Yang YQ - 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: yang yq. 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

KCNQ1 gain-of-function mutation in familial atrial fibrillation.

Chen YH, Xu SJ, Bendahhou S, Wang XL, Wang Y, Xu WY, Jin HW, Sun H, Su XY, Zhuang QN, Yang YQ, Li YB, Liu Y, Xu HJ, Li XF, Ma N, Mou CP, Chen Z, Barhanin J, Huang W. Chen YH, et al. Among authors: yang yq. Science. 2003 Jan 10;299(5604):251-4. doi: 10.1126/science.1077771. Science. 2003. PMID: 12522251

3

Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation.

Yang Y, Xia M, Jin Q, Bendahhou S, Shi J, Chen Y, Liang B, Lin J, Liu Y, Liu B, Zhou Q, Zhang D, Wang R, Ma N, Su X, Niu K, Pei Y, Xu W, Chen Z, Wan H, Cui J, Barhanin J, Chen Y. Yang Y, et al. Am J Hum Genet. 2004 Nov;75(5):899-905. doi: 10.1086/425342. Epub 2004 Sep 13. Am J Hum Genet. 2004. PMID: 15368194 Free PMC article.

4

KCNE3 R53H substitution in familial atrial fibrillation.

Zhang DF, Liang B, Lin J, Liu B, Zhou QS, Yang YQ. Zhang DF, et al. Among authors: yang yq. Chin Med J (Engl). 2005 Oct 20;118(20):1735-8. Chin Med J (Engl). 2005. PMID: 16313760 No abstract available.

5

Novel KCNA5 loss-of-function mutations responsible for atrial fibrillation.

Yang Y, Li J, Lin X, Yang Y, Hong K, Wang L, Liu J, Li L, Yan D, Liang D, Xiao J, Jin H, Wu J, Zhang Y, Chen YH. Yang Y, et al. J Hum Genet. 2009 May;54(5):277-83. doi: 10.1038/jhg.2009.26. Epub 2009 Apr 3. J Hum Genet. 2009. PMID: 19343045

6

[Identification and functional analysis of a KCNA5 mutation responsible for idiopathic atrial fibrillation].

Yang YQ, Lin XP, Li J, Chen YH. Yang YQ, et al. Zhonghua Yi Xue Za Zhi. 2010 Apr 27;90(16):1100-4. Zhonghua Yi Xue Za Zhi. 2010. PMID: 20646426 Chinese.

7

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. Europace. 2010 Oct;12(10):1421-7. doi: 10.1093/europace/euq274. Epub 2010 Jul 21. Europace. 2010. PMID: 20650941

8

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. Int J Mol Med. 2010 Oct;26(4):605-10. doi: 10.3892/ijmm_00000505. Int J Mol Med. 2010. PMID: 20818502

9

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. Intern Med. 2010;49(22):2385-91. doi: 10.2169/internalmedicine.49.4130. Epub 2010 Nov 15. Intern Med. 2010. PMID: 21088338 Free article.

10

A novel NKX2-5 mutation in familial ventricular septal defect.

Wang J, Xin YF, Liu XY, Liu ZM, Wang XZ, Yang YQ. Wang J, et al. Among authors: yang yq. Int J Mol Med. 2011 Mar;27(3):369-75. doi: 10.3892/ijmm.2010.585. Epub 2010 Dec 16. Int J Mol Med. 2011. PMID: 21165553

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