Qiu XB - Search Results

1

HAND1 loss-of-function mutation associated with familial dilated cardiomyopathy.

Zhou YM, Dai XY, Qiu XB, Yuan F, Li RG, Xu YJ, Qu XK, Huang RT, Xue S, Yang YQ. Zhou YM, et al. Among authors: qiu xb. Clin Chem Lab Med. 2016 Jul 1;54(7):1161-7. doi: 10.1515/cclm-2015-0766. Clin Chem Lab Med. 2016. PMID: 26581070

2

PITX2c loss-of-function mutations responsible for congenital atrial septal defects.

Yuan F, Zhao L, Wang J, Zhang W, Li X, Qiu XB, Li RG, Xu YJ, Xu L, Qu XK, Fang WY, Yang YQ. Yuan F, et al. Among authors: qiu xb. Int J Med Sci. 2013 Aug 22;10(10):1422-9. doi: 10.7150/ijms.6809. eCollection 2013. Int J Med Sci. 2013. PMID: 23983605 Free PMC article.

3

GATA4 loss-of-function mutations underlie familial tetralogy of fallot.

Yang YQ, Gharibeh L, Li RG, Xin YF, Wang J, Liu ZM, Qiu XB, Xu YJ, Xu L, Qu XK, Liu X, Fang WY, Huang RT, Xue S, Nemer G. Yang YQ, et al. Among authors: qiu xb. Hum Mutat. 2013 Dec;34(12):1662-71. doi: 10.1002/humu.22434. Epub 2013 Sep 17. Hum Mutat. 2013. PMID: 24000169

4

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: qiu xb. 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.

5

Prevalence and spectrum of PITX2c mutations associated with congenital heart disease.

Wang J, Xin YF, Xu WJ, Liu ZM, Qiu XB, Qu XK, Xu L, Li X, Yang YQ. Wang J, et al. Among authors: qiu xb. DNA Cell Biol. 2013 Dec;32(12):708-16. doi: 10.1089/dna.2013.2185. Epub 2013 Oct 1. DNA Cell Biol. 2013. PMID: 24083357 Free PMC article.

6

PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillation.

Qiu XB, Xu YJ, Li RG, Xu L, Liu X, Fang WY, Yang YQ, Qu XK. Qiu XB, et al. Clinics (Sao Paulo). 2014 Jan;69(1):15-22. doi: 10.6061/clinics/2014(01)03. Clinics (Sao Paulo). 2014. PMID: 24473555 Free PMC article.

7

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: qiu xb. 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

8

Mutational spectrum of the NKX2-5 gene in patients with lone atrial fibrillation.

Yu H, Xu JH, Song HM, Zhao L, Xu WJ, Wang J, Li RG, Xu L, Jiang WF, Qiu XB, Jiang JQ, Qu XK, Liu X, Fang WY, Jiang JF, Yang YQ. Yu H, et al. Among authors: qiu xb. Int J Med Sci. 2014 Apr 7;11(6):554-63. doi: 10.7150/ijms.8407. eCollection 2014. Int J Med Sci. 2014. PMID: 24782644 Free PMC article.

9

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: qiu xb. 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

10

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: qiu xb. 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

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