Xue S - Search Results

1

TBX1 loss-of-function mutation contributes to congenital conotruncal defects.

Zhang M, Li FX, Liu XY, Hou JY, Ni SH, Wang J, Zhao CM, Zhang W, Kong Y, Huang RT, Xue S, Yang YQ. Zhang M, et al. Among authors: xue s. Exp Ther Med. 2018 Jan;15(1):447-453. doi: 10.3892/etm.2017.5362. Epub 2017 Oct 24. Exp Ther Med. 2018. PMID: 29250159 Free PMC article.

2

[Effects of acupuncture-drug compound anesthesia on perioperative inflammatory factors in patients undergoing cardiac surgery].

Shan JG, Xue S, Xu GX, Wang WJ, Lian F, Liu S, Hu ZL, Huang RT. Shan JG, et al. Among authors: xue s. Zhongguo Zhen Jiu. 2010 Jul;30(7):585-8. Zhongguo Zhen Jiu. 2010. PMID: 20862944 Clinical Trial. Chinese.

3

Meta-analysis of clinical studies comparing coronary artery bypass grafting with percutaneous coronary intervention in patients with end-stage renal disease.

Zheng H, Xue S, Lian F, Huang RT, Hu ZL, Wang YY. Zheng H, et al. Among authors: xue s. Eur J Cardiothorac Surg. 2013 Mar;43(3):459-67. doi: 10.1093/ejcts/ezs360. Epub 2012 Jul 9. Eur J Cardiothorac Surg. 2013. PMID: 22778175 Review.

4

Somatic mutations in the GATA6 gene underlie sporadic tetralogy of Fallot.

Huang RT, Xue S, Xu YJ, Yang YQ. Huang RT, et al. Among authors: xue s. Int J Mol Med. 2013 Jan;31(1):51-8. doi: 10.3892/ijmm.2012.1188. Epub 2012 Nov 20. Int J Mol Med. 2013. PMID: 23175051

5

A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation.

Huang RT, Xue S, Xu YJ, Zhou M, Yang YQ. Huang RT, et al. Among authors: xue s. Int J Mol Med. 2013 May;31(5):1119-26. doi: 10.3892/ijmm.2013.1316. Epub 2013 Mar 22. Int J Mol Med. 2013. PMID: 23525379

6

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: xue s. Hum Mutat. 2013 Dec;34(12):1662-71. doi: 10.1002/humu.22434. Epub 2013 Sep 17. Hum Mutat. 2013. PMID: 24000169

7

Somatic GATA5 mutations in sporadic tetralogy of Fallot.

Huang RT, Xue S, Xu YJ, Zhou M, Yang YQ. Huang RT, et al. Among authors: xue s. Int J Mol Med. 2014 May;33(5):1227-35. doi: 10.3892/ijmm.2014.1674. Epub 2014 Feb 26. Int J Mol Med. 2014. PMID: 24573614

8

A novel NKX2.6 mutation associated with congenital ventricular septal defect.

Wang J, Mao JH, Ding KK, Xu WJ, Liu XY, Qiu XB, Li RG, Qu XK, Xu YJ, Huang RT, Xue S, Yang YQ. Wang J, et al. Among authors: xue s. Pediatr Cardiol. 2015 Mar;36(3):646-56. doi: 10.1007/s00246-014-1060-x. Epub 2014 Nov 8. Pediatr Cardiol. 2015. PMID: 25380965

9

Identification and characterization of CD4(+)AT2(+) T lymphocyte population in human thoracic aortic aneurysm.

Wang C, Wu T, Hu X, Huang R, Lian F, Wang W, Feng Y, Xie B, Hu Z, Zhai X, Liu J, Gu J, Chen Y, Li J, Xue S. Wang C, et al. Among authors: xue s. Am J Transl Res. 2015 Feb 15;7(2):232-41. eCollection 2015. Am J Transl Res. 2015. PMID: 25901193 Free PMC article.

10

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: xue s. Clin Chem Lab Med. 2016 Jul 1;54(7):1161-7. doi: 10.1515/cclm-2015-0766. Clin Chem Lab Med. 2016. PMID: 26581070

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