Yuan F - Search Results

1

[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.

2

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.

3

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

4

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.

5

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. Qu XK, et al. Among authors: yuan f. Mol Med Rep. 2015 Sep;12(3):3718-3724. doi: 10.3892/mmr.2015.3843. Epub 2015 May 25. Mol Med Rep. 2015. PMID: 26017719

6

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. Wang ZC, et al. Among authors: yuan f. Int J Med Sci. 2016 Jan 23;13(1):60-7. doi: 10.7150/ijms.13264. eCollection 2016. Int J Med Sci. 2016. PMID: 26917986 Free PMC article.

7

TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome.

Guo DF, Li RG, Yuan F, Shi HY, Hou XM, Qu XK, Xu YJ, Zhang M, Liu X, Jiang JQ, Yang YQ, Qiu XB. Guo DF, et al. Among authors: yuan f. Mol Med Rep. 2016 May;13(5):4349-56. doi: 10.3892/mmr.2016.5043. Epub 2016 Mar 24. Mol Med Rep. 2016. PMID: 27035640 Clinical Trial.

8

Prevalence and spectrum of NKX2.5 mutations in patients with congenital atrial septal defect and atrioventricular block.

Xu YJ, Qiu XB, Yuan F, Shi HY, Xu L, Hou XM, Qu XK, Liu X, Huang RT, Xue S, Yang YQ, Li RG. Xu YJ, et al. Among authors: yuan f. Mol Med Rep. 2017 Apr;15(4):2247-2254. doi: 10.3892/mmr.2017.6249. Epub 2017 Feb 24. Mol Med Rep. 2017. PMID: 28259982

9

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. Yuan F, et al. Clin Chem Lab Med. 2018 Feb 23;56(3):502-511. doi: 10.1515/cclm-2017-0461. Clin Chem Lab Med. 2018. PMID: 28902616

10

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. Qiu XB, et al. Among authors: yuan f. Clin Chem Lab Med. 2017 Aug 28;55(9):1417-1425. doi: 10.1515/cclm-2016-0612. Clin Chem Lab Med. 2017. PMID: 28099117

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