141 related articles for article (PubMed ID: 21262546)
1. Identifying novel mutations of NKX2-5 congenital heart disease patients of Chinese minority groups.
Wang J; Chen Q; Wang L; Zhou S; Cheng L; Xie X; Huang G; Wang B; Ma X
Int J Cardiol; 2011 Apr; 148(1):102-4. PubMed ID: 21262546
[No Abstract] [Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. A mouse model of human congenital heart disease: high incidence of diverse cardiac anomalies and ventricular noncompaction produced by heterozygous Nkx2-5 homeodomain missense mutation.
Ashraf H; Pradhan L; Chang EI; Terada R; Ryan NJ; Briggs LE; Chowdhury R; Zárate MA; Sugi Y; Nam HJ; Benson DW; Anderson RH; Kasahara H
Circ Cardiovasc Genet; 2014 Aug; 7(4):423-433. PubMed ID: 25028484
[TBL] [Abstract][Full Text] [Related]
10. 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]
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. 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]
13. Biochemical analyses of eight NKX2.5 homeodomain missense mutations causing atrioventricular block and cardiac anomalies.
Kasahara H; Benson DW
Cardiovasc Res; 2004 Oct; 64(1):40-51. PubMed ID: 15364612
[TBL] [Abstract][Full Text] [Related]
14. [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]
15. [Genetic screening of Gata4 and Nkx2.5 mutations in hereditary congenital heart defects: 5 familial cases].
Pulignani S; Foffa I; Cresci M; Vittorini S; Ait-Ali L; Andreassi MG
Recenti Prog Med; 2011 Mar; 102(3):120-5. PubMed ID: 21572484
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. NKX2.5 and congenital heart defects: A population-based study.
Hobbs CA; Cleves MA; Keith C; Ghaffar S; James SJ
Am J Med Genet A; 2005 Apr; 134A(2):223-5. PubMed ID: 15633194
[No Abstract] [Full Text] [Related]
18. NKX2-5 mutations in an inbred consanguineous population: genetic and phenotypic diversity.
Abou Hassan OK; Fahed AC; Batrawi M; Arabi M; Refaat MM; DePalma SR; Seidman JG; Seidman CE; Bitar FF; Nemer GM
Sci Rep; 2015 Mar; 5():8848. PubMed ID: 25742962
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Homeodomain factor Nkx2-5 in heart development and disease.
Harvey RP; Lai D; Elliott D; Biben C; Solloway M; Prall O; Stennard F; Schindeler A; Groves N; Lavulo L; Hyun C; Yeoh T; Costa M; Furtado M; Kirk E
Cold Spring Harb Symp Quant Biol; 2002; 67():107-14. PubMed ID: 12858530
[No Abstract] [Full Text] [Related]
[Next] [New Search]
