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No association of pri-miR-143 rs41291957 polymorphism with the risk of congenital heart disease in a Chinese population.

Yang L, Gao X, Luo H, Huang Q, Wei Y, Zhang G, Huang G, Su D, Chen L, Lu C, Yang J, Ma X.

Pediatr Cardiol. 2014 Aug;35(6):1057-61. doi: 10.1007/s00246-014-0898-2. Epub 2014 Apr 22.


No association of functional variant in pri-miR-218 and risk of congenital heart disease in a Chinese population.

Gao X, Yang L, Ma Y, Yang J, Zhang G, Huang G, Huang Q, Chen L, Fu F, Chen Y, Su D, Dong Y, Ma X, Lu C, Peng X.

Gene. 2013 Jul 10;523(2):173-7. doi: 10.1016/j.gene.2013.03.119. Epub 2013 Apr 6.


Single-nucleotide polymorphism of the pri-miR-34b/c gene is not associated with susceptibility to congenital heart disease in the Han Chinese population.

Liu YM, Wang Y, Peng W, Wu Z, Wang XH, Wang ML, Wang W, Sun J, Zhang ZD, Mo XM.

Genet Mol Res. 2013 Aug 12;12(3):2937-44. doi: 10.4238/2013.August.12.9.


Functional variant in microRNA-196a2 contributes to the susceptibility of congenital heart disease in a Chinese population.

Xu J, Hu Z, Xu Z, Gu H, Yi L, Cao H, Chen J, Tian T, Liang J, Lin Y, Qiu W, Ma H, Shen H, Chen Y.

Hum Mutat. 2009 Aug;30(8):1231-6. doi: 10.1002/humu.21044.


Association of two variants in SMAD7 with the risk of congenital heart disease in the Han Chinese population.

Wang E, Jin W, Duan W, Qiao B, Sun S, Huang G, Shi K, Jin L, Wang H.

PLoS One. 2013 Sep 5;8(9):e72423. doi: 10.1371/journal.pone.0072423. eCollection 2013.


A genetic variant in pre-miR-27a is associated with a reduced cervical cancer risk in southern Chinese women.

Xiong XD, Luo XP, Cheng J, Liu X, Li EM, Zeng LQ.

Gynecol Oncol. 2014 Feb;132(2):450-4. doi: 10.1016/j.ygyno.2013.12.030. Epub 2013 Dec 28.


Common variations in BMP4 confer genetic susceptibility to sporadic congenital heart disease in a Han Chinese population.

Qian B, Mo R, Da M, Peng W, Hu Y, Mo X.

Pediatr Cardiol. 2014 Dec;35(8):1442-7. doi: 10.1007/s00246-014-0951-1. Epub 2014 Jul 15.


ISL1 common variant rs1017 is not associated with susceptibility to congenital heart disease in a Chinese population.

Xue L, Wang X, Xu J, Xu X, Liu X, Hu Z, Shen H, Chen Y.

Genet Test Mol Biomarkers. 2012 Jul;16(7):679-83. doi: 10.1089/gtmb.2011.0249. Epub 2012 Apr 5.


Association Between Sequence Variations in RCAN1 Promoter and the Risk of Sporadic Congenital Heart Disease in a Chinese Population.

Li X, Wang G, An Y, Li H, Li Y, Wu C.

Pediatr Cardiol. 2015 Oct;36(7):1393-9. doi: 10.1007/s00246-015-1172-y. Epub 2015 Apr 12.


Polymorphisms involved in the miR-218-LAMB3 pathway and susceptibility of cervical cancer, a case-control study in Chinese women.

Zhou X, Chen X, Hu L, Han S, Qiang F, Wu Y, Pan L, Shen H, Li Y, Hu Z.

Gynecol Oncol. 2010 May;117(2):287-90. doi: 10.1016/j.ygyno.2010.01.020. Epub 2010 Feb 16.


Single nucleotide polymorphism of NKX2-5 gene with sporadic congenital heart disease in Chinese Bai population.

Cao Y, Lan W, Li Y, Wei C, Zou H, Jiang L.

Int J Clin Exp Pathol. 2015 Nov 1;8(11):14917-24. eCollection 2015.


Germline hereditary, somatic mutations and microRNAs targeting-SNPs in congenital heart defects.

Sabina S, Pulignani S, Rizzo M, Cresci M, Vecoli C, Foffa I, Ait-Ali L, Pitto L, Andreassi MG.

J Mol Cell Cardiol. 2013 Jul;60:84-9. doi: 10.1016/j.yjmcc.2013.04.002. Epub 2013 Apr 11.


Genetic variants of the endothelial NO synthase gene (eNOS) may confer increased risk of sporadic congenital heart disease.

Zhou K, Wang Y, Peng W, Sun J, Qing YM, Mo XM.

Genet Mol Res. 2014 May 16;13(2):3805-11. doi: 10.4238/2014.May.16.4.


Pri-miR-34b/c rs4938723 polymorphism contributes to acute lymphoblastic leukemia susceptibility in Chinese children.

Tong N, Chu H, Wang M, Xue Y, Du M, Lu L, Zhang H, Wang F, Fang Y, Li J, Wu D, Zhang Z, Sheng X.

Leuk Lymphoma. 2016;57(6):1436-41. doi: 10.3109/10428194.2015.1092528. Epub 2015 Nov 16.


Increased risk for congenital heart defects in children carrying the ABCB1 Gene C3435T polymorphism and maternal periconceptional toxicants exposure.

Wang C, Xie L, Zhou K, Zhan Y, Li Y, Li H, Qiao L, Wang F, Hua Y.

PLoS One. 2013 Jul 17;8(7):e68807. doi: 10.1371/journal.pone.0068807. Print 2013.


Relationship between polymorphism of cystathionine beta synthase gene and congenital heart disease in Chinese nuclear families.

Song XM, Zheng XY, Zhu WL, Huang L, Li Y.

Biomed Environ Sci. 2006 Dec;19(6):452-6.


Lack of association of the 3'-UTR polymorphism (rs1017) in the ISL1 gene and risk of congenital heart disease in the white population.

Cresci M, Vecoli C, Foffa I, Pulignani S, Ait-Ali L, Andreassi MG.

Pediatr Cardiol. 2013 Apr;34(4):938-41. doi: 10.1007/s00246-012-0578-z. Epub 2012 Nov 15.


A pri-miR-218 variant and risk of cervical carcinoma in Chinese women.

Shi TY, Chen XJ, Zhu ML, Wang MY, He J, Yu KD, Shao ZM, Sun MH, Zhou XY, Cheng X, Wu X, Wei Q.

BMC Cancer. 2013 Jan 15;13:19. doi: 10.1186/1471-2407-13-19.


A functional variant in microRNA-196a2 is associated with susceptibility of colorectal cancer in a Chinese population.

Zhan JF, Chen LH, Chen ZX, Yuan YW, Xie GZ, Sun AM, Liu Y.

Arch Med Res. 2011 Feb;42(2):144-8. doi: 10.1016/j.arcmed.2011.04.001.


A genetic variant in microRNA-122 regulatory region confers risk for chronic hepatitis B virus infection and hepatocellular carcinoma in Han Chinese.

Liu Y, Xie K, Wen J, Deng M, Li J, Hu Z.

J Med Virol. 2014 Oct;86(10):1669-74. doi: 10.1002/jmv.23996. Epub 2014 Jul 3.


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