328 related articles for article (PubMed ID: 30344277)
1. 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]
2. Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome.
Elliott DA; Kirk EP; Yeoh T; Chandar S; McKenzie F; Taylor P; Grossfeld P; Fatkin D; Jones O; Hayes P; Feneley M; Harvey RP
J Am Coll Cardiol; 2003 Jun; 41(11):2072-6. PubMed ID: 12798584
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Novel Point Mutations of CITED2 Gene Are Associated with Non-familial Congenital Heart Disease (CHD) in Sporadic Pediatric Patients.
Dianatpour S; Khatami M; Heidari MM; Hadadzadeh M
Appl Biochem Biotechnol; 2020 Mar; 190(3):896-906. PubMed ID: 31515672
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. NKX2.5 mutations in patients with congenital heart disease.
McElhinney DB; Geiger E; Blinder J; Benson DW; Goldmuntz E
J Am Coll Cardiol; 2003 Nov; 42(9):1650-5. PubMed ID: 14607454
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. [NKX2.5 and TBX5 gene mutations in in vitro fertilization children with congenital heart disease].
Yang JH; Xu XY; Mi HY; Jiang Y; Ma XM; Li L
Zhongguo Dang Dai Er Ke Za Zhi; 2017 Jun; 19(6):652-657. PubMed ID: 28606231
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
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. 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]
18. 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]
19. 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]
20. 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]
[Next] [New Search]