Similar articles for PMID: 12414819

Year	Number of Results
1994	1
1997	1
1998	1
1999	3
2000	4
2001	3
2002	4
2003	4
2004	5
2005	4
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2008	8
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2010	6
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2013	4
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2022	2
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1

Two novel frameshift mutations in NKX2.5 result in novel features including visceral inversus and sinus venosus type ASD.

Watanabe Y, Benson DW, Yano S, Akagi T, Yoshino M, Murray JC. Watanabe Y, et al. J Med Genet. 2002 Nov;39(11):807-11. doi: 10.1136/jmg.39.11.807. J Med Genet. 2002. PMID: 12414819 Free PMC article. No abstract available.

2

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. Hirayama-Yamada K, et al. Am J Med Genet A. 2005 May 15;135(1):47-52. doi: 10.1002/ajmg.a.30684. Am J Med Genet A. 2005. PMID: 15810002

3

[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. Tian L, et al. Zhonghua Yi Xue Za Zhi. 2008 Jan 22;88(4):250-3. Zhonghua Yi Xue Za Zhi. 2008. PMID: 18361836 Chinese.

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. Elliott DA, et al. J Am Coll Cardiol. 2003 Jun 4;41(11):2072-6. doi: 10.1016/s0735-1097(03)00420-0. J Am Coll Cardiol. 2003. PMID: 12798584 Free article.

5

Spectrum of atrial septal defects associated with mutations of NKX2.5 and GATA4 transcription factors.

Sarkozy A, Conti E, Neri C, D'Agostino R, Digilio MC, Esposito G, Toscano A, Marino B, Pizzuti A, Dallapiccola B. Sarkozy A, et al. J Med Genet. 2005 Feb;42(2):e16. doi: 10.1136/jmg.2004.026740. J Med Genet. 2005. PMID: 15689439 Free PMC article. No abstract available.

6

NKX2.5 mutations in patients with congenital heart disease.

McElhinney DB, Geiger E, Blinder J, Benson DW, Goldmuntz E. McElhinney DB, et al. J Am Coll Cardiol. 2003 Nov 5;42(9):1650-5. doi: 10.1016/j.jacc.2003.05.004. J Am Coll Cardiol. 2003. PMID: 14607454 Free article.

7

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. Kasahara H, et al. J Clin Invest. 2000 Jul;106(2):299-308. doi: 10.1172/JCI9860. J Clin Invest. 2000. PMID: 10903346 Free PMC article.

8

Novel point mutation in the NKX2-5 gene in a Moroccan family with atrioventricular conduction disturbance and an atrial septal defect in the oval fossa.

Rifai L, Maazouzi W, Sefiani A. Rifai L, et al. Cardiol Young. 2007 Feb;17(1):107-9. doi: 10.1017/S1047951106001338. Epub 2006 Dec 22. Cardiol Young. 2007. PMID: 17184575

9

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. Schott JJ, et al. Science. 1998 Jul 3;281(5373):108-11. doi: 10.1126/science.281.5373.108. Science. 1998. PMID: 9651244

10

Cardiac septal and valvular dysmorphogenesis in mice heterozygous for mutations in the homeobox gene Nkx2-5.

Biben C, Weber R, Kesteven S, Stanley E, McDonald L, Elliott DA, Barnett L, Köentgen F, Robb L, Feneley M, Harvey RP. Biben C, et al. Circ Res. 2000 Nov 10;87(10):888-95. doi: 10.1161/01.res.87.10.888. Circ Res. 2000. PMID: 11073884

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