Zhang M - Search Results

1

Detection and functional characterization of a novel MEF2A variation responsible for familial dilated cardiomyopathy.

Qiao Q, Zhao CM, Yang CX, Gu JN, Guo YH, Zhang M, Li RG, Qiu XB, Xu YJ, Yang YQ. Qiao Q, et al. Among authors: zhang m. Clin Chem Lab Med. 2020 Dec 3;59(5):955-963. doi: 10.1515/cclm-2020-1318. Print 2021 Apr 27. Clin Chem Lab Med. 2020. PMID: 33554560

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

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

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: zhang m. Clin Chem Lab Med. 2017 Aug 28;55(9):1417-1425. doi: 10.1515/cclm-2016-0612. Clin Chem Lab Med. 2017. PMID: 28099117

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

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

8

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

9

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

10

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

57,267 results

Search Page