Qiu XB - Search Results

1

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: qiu xb. 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.

2

Effect of exogenous ghrelin on cell differentiation antigen 40 expression in endothelial cells.

Zhang M, Yuan F, Chen H, Qiu X, Fang W. Zhang M, et al. Acta Biochim Biophys Sin (Shanghai). 2007 Dec;39(12):974-81. doi: 10.1111/j.1745-7270.2007.00365.x. Acta Biochim Biophys Sin (Shanghai). 2007. PMID: 18064390 Free article.

3

Inhibition of proliferation and apoptosis of vascular smooth muscle cells by ghrelin.

Zhan M, Yuan F, Liu H, Chen H, Qiu X, Fang W. Zhan M, et al. Acta Biochim Biophys Sin (Shanghai). 2008 Sep;40(9):769-76. Acta Biochim Biophys Sin (Shanghai). 2008. PMID: 18776988 Free article.

4

Percutaneous repair of inadvertent subclavian artery cannulation: a case report.

Shi HY, Qiu XB, Chen H, Liu ZG, Ye Y, Fang WY. Shi HY, et al. Among authors: qiu xb. Chin Med J (Engl). 2009 May 5;122(9):1117-8. Chin Med J (Engl). 2009. PMID: 19493453 No abstract available.

5

Multiple aortico-cameral tunnels associated with bicuspid aortic valve in aged: a case report.

Qiu XB, Shi HY, Liu L, Chen H, Wu WH, Qiu ZK, Zhang W, Fang WY. Qiu XB, et al. Among authors: qiu zk. Chin Med J (Engl). 2009 Sep 20;122(18):2184-5. Chin Med J (Engl). 2009. PMID: 19781308 No abstract available.

6

Recurrent acute myocardial infarction after 32 months: very late stent thrombosis after sirolimus-eluting stent implantation.

Hou XM, Qiu XB, Fang WY. Hou XM, et al. Among authors: qiu xb. Chin Med J (Engl). 2009 Oct 5;122(19):2399-400. Chin Med J (Engl). 2009. PMID: 20079148 No abstract available.

7

Spontaneous resolution of iatrogenic coronary artery to right ventricular fistula secondary to percutaneous coronary intervention.

Qiu XB, Liu L, Hou XM, Han WZ, Ye Y, Dai JJ, Shi HY, Fang WY. Qiu XB, et al. Chin Med J (Engl). 2013;126(11):2195-6. Chin Med J (Engl). 2013. PMID: 23769583 No abstract available.

8

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.

9

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

10

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.

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