Li RG - Search Results

1

Detection and functional characterization of a novel MEF2A variation responsible for familial dilated cardiomyopathy.

Qiao Q, Zhao CM, Yang CX, Gu JN, Guo YH, Zhang M, Li RG, Qiu XB, Xu YJ, Yang YQ. Qiao Q, et al. Among authors: li rg. Clin Chem Lab Med. 2020 Dec 3;59(5):955-963. doi: 10.1515/cclm-2020-1318. Print 2021 Apr 27. Clin Chem Lab Med. 2020. PMID: 33554560

2

Transcatheter coil embolization of multiple coronary artery-to-left ventricle fistulas: report of a rare case.

Li RG, Fang WY, Shi HY, Qu XK, Chen H, Qiu XB, Xu YJ, Dong JL, Guan SF, Jiang B, Wu WH. Li RG, et al. Chin Med J (Engl). 2008 Jul 20;121(14):1342-4. Chin Med J (Engl). 2008. PMID: 18713560 No abstract available.

3

Acute and chronic myocardial infarction in a pig model: utility of multi-slice cardiac computed tomography in assessing myocardial viability and infarct parameters.

Qu X, Fang W, Ye J, Koh AS, Xu Y, Guan S, Li R, Shen Y. Qu X, et al. Eur J Radiol. 2012 Apr;81(4):e431-7. doi: 10.1016/j.ejrad.2011.03.062. Epub 2011 May 6. Eur J Radiol. 2012. PMID: 21550194

4

GATA6 loss-of-function mutation in atrial fibrillation.

Yang YQ, Li L, Wang J, Zhang XL, Li RG, Xu YJ, Tan HW, Wang XH, Jiang JQ, Fang WY, Liu X. Yang YQ, et al. Among authors: li rg, li l. Eur J Med Genet. 2012 Oct;55(10):520-6. doi: 10.1016/j.ejmg.2012.06.007. Epub 2012 Jun 26. Eur J Med Genet. 2012. PMID: 22750565

5

Novel GATA6 mutations associated with congenital ventricular septal defect or tetralogy of fallot.

Wang J, Luo XJ, Xin YF, Liu Y, Liu ZM, Wang Q, Li RG, Fang WY, Wang XZ, Yang YQ. Wang J, et al. Among authors: li rg. DNA Cell Biol. 2012 Nov;31(11):1610-7. doi: 10.1089/dna.2012.1814. Epub 2012 Sep 28. DNA Cell Biol. 2012. PMID: 23020118 Free PMC article.

6

Prevalence and spectrum of GATA5 mutations associated with congenital heart disease.

Jiang JQ, Li RG, Wang J, Liu XY, Xu YJ, Fang WY, Chen XZ, Zhang W, Wang XZ, Yang YQ. Jiang JQ, et al. Among authors: li rg. Int J Cardiol. 2013 May 25;165(3):570-3. doi: 10.1016/j.ijcard.2012.09.039. Epub 2012 Sep 30. Int J Cardiol. 2013. PMID: 23031282 No abstract available.

7

A novel GATA5 loss-of-function mutation underlies lone atrial fibrillation.

Wang XH, Huang CX, Wang Q, Li RG, Xu YJ, Liu X, Fang WY, Yang YQ. Wang XH, et al. Among authors: li rg. Int J Mol Med. 2013 Jan;31(1):43-50. doi: 10.3892/ijmm.2012.1189. Epub 2012 Nov 20. Int J Mol Med. 2013. PMID: 23175127

8

GATA5 loss-of-function mutations underlie tetralogy of fallot.

Wei D, Bao H, Liu XY, Zhou N, Wang Q, Li RG, Xu YJ, Yang YQ. Wei D, et al. Among authors: li rg. Int J Med Sci. 2013;10(1):34-42. doi: 10.7150/ijms.5270. Epub 2012 Dec 10. Int J Med Sci. 2013. PMID: 23289003 Free PMC article.

9

Prevalence and spectrum of GJA5 mutations associated with lone atrial fibrillation.

Shi HF, Yang JF, Wang Q, Li RG, Xu YJ, Qu XK, Fang WY, Liu X, Yang YQ. Shi HF, et al. Among authors: li rg. Mol Med Rep. 2013 Mar;7(3):767-74. doi: 10.3892/mmr.2012.1252. Epub 2012 Dec 28. Mol Med Rep. 2013. PMID: 23292621

10

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. 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

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