Liu X - Search Results

1

Mutations of the SCN4B-encoded sodium channel β4 subunit in familial atrial fibrillation.

Li RG, Wang Q, Xu YJ, Zhang M, Qu XK, Liu X, Fang WY, Yang YQ. Li RG, et al. Among authors: liu x. Int J Mol Med. 2013 Jul;32(1):144-50. doi: 10.3892/ijmm.2013.1355. Epub 2013 Apr 22. Int J Mol Med. 2013. PMID: 23604097

2

Novel connexin40 missense mutations in patients with familial atrial fibrillation.

Yang YQ, Liu X, Zhang XL, Wang XH, Tan HW, Shi HF, Jiang WF, Fang WY. Yang YQ, et al. Among authors: liu x. Europace. 2010 Oct;12(10):1421-7. doi: 10.1093/europace/euq274. Epub 2010 Jul 21. Europace. 2010. PMID: 20650941

3

Connexin40 nonsense mutation in familial atrial fibrillation.

Yang YQ, Zhang XL, Wang XH, Tan HW, Shi HF, Jiang WF, Fang WY, Liu X. Yang YQ, et al. Among authors: liu x. Int J Mol Med. 2010 Oct;26(4):605-10. doi: 10.3892/ijmm_00000505. Int J Mol Med. 2010. PMID: 20818502

4

Familial aggregation of lone atrial fibrillation in the Chinese population.

Yang YQ, Zhang XL, Wang XH, Tan HW, Shi HF, Fang WY, Liu X. Yang YQ, et al. Among authors: liu x. Intern Med. 2010;49(22):2385-91. doi: 10.2169/internalmedicine.49.4130. Epub 2010 Nov 15. Intern Med. 2010. PMID: 21088338 Free article.

5

Involvement of a novel GATA4 mutation in atrial septal defects.

Liu XY, Wang J, Zheng JH, Bai K, Liu ZM, Wang XZ, Liu X, Fang WY, Yang YQ. Liu XY, et al. Among authors: liu zm, liu x. Int J Mol Med. 2011 Jul;28(1):17-23. doi: 10.3892/ijmm.2011.638. Epub 2011 Mar 3. Int J Mol Med. 2011. PMID: 21373748

6

A novel GATA4 mutation responsible for congenital ventricular septal defects.

Wang J, Fang M, Liu XY, Xin YF, Liu ZM, Chen XZ, Wang XZ, Fang WY, Liu X, Yang YQ. Wang J, et al. Among authors: liu xy, liu zm, liu x. Int J Mol Med. 2011 Oct;28(4):557-64. doi: 10.3892/ijmm.2011.715. Epub 2011 Jun 1. Int J Mol Med. 2011. PMID: 21637914

7

GATA4 loss-of-function mutations in familial atrial fibrillation.

Yang YQ, Wang MY, Zhang XL, Tan HW, Shi HF, Jiang WF, Wang XH, Fang WY, Liu X. Yang YQ, et al. Among authors: liu x. Clin Chim Acta. 2011 Sep 18;412(19-20):1825-30. doi: 10.1016/j.cca.2011.06.017. Epub 2011 Jun 25. Clin Chim Acta. 2011. PMID: 21708142

8

Novel GATA4 mutations in lone atrial fibrillation.

Jiang JQ, Shen FF, Fang WY, Liu X, Yang YQ. Jiang JQ, et al. Among authors: liu x. Int J Mol Med. 2011 Dec;28(6):1025-32. doi: 10.3892/ijmm.2011.783. Epub 2011 Aug 26. Int J Mol Med. 2011. PMID: 21874226

9

A novel GATA4 loss-of-function mutation associated with congenital ventricular septal defect.

Yang YQ, Li L, Wang J, Liu XY, Chen XZ, Zhang W, Wang XZ, Jiang JQ, Liu X, Fang WY. Yang YQ, et al. Among authors: liu xy, liu x. Pediatr Cardiol. 2012 Apr;33(4):539-46. doi: 10.1007/s00246-011-0146-y. Epub 2011 Nov 20. Pediatr Cardiol. 2012. PMID: 22101736

10

Prevalence and spectrum of GATA6 mutations associated with familial atrial fibrillation.

Yang YQ, Wang XH, Tan HW, Jiang WF, Fang WY, Liu X. Yang YQ, et al. Among authors: liu x. Int J Cardiol. 2012 Mar 22;155(3):494-6. doi: 10.1016/j.ijcard.2011.12.091. Epub 2012 Jan 16. Int J Cardiol. 2012. PMID: 22257684 No abstract available.

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