Zhang M - Search Results

1

GATA4 Loss-of-Function Mutation and the Congenitally Bicuspid Aortic Valve.

Li RG, Xu YJ, Wang J, Liu XY, Yuan F, Huang RT, Xue S, Li L, Liu H, Li YJ, Qu XK, Shi HY, Zhang M, Qiu XB, Yang YQ. Li RG, et al. Among authors: zhang m. Am J Cardiol. 2018 Feb 15;121(4):469-474. doi: 10.1016/j.amjcard.2017.11.012. Epub 2017 Nov 23. Am J Cardiol. 2018. PMID: 29325903

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: 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.

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: 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

4

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

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

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. Among authors: zhang m. Clin Chem Lab Med. 2018 Feb 23;56(3):502-511. doi: 10.1515/cclm-2017-0461. Clin Chem Lab Med. 2018. PMID: 28902616

7

A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect.

Qiao XH, Wang Q, Wang J, Liu XY, Xu YJ, Huang RT, Xue S, Li YJ, Zhang M, Qu XK, Li RG, Qiu XB, Yang YQ. Qiao XH, et al. Among authors: zhang m. Eur J Med Genet. 2018 Apr;61(4):197-203. doi: 10.1016/j.ejmg.2017.12.003. Epub 2017 Dec 6. Eur J Med Genet. 2018. PMID: 29222010

8

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. Sun YM, et al. Among authors: zhang m. Heart Vessels. 2018 Jul;33(7):722-732. doi: 10.1007/s00380-017-1110-4. Epub 2018 Feb 14. Heart Vessels. 2018. PMID: 29445930

9

HAND2 loss-of-function mutation causes familial dilated cardiomyopathy.

Liu H, Xu YJ, Li RG, Wang ZS, Zhang M, Qu XK, Qiao Q, Li XM, Di RM, Qiu XB, Yang YQ. Liu H, et al. Among authors: zhang m. Eur J Med Genet. 2019 Sep;62(9):103540. doi: 10.1016/j.ejmg.2018.09.007. Epub 2018 Sep 12. Eur J Med Genet. 2019. PMID: 30217752

10

ISL1 loss-of-function mutation contributes to congenital heart defects.

Ma L, Wang J, Li L, Qiao Q, Di RM, Li XM, Xu YJ, Zhang M, Li RG, Qiu XB, Li X, Yang YQ. Ma L, et al. Among authors: zhang m. Heart Vessels. 2019 Apr;34(4):658-668. doi: 10.1007/s00380-018-1289-z. Epub 2018 Nov 2. Heart Vessels. 2019. PMID: 30390123

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