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Results: 1 to 20 of 143

Related Citations for PubMed (Select 20659440)

1.

A novel mutation of GATA4 in a familial atrial septal defect.

Chen Y, Mao J, Sun Y, Zhang Q, Cheng HB, Yan WH, Choy KW, Li H.

Clin Chim Acta. 2010 Nov 11;411(21-22):1741-5. doi: 10.1016/j.cca.2010.07.021. Epub 2010 Jul 24.

PMID:
20659440
2.

A novel mutation in GATA4 gene associated with dominant inherited familial atrial septal defect.

Chen Y, Han ZQ, Yan WD, Tang CZ, Xie JY, Chen H, Hu DY.

J Thorac Cardiovasc Surg. 2010 Sep;140(3):684-7. doi: 10.1016/j.jtcvs.2010.01.013. Epub 2010 Mar 26.

PMID:
20347099
3.

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 15;135(1):47-52.

PMID:
15810002
4.

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.

J Med Genet. 2005 Feb;42(2):e16. No abstract available.

5.

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. doi: 10.1007/s10709-010-9522-4. Epub 2010 Nov 26.

PMID:
21110066
6.

Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects.

Posch MG, Perrot A, Schmitt K, Mittelhaus S, Esenwein EM, Stiller B, Geier C, Dietz R, Gessner R, Ozcelik C, Berger F.

Am J Med Genet A. 2008 Jan 15;146A(2):251-3. No abstract available.

PMID:
18076106
7.

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 20;122(4):416-9.

PMID:
19302747
8.

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. Epub 2007 Sep 25.

PMID:
17891520
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 Mar-Apr;22(2):141-5. doi: 10.1016/j.carpath.2012.07.001. Epub 2012 Sep 6.

PMID:
22959235
10.

Genetic screening of 104 patients with congenitally malformed hearts revealed a fresh mutation of GATA4 in those with atrial septal defects.

Hamanoue H, Rahayuningsih SE, Hirahara Y, Itoh J, Yokoyama U, Mizuguchi T, Saitsu H, Miyake N, Hirahara F, Matsumoto N.

Cardiol Young. 2009 Sep;19(5):482-5. doi: 10.1017/S1047951109990813. Epub 2009 Aug 13.

PMID:
19678963
11.

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. doi: 10.1111/j.1399-0004.2010.01422.x.

PMID:
20456451
12.

Investigation of somatic NKX2-5 mutations in congenital heart disease.

Draus JM Jr, Hauck MA, Goetsch M, Austin EH 3rd, Tomita-Mitchell A, Mitchell ME.

J Med Genet. 2009 Feb;46(2):115-22. doi: 10.1136/jmg.2008.060277.

13.

[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. doi: 10.1701/608.7068. Italian.

PMID:
21572484
14.

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 4;41(11):2072-6.

PMID:
12798584
15.

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 May-Jun;54(3):306-9. doi: 10.1016/j.ejmg.2011.01.004. Epub 2011 Jan 27.

PMID:
21276881
16.
17.

GATA4 mutations in Chinese patients with congenital cardiac septal defects.

Chen MW, Pang YS, Guo Y, Pan JH, Liu BL, Shen J, Liu TW.

Pediatr Cardiol. 2010 Jan;31(1):85-9. doi: 10.1007/s00246-009-9576-1. Epub 2009 Nov 14.

PMID:
19915893
18.

Novel NKX2-5 mutations in patients with familial atrial septal defects.

Liu XY, Wang J, Yang YQ, Zhang YY, Chen XZ, Zhang W, Wang XZ, Zheng JH, Chen YH.

Pediatr Cardiol. 2011 Feb;32(2):193-201. doi: 10.1007/s00246-010-9859-6. Epub 2010 Dec 25.

PMID:
21188375
19.

A novel mutation of GATA4 (K319E) is responsible for familial atrial septal defect and pulmonary valve stenosis.

Xiang R, Fan LL, Huang H, Cao BB, Li XP, Peng DQ, Xia K.

Gene. 2014 Jan 25;534(2):320-3.

PMID:
24498650
20.

[Novel GATA4 mutations identified in patients with congenital atrial septal defects].

Liu XY, Yang YQ, Ma J, Lin XP, Zheng JH, Bai K, Chen YH.

Zhonghua Xin Xue Guan Bing Za Zhi. 2010 Aug;38(8):724-7. Chinese.

PMID:
21055141
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