246 related articles for article (PubMed ID: 12112663)
1. Progressive AV-block and anomalous venous return among cardiac anomalies associated with two novel missense mutations in the CSX/NKX2-5 gene.
Gutierrez-Roelens I; Sluysmans T; Gewillig M; Devriendt K; Vikkula M
Hum Mutat; 2002 Jul; 20(1):75-6. PubMed ID: 12112663
[TBL] [Abstract][Full Text] [Related]
2. A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype?
Gutierrez-Roelens I; De Roy L; Ovaert C; Sluysmans T; Devriendt K; Brunner HG; Vikkula M
Eur J Hum Genet; 2006 Dec; 14(12):1313-6. PubMed ID: 16896344
[TBL] [Abstract][Full Text] [Related]
3. Novel point mutation in the cardiac transcription factor CSX/NKX2.5 associated with congenital heart disease.
Ikeda Y; Hiroi Y; Hosoda T; Utsunomiya T; Matsuo S; Ito T; Inoue J; Sumiyoshi T; Takano H; Nagai R; Komuro I
Circ J; 2002 Jun; 66(6):561-3. PubMed ID: 12074273
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Progressive atrioventricular conduction defects and heart failure in mice expressing a mutant Csx/Nkx2.5 homeoprotein.
Kasahara H; Wakimoto H; Liu M; Maguire CT; Converso KL; Shioi T; Huang WY; Manning WJ; Paul D; Lawitts J; Berul CI; Izumo S
J Clin Invest; 2001 Jul; 108(2):189-201. PubMed ID: 11457872
[TBL] [Abstract][Full Text] [Related]
7. Familial atrial septal defect and atrioventricular conduction disturbance associated with a point mutation in the cardiac homeobox gene CSX/NKX2-5 in a Japanese patient.
Hosoda T; Komuro I; Shiojima I; Hiroi Y; Harada M; Murakawa Y; Hirata Y; Yazaki Y
Jpn Circ J; 1999 May; 63(5):425-6. PubMed ID: 10943630
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect.
Hirayama-Yamada K; Kamisago M; Akimoto K; Aotsuka H; Nakamura Y; Tomita H; Furutani M; Imamura S; Takao A; Nakazawa M; Matsuoka R
Am J Med Genet A; 2005 May; 135(1):47-52. PubMed ID: 15810002
[TBL] [Abstract][Full Text] [Related]
10. Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways.
Benson DW; Silberbach GM; Kavanaugh-McHugh A; Cottrill C; Zhang Y; Riggs S; Smalls O; Johnson MC; Watson MS; Seidman JG; Seidman CE; Plowden J; Kugler JD
J Clin Invest; 1999 Dec; 104(11):1567-73. PubMed ID: 10587520
[TBL] [Abstract][Full Text] [Related]
11. 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]
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. [Gene mutation in secundum atrial septal defect: analysis of a Chinese family with 3 patients].
Tian L; Zhu JF; Yang JG; Zhu QH; Du R; Li J; Li W
Zhonghua Yi Xue Za Zhi; 2008 Jan; 88(4):250-3. PubMed ID: 18361836
[TBL] [Abstract][Full Text] [Related]
14. Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease.
Kasahara H; Lee B; Schott JJ; Benson DW; Seidman JG; Seidman CE; Izumo S
J Clin Invest; 2000 Jul; 106(2):299-308. PubMed ID: 10903346
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Cardiac transcription factor Csx/Nkx2-5: Its role in cardiac development and diseases.
Akazawa H; Komuro I
Pharmacol Ther; 2005 Aug; 107(2):252-68. PubMed ID: 15925411
[TBL] [Abstract][Full Text] [Related]
17. A novel stop mutation truncating critical regions of the cardiac transcription factor NKX2-5 in a large family with autosomal-dominant inherited congenital heart disease.
Pabst S; Wollnik B; Rohmann E; Hintz Y; Glänzer K; Vetter H; Nickenig G; Grohé C
Clin Res Cardiol; 2008 Jan; 97(1):39-42. PubMed ID: 17891520
[TBL] [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. 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]
20. Congenital heart disease caused by mutations in the transcription factor NKX2-5.
Schott JJ; Benson DW; Basson CT; Pease W; Silberbach GM; Moak JP; Maron BJ; Seidman CE; Seidman JG
Science; 1998 Jul; 281(5373):108-11. PubMed ID: 9651244
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]