Zhang M - Search Results

1

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. Li RG, et al. Among authors: zhang m. Int J Mol Med. 2013 Jul;32(1):144-50. doi: 10.3892/ijmm.2013.1355. Epub 2013 Apr 22. Int J Mol Med. 2013. PMID: 23604097

2

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: zhang m. 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

3

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: zhang m. 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

4

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: zhang m. 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

5

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: zhang m. 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.

6

A SHOX2 loss-of-function mutation underlying familial atrial fibrillation.

Li N, Wang ZS, Wang XH, Xu YJ, Qiao Q, Li XM, Di RM, Guo XJ, Li RG, Zhang M, Qiu XB, Yang YQ. Li N, et al. Among authors: zhang m. Int J Med Sci. 2018 Oct 20;15(13):1564-1572. doi: 10.7150/ijms.27424. eCollection 2018. Int J Med Sci. 2018. PMID: 30443179 Free PMC article.

7

NR2F2 loss‑of‑function mutation is responsible for congenital bicuspid aortic valve.

Wang J, Abhinav P, Xu YJ, Li RG, Zhang M, Qiu XB, Di RM, Qiao Q, Li XM, Huang RT, Xue S, Yang YQ. Wang J, et al. Among authors: zhang m. Int J Mol Med. 2019 Apr;43(4):1839-1846. doi: 10.3892/ijmm.2019.4087. Epub 2019 Jan 31. Int J Mol Med. 2019. PMID: 30720060

8

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: zhang m. 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.

9

Utility of 64-MSCT in assessing acute non-reperfused myocardial infarct size.

Qu XK, Fang WY, Ye JD, Guan SF, Li RG, Xu YJ, Shen Y, Zhang M, Liu H. Qu XK, et al. Among authors: zhang m. J Geriatr Cardiol. 2013 Sep;10(3):247-52. doi: 10.3969/j.issn.1671-5411.2013.03.007. J Geriatr Cardiol. 2013. PMID: 24133512 Free PMC article.

10

MESP1 loss‑of‑function mutation contributes to double outlet right ventricle.

Zhang M, Li FX, Liu XY, Huang RT, Xue S, Yang XX, Li YJ, Liu H, Shi HY, Pan X, Qiu XB, Yang YQ. Zhang M, et al. Mol Med Rep. 2017 Sep;16(3):2747-2754. doi: 10.3892/mmr.2017.6875. Epub 2017 Jun 29. Mol Med Rep. 2017. PMID: 28677747

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