176 related articles for article (PubMed ID: 26180509)
1. 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]
2. Investigation of somatic NKX2-5 mutations in congenital heart disease.
Draus JM; Hauck MA; Goetsch M; Austin EH; Tomita-Mitchell A; Mitchell ME
J Med Genet; 2009 Feb; 46(2):115-22. PubMed ID: 19181906
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. Search of somatic GATA4 and NKX2.5 gene mutations in sporadic septal heart defects.
Salazar M; Consoli F; Villegas V; Caicedo V; Maddaloni V; Daniele P; Caianiello G; Pachón S; Nuñez F; Limongelli G; Pacileo G; Marino B; Bernal JE; De Luca A; Dallapiccola B
Eur J Med Genet; 2011; 54(3):306-9. PubMed ID: 21276881
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. [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]
9. 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]
10. Novel NKX2-5 mutations in diseased heart tissues of patients with cardiac malformations.
Reamon-Buettner SM; Hecker H; Spanel-Borowski K; Craatz S; Kuenzel E; Borlak J
Am J Pathol; 2004 Jun; 164(6):2117-25. PubMed ID: 15161646
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Investigation of somatic NKX2-5, GATA4 and HAND1 mutations in patients with tetralogy of Fallot.
Wang J; Lu Y; Chen H; Yin M; Yu T; Fu Q
Pathology; 2011 Jun; 43(4):322-6. PubMed ID: 21519287
[TBL] [Abstract][Full Text] [Related]
13. Sequence variations of NKX2-5 and HAND1 genes in patients with atrial isomerism.
Hatemi AC; Güleç C; Cine N; Vural B; Hatırnaz O; Sayitoğlu M; Oztunç F; Saltık L; Kansız E; Erginel Ünaltuna N
Anadolu Kardiyol Derg; 2011 Jun; 11(4):319-28. PubMed ID: 21561848
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. Somatic NKX2-5 mutations as a novel mechanism of disease in complex congenital heart disease.
Reamon-Buettner SM; Borlak J
J Med Genet; 2004 Sep; 41(9):684-90. PubMed ID: 15342699
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [Mutation of NKX2-5 gene in patients with atrial septal defect].
Liu XY; Yang YQ; Yang Y; Lin XP; Chen YH
Zhonghua Er Ke Za Zhi; 2009 Sep; 47(9):696-700. PubMed ID: 20021795
[TBL] [Abstract][Full Text] [Related]
20. Transcriptional defect of an inherited NKX2-5 haplotype comprising a SNP, a nonsynonymous and a synonymous mutation, associated with human congenital heart disease.
Reamon-Buettner SM; Sattlegger E; Ciribilli Y; Inga A; Wessel A; Borlak J
PLoS One; 2013; 8(12):e83295. PubMed ID: 24376681
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
