Yuan F - Search Results

1

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. Li RG, et al. Among authors: yuan f. Biochem Biophys Res Commun. 2013 Oct 4;439(4):591-6. doi: 10.1016/j.bbrc.2013.09.023. Epub 2013 Sep 13. Biochem Biophys Res Commun. 2013. PMID: 24041700 Free article.

2

[Dual chamber pacing for vasovagal syncope].

Liu ZG, Gao DS, Yuan F, Ye Y, Cui KJ, Liu X. Liu ZG, et al. Among authors: yuan f. Zhonghua Xin Xue Guan Bing Za Zhi. 2005 Jan;33(1):30-3. Zhonghua Xin Xue Guan Bing Za Zhi. 2005. PMID: 15924774 Chinese.

3

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. Shi LM, et al. Among authors: yuan f. Int J Mol Med. 2014 May;33(5):1219-26. doi: 10.3892/ijmm.2014.1700. Epub 2014 Mar 14. Int J Mol Med. 2014. PMID: 24638895

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. Li J, et al. Among authors: yuan f. Gene. 2014 Sep 15;548(2):174-81. doi: 10.1016/j.gene.2014.07.022. Epub 2014 Jul 10. Gene. 2014. PMID: 25017055

5

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. Xu L, et al. Among authors: yuan f. Int J Mol Med. 2014 Nov;34(5):1315-22. doi: 10.3892/ijmm.2014.1896. Epub 2014 Aug 13. Int J Mol Med. 2014. PMID: 25119427

6

Prevalence and spectrum of Nkx2.6 mutations in patients with congenital heart disease.

Zhao L, Ni SH, Liu XY, Wei D, Yuan F, Xu L, Xin-Li, Li RG, Qu XK, Xu YJ, Fang WY, Yang YQ, Qiu XB. Zhao L, et al. Among authors: yuan f. Eur J Med Genet. 2014 Oct;57(10):579-86. doi: 10.1016/j.ejmg.2014.08.005. Epub 2014 Sep 3. Eur J Med Genet. 2014. PMID: 25195019

7

A novel NKX2.5 loss-of-function mutation associated with congenital bicuspid aortic valve.

Qu XK, Qiu XB, Yuan F, Wang J, Zhao CM, Liu XY, Zhang XL, Li RG, Xu YJ, Hou XM, Fang WY, Liu X, Yang YQ. Qu XK, et al. Among authors: yuan f. Am J Cardiol. 2014 Dec 15;114(12):1891-5. doi: 10.1016/j.amjcard.2014.09.028. Epub 2014 Sep 28. Am J Cardiol. 2014. PMID: 25438918

8

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. Yuan F, et al. Int J Mol Med. 2015 Feb;35(2):478-86. doi: 10.3892/ijmm.2014.2029. Epub 2014 Dec 9. Int J Mol Med. 2015. PMID: 25503402 Clinical Trial.

9

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. Zhang XL, et al. Among authors: yuan f. Int J Mol Med. 2015 Mar;35(3):763-70. doi: 10.3892/ijmm.2014.2050. Epub 2014 Dec 29. Int J Mol Med. 2015. PMID: 25543888

10

Ghrelin receptor deficiency aggravates atherosclerotic plaque instability.

Zhang M, Qu X, Yuan F, Yang Y, Xu L, Dai J, Wang W, Fei J, Hou X, Fang W. Zhang M, et al. Among authors: yuan f. Front Biosci (Landmark Ed). 2015 Jan 1;20(4):604-13. doi: 10.2741/4325. Front Biosci (Landmark Ed). 2015. PMID: 25553467 Free article.

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