss-of-function mutation contributes to double outlet right ventricle.
Pan Y; Geng R; Zhou N; Zheng GF; Zhao H; Wang J; Zhao CM; Qiu XB; Yang YQ; Liu XY
Int J Mol Med; 2015 Apr; 35(4):1058-66. PubMed ID: 25625280
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. HAND1 loss-of-function mutation associated with familial dilated cardiomyopathy.
Zhou YM; Dai XY; Qiu XB; Yuan F; Li RG; Xu YJ; Qu XK; Huang RT; Xue S; Yang YQ
Clin Chem Lab Med; 2016 Jul; 54(7):1161-7. PubMed ID: 26581070
[TBL] [Abstract][Full Text] [Related]
14. Identification and Functional Characterization of an ISL1 Mutation Predisposing to Dilated Cardiomyopathy.
Xu YJ; Wang ZS; Yang CX; Di RM; Qiao Q; Li XM; Gu JN; Guo XJ; Yang YQ
J Cardiovasc Transl Res; 2019 Jun; 12(3):257-267. PubMed ID: 30536204
[TBL] [Abstract][Full Text] [Related]
15. CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy.
Qiu XB; Qu XK; Li RG; Liu H; Xu YJ; Zhang M; Shi HY; Hou XM; Liu X; Yuan F; Sun YM; Wang J; Huang RT; Xue S; Yang YQ
Clin Chem Lab Med; 2017 Aug; 55(9):1417-1425. PubMed ID: 28099117
[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. Prevalence and spectrum of LRRC10 mutations associated with idiopathic dilated cardiomyopathy.
Qu XK; Yuan F; Li RG; Xu L; Jing WF; Liu H; Xu YJ; Zhang M; Liu X; Fang WY; Yang YQ; Qiu XB
Mol Med Rep; 2015 Sep; 12(3):3718-3724. PubMed ID: 26017719
[TBL] [Abstract][Full Text] [Related]
18. ZBTB17 loss-of-function mutation contributes to familial dilated cardiomyopathy.
Sun YM; Wang J; Xu YJ; Wang XH; Yuan F; Liu H; Li RG; Zhang M; Li YJ; Shi HY; Zhao L; Qiu XB; Qu XK; Yang YQ
Heart Vessels; 2018 Jul; 33(7):722-732. PubMed ID: 29445930
[TBL] [Abstract][Full Text] [Related]
19. MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy.
Yuan F; Qiu ZH; Wang XH; Sun YM; Wang J; Li RG; Liu H; Zhang M; Shi HY; Zhao L; Jiang WF; Liu X; Qiu XB; Qu XK; Yang YQ
Clin Chem Lab Med; 2018 Feb; 56(3):502-511. PubMed ID: 28902616
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]