Association of NFKB1, NKX2-5, GATA4 and RANKL gene polymorphisms with sporadic congenital heart disease in Greek patients

1Zhang D, Li L, Zhu Y, Zhao L, Wan L, Lv J, et al. The NFKB1 -94 ATTG insertion/deletion polymorphism (rs28362491) contributes to the susceptibility of congenital heart disease in a Chinese population. Gene. 2013; 516(2): 307-310.Zhang D Li L Zhu Y Zhao L Wan L Lv J et al The NFKB1 -94 ATTG insertion/deletion polymorphism (rs28362491) contributes to the susceptibility of congenital heart disease in a Chinese population Gene 2013 516 2 307 31010.1016/j.gene.2012.12.07823299027Search in Google Scholar

2Pan Y, Wang ZG, Liu XY, Zhao H, Zhou N, Zheng GF, et al. A novel TBX1 loss-of-function mutation associated with congenital heart disease. Pediatr Cardiol. 2015; 36(7): 1400-1410.Pan Y Wang ZG Liu XY Zhao H Zhou N Zheng GF et al A novel TBX1 loss-of-function mutation associated with congenital heart disease Pediatr Cardiol 2015 36 7 1400 141010.1007/s00246-015-1173-x25860641Search in Google Scholar

3Tong YF. Mutations of NKX2.5 and GATA4 genes in the development of congenital heart disease. Gene. 2016; 588(1): 86-94.Tong YF Mutations of NKX2.5 and GATA4 genes in the development of congenital heart disease Gene 2016 588 1 86 9410.1016/j.gene.2016.04.06127154817Search in Google Scholar

4Chaix MA, Andelfinger G, Khairy P. Genetic testing in congenital heart disease: A clinical approach. World J Cardiol. 2016; 8(2): 180-191.Chaix MA Andelfinger G Khairy P Genetic testing in congenital heart disease: A clinical approach World J Cardiol 2016 8 2 180 19110.4330/wjc.v8.i2.180476626826981213Search in Google Scholar

5Cao Y, Wang J, Wei C, Hou Z, Li Y, Zou H, et al. Genetic variations of NKX2-5 in sporadic atrial septal defect and ventricular septal defect in Chinese Yunnan population. Gene. 2016; 575(1): 29-33.Cao Y Wang J Wei C Hou Z Li Y Zou H et al Genetic variations of NKX2-5 in sporadic atrial septal defect and ventricular septal defect in Chinese Yunnan population Gene 2016 575 1 29 3310.1016/j.gene.2015.08.03326297999Search in Google Scholar

6Su W, Zhu P, Wang R, Wu Q, Wang M, Zhang X, et al. Congenital heart diseases and their association with the variant distribution features on susceptibility genes. Clin Genet. 2017; 91(3): 349-354.Su W Zhu P Wang R Wu Q Wang M Zhang X et al Congenital heart diseases and their association with the variant distribution features on susceptibility genes Clin Genet 2017 91 3 349 35410.1111/cge.1283527426723Search in Google Scholar

7Wang Z, Zou L, Zhong R, Zhu B, Chen W, Shen N, et al. Associations between two genetic variants in NKX2-5 and risk of congenital heart disease in Chinese population: a meta-analysis. PLoS One. 2013; 8(8): e70979.Wang Z Zou L Zhong R Zhu B Chen W Shen N et al Associations between two genetic variants in NKX2-5 and risk of congenital heart disease in Chinese population: a meta-analysis PLoS One 2013 8 8 e7097910.1371/journal.pone.0070979373228723936479Search in Google Scholar

8Pulignani S, Vecoli C, Sabina S, Foffa I, Ait-Ali L, Andreassi MG. 3’UTR SNPs and haplotypes in the GATA4 gene contribute to the genetic risk of congenital heart disease. Rev Esp Cardiol (Engl Ed). 2016; 69(8): 760-765.Pulignani S Vecoli C Sabina S Foffa I Ait-Ali L Andreassi MG 3’UTR SNPs and haplotypes in the GATA4 gene contribute to the genetic risk of congenital heart disease Rev Esp Cardiol (Engl Ed) 2016 69 8 760 76510.1016/j.rec.2016.03.00427118528Search in Google Scholar

9Yang X, Li P, Tao J, Qin C, Cao Q, Gu J, et al. Association between NFKB1 -94ins/del ATTG promoter polymorphism and cancer susceptibility: An updated meta-analysis. Int J Genomics. 2014; 2014: 612972.Yang X Li P Tao J Qin C Cao Q Gu J et al Association between NFKB1 -94ins/del ATTG promoter polymorphism and cancer susceptibility: An updated meta-analysis Int J Genomics 2014 2014 61297210.1155/2014/612972403354724895544Search in Google Scholar

10Wang F, Wang H, Wang L, Zhou S, Chang M, Zhou J, et al. Association between single nucleotide polymorphisms in NFATC1 signaling pathway genes and susceptibility to congenital heart disease in the Chinese population. Pediatr Cardiol. 2016; 37(8): 1548-1561.Wang F Wang H Wang L Zhou S Chang M Zhou J et al Association between single nucleotide polymorphisms in NFATC1 signaling pathway genes and susceptibility to congenital heart disease in the Chinese population Pediatr Cardiol 2016 37 8 1548 156110.1007/s00246-016-1469-527567908Search in Google Scholar

11Yang J, Si D, Zhao Y, He C, Yang P. S-amlodipine improves endothelial dysfunction via the RANK/ RANKL/OPG system by regulating microRNA-155 in hypertension. Biomed Pharmacother. 2019; 114: 108799.Yang J Si D Zhao Y He C Yang P S-amlodipine improves endothelial dysfunction via the RANK/ RANKL/OPG system by regulating microRNA-155 in hypertension Biomed Pharmacother 2019 114 10879910.1016/j.biopha.2019.10879930951948Search in Google Scholar

12Chen B, Wu W, Sun W, Zhang Q, Yan F, Xiao Y. RANKL expression in periodontal disease: Where does RANKL come from? Biomed Res Int. 2014; 2014: 731039.Chen B Wu W Sun W Zhang Q Yan F Xiao Y RANKL expression in periodontal disease: Where does RANKL come from? Biomed Res Int 2014 2014 73103910.1155/2014/731039395560624719884Search in Google Scholar

13Bishop KA, Wang X, Coy HM, Meyer MB, Gumperz JE, Pike JW. Transcriptional regulation of the human TNFSF11 gene in T cells via a cell type-selective set of distal enhancers. J Cell Biochem. 2015; 116(2): 320-330.Bishop KA Wang X Coy HM Meyer MB Gumperz JE Pike JW Transcriptional regulation of the human TNFSF11 gene in T cells via a cell type-selective set of distal enhancers J Cell Biochem 2015 116 2 320 33010.1002/jcb.24974430334225211367Search in Google Scholar

14Sweeting MJ, Sutton AJ, Lambert PC. What to add to nothing? Use and avoidance of continuity corrections in meta-analysis of sparse data. Stat Med. 2004; 23(9): 1351-1375.Sweeting MJ Sutton AJ Lambert PC What to add to nothing? Use and avoidance of continuity corrections in meta-analysis of sparse data Stat Med 2004 23 9 1351 137510.1002/sim.176115116347Search in Google Scholar

15Cao Y, Lan W, Li Y, Wei C, Zou H, Jiang L. Single nucleotide polymorphism of NKX2-5 gene with sporadic congenital heart disease in Chinese Bai population. Int J Clin Exp Pathol. 2015; 8(11): 14917-1424.Cao Y Lan W Li Y Wei C Zou H Jiang L Single nucleotide polymorphism of NKX2-5 gene with sporadic congenital heart disease in Chinese Bai population Int J Clin Exp Pathol 2015 8 11 14917 1424Search in Google Scholar

16Lai HM, Li XM, Yang YN, Ma YT, Xu R, Pan S, et al. Genetic variation in NFKB1 and NFKBIA and susceptibility to coronary artery disease in a Chinese Uygur population. PLoS One. 2015; 10(6): e0129144.Lai HM Li XM Yang YN Ma YT Xu R Pan S et al Genetic variation in NFKB1 and NFKBIA and susceptibility to coronary artery disease in a Chinese Uygur population PLoS One 2015 10 6 e012914410.1371/journal.pone.0129144446807826075620Search in Google Scholar

17Vogel U, Jensen MK, Due KM, Rimm EB, Wallin H, Nielsen MR, et al. The NFKB1 ATTG ins/del polymorphism and risk of coronary heart disease in three independent populations. Atherosclerosis. 2011; 219(1): 200-204.Vogel U Jensen MK Due KM Rimm EB Wallin H Nielsen MR et al The NFKB1 ATTG ins/del polymorphism and risk of coronary heart disease in three independent populations Atherosclerosis 2011 219 1 200 20410.1016/j.atherosclerosis.2011.06.018382702221726863Search in Google Scholar

18Lo Iacono N, Pangrazio A, Abinun M, Bredius R, Zecca M, Blair HC, et al. RANKL cytokine: From pioneer of the osteoimmunology era to cure for a rare disease. Clin Dev Immunol. 2013; 2013: 412768.Lo Iacono N Pangrazio A Abinun M Bredius R Zecca M Blair HC et al RANKL cytokine: From pioneer of the osteoimmunology era to cure for a rare disease Clin Dev Immunol 2013 2013 41276810.1155/2013/412768367126623762088Search in Google Scholar

19Yang XY, Jing XY, Chen Z, Liu YL. Correlation between GATA4 gene polymorphism and congenital heart disease. Int J Clin Exp Med. 2015; 8(9): 1673316736.Yang XY Jing XY Chen Z Liu YL Correlation between GATA4 gene polymorphism and congenital heart disease Int J Clin Exp Med 2015 8 9 1673316736Search in Google Scholar

20Shi L, Shen AD, Li XF, Bai S, Guan XL, Li ZZ. Mutation screening of Nkx2.5 gene and association study in exon1 in Chinese with congenital heart disease. J Cap Univ Med Sci. 2005; 26(5): 525-528.Shi L Shen AD Li XF Bai S Guan XL Li ZZ Mutation screening of Nkx2.5 gene and association study in exon1 in Chinese with congenital heart disease J Cap Univ Med Sci 2005 26 5 525 528Search in Google Scholar

21Yin J, Qian J, Dai G, Wang C, Qin Y, Xu T, et al. Search of somatic mutations of NKX2-5 and GATA4 genes in Chinese patients with sporadic congenital heart disease. Pediatr Cardiol. 2019; 40(1): 17-22.Yin J Qian J Dai G Wang C Qin Y Xu T et al Search of somatic mutations of NKX2-5 and GATA4 genes in Chinese patients with sporadic congenital heart disease Pediatr Cardiol 2019 40 1 17 2210.1007/s00246-018-1955-z30121862Search in Google Scholar

22Zheng J, Li F, Liu J, Xu Z, Zhang H, Fu Q, et al. Investigation of somatic NKX2-5 mutations in Chinese children with congenital heart disease. Int J Med Sci. 2015; 12(7): 538-543.Zheng J Li F Liu J Xu Z Zhang H Fu Q et al Investigation of somatic NKX2-5 mutations in Chinese children with congenital heart disease Int J Med Sci 2015 12 7 538 54310.7150/ijms.11700450205726180509Search in Google Scholar