170 related articles for article (PubMed ID: 26823822)
1. 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; 8(11):14917-24. PubMed ID: 26823822
[TBL] [Abstract][Full Text] [Related]
2. Genetic variations of NKX2-5 in sporadic atrial septal defect and ventricular septal defect in Chinese Yunnan population.
Cao Y; Wang J; Wei C; Hou Z; Li Y; Zou H; Meng M; Wang W; Jiang L
Gene; 2016 Jan; 575(1):29-33. PubMed ID: 26297999
[TBL] [Abstract][Full Text] [Related]
3. Investigation of Somatic NKX2-5 Mutations in Chinese Children with Congenital Heart Disease.
Zheng J; Li F; Liu J; Xu Z; Zhang H; Fu Q; Wang J; Sun K
Int J Med Sci; 2015; 12(7):538-43. PubMed ID: 26180509
[TBL] [Abstract][Full Text] [Related]
4. Analyses of GATA4, NKX2.5, and TFAP2B genes in subjects from southern China with sporadic congenital heart disease.
Xiong F; Li Q; Zhang C; Chen Y; Li P; Wei X; Li Q; Zhou W; Li L; Shang X; Xu X
Cardiovasc Pathol; 2013; 22(2):141-5. PubMed ID: 22959235
[TBL] [Abstract][Full Text] [Related]
5. Screening NKX2.5 mutation in a sample of 230 Han Chinese children with congenital heart diseases.
Zhang W; Li X; Shen A; Jiao W; Guan X; Li Z
Genet Test Mol Biomarkers; 2009 Apr; 13(2):159-62. PubMed ID: 19371212
[TBL] [Abstract][Full Text] [Related]
6. GATA4 and NKX2.5 gene analysis in Chinese Uygur patients with congenital heart disease.
Zhang WM; Li XF; Ma ZY; Zhang J; Zhou SH; Li T; Shi L; Li ZZ
Chin Med J (Engl); 2009 Feb; 122(4):416-9. PubMed ID: 19302747
[TBL] [Abstract][Full Text] [Related]
7. Association of NKX2-5, GATA4, and TBX5 polymorphisms with congenital heart disease in Egyptian children.
Behiry EG; Al-Azzouny MA; Sabry D; Behairy OG; Salem NE
Mol Genet Genomic Med; 2019 May; 7(5):e612. PubMed ID: 30834692
[TBL] [Abstract][Full Text] [Related]
8. Novel NKX2-5 mutations responsible for congenital heart disease.
Wang J; Liu XY; Yang YQ
Genet Mol Res; 2011 Nov; 10(4):2905-15. PubMed ID: 22179962
[TBL] [Abstract][Full Text] [Related]
9. Association of functional variant in GDF1 promoter with risk of congenital heart disease and its regulation by Nkx2.5.
Gao X; Zheng P; Yang L; Luo H; Zhang C; Qiu Y; Huang G; Sheng W; Ma X; Lu C
Clin Sci (Lond); 2019 Jun; 133(12):1281-1295. PubMed ID: 31171573
[TBL] [Abstract][Full Text] [Related]
10. Investigation of NKX2.5 gene mutations in congenital heart defects in an Indian population.
Ketharnathan S; Koshy T; Sethuratnam R; Paul S; Venkatesan V
Genet Test Mol Biomarkers; 2015 Oct; 19(10):579-83. PubMed ID: 26273787
[TBL] [Abstract][Full Text] [Related]
11. Prevalence and spectrum of Nkx2.6 mutations in patients with congenital heart disease.
Zhao L; Ni SH; Liu XY; Wei D; Yuan F; Xu L; Xin-Li ; Li RG; Qu XK; Xu YJ; Fang WY; Yang YQ; Qiu XB
Eur J Med Genet; 2014 Oct; 57(10):579-86. PubMed ID: 25195019
[TBL] [Abstract][Full Text] [Related]
12. R25C mutation in the NKX2.5 gene in Italian patients affected with non-syndromic and syndromic congenital heart disease.
Beffagna G; Cecchetto A; Dal Bianco L; Lorenzon A; Angelini A; Padalino M; Vida V; Bhattacharya S; Stellin G; Rampazzo A; Daliento L
J Cardiovasc Med (Hagerstown); 2013 Aug; 14(8):582-6. PubMed ID: 22964646
[TBL] [Abstract][Full Text] [Related]
13. Search of Somatic Mutations of NKX2-5 and GATA4 Genes in Chinese Patients with Sporadic Congenital Heart Disease.
Yin J; Qian J; Dai G; Wang C; Qin Y; Xu T; Li Z; Zhang H; Yang S
Pediatr Cardiol; 2019 Jan; 40(1):17-22. PubMed ID: 30121862
[TBL] [Abstract][Full Text] [Related]
14. Novel Point Mutations in the
Khatami M; Mazidi M; Taher S; Heidari MM; Hadadzadeh M
Medicina (Kaunas); 2018 Jun; 54(3):. PubMed ID: 30344277
[No Abstract] [Full Text] [Related]
15. [Preliminary exploration of transcription factor Nkx2.5 mutations and congenital heart diseases].
Ding JD; Li KR; Zhang XL; Yao YY; Reng LQ; Tao SY; Fang X; Ma GS
Zhonghua Yi Xue Za Zhi; 2009 Apr; 89(16):1114-6. PubMed ID: 19595143
[TBL] [Abstract][Full Text] [Related]
16. Associations between two genetic variants in NKX2-5 and risk of congenital heart disease in Chinese population: a meta-analysis.
Wang Z; Zou L; Zhong R; Zhu B; Chen W; Shen N; Ke J; Lou J; Song R; Miao XP
PLoS One; 2013; 8(8):e70979. PubMed ID: 23936479
[TBL] [Abstract][Full Text] [Related]
17. Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease.
Stallmeyer B; Fenge H; Nowak-Göttl U; Schulze-Bahr E
Clin Genet; 2010 Dec; 78(6):533-40. PubMed ID: 20456451
[TBL] [Abstract][Full Text] [Related]
18. Mutations of the GATA4 and NKX2.5 genes in Chinese pediatric patients with non-familial congenital heart disease.
Peng T; Wang L; Zhou SF; Li X
Genetica; 2010 Dec; 138(11-12):1231-40. PubMed ID: 21110066
[TBL] [Abstract][Full Text] [Related]
19. Single-nucleotide polymorphisms of NKX2.5 found in congenital heart disease patients of Mysore, South India.
Dinesh SM; Kusuma L; Smitha R; Savitha MR; Krishnamurthy B; Narayanappa D; Ramachandra NB
Genet Test Mol Biomarkers; 2010 Dec; 14(6):873-9. PubMed ID: 21091212
[TBL] [Abstract][Full Text] [Related]
20. NKX2-5: an update on this hypermutable homeodomain protein and its role in human congenital heart disease (CHD).
Reamon-Buettner SM; Borlak J
Hum Mutat; 2010 Nov; 31(11):1185-94. PubMed ID: 20725931
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
