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Items: 1 to 20 of 125

1.

Identification of GATA6 sequence variants in patients with congenital heart defects.

Maitra M, Koenig SN, Srivastava D, Garg V.

Pediatr Res. 2010 Oct;68(4):281-5. doi: 10.1203/00006450-201011001-00549.

2.

Genetic analysis of essential cardiac transcription factors in 256 patients with non-syndromic congenital heart defects.

Kodo K, Nishizawa T, Furutani M, Arai S, Ishihara K, Oda M, Makino S, Fukuda K, Takahashi T, Matsuoka R, Nakanishi T, Yamagishi H.

Circ J. 2012;76(7):1703-11. Epub 2012 Apr 13.

3.

Novel GATA6 mutations associated with congenital ventricular septal defect or tetralogy of fallot.

Wang J, Luo XJ, Xin YF, Liu Y, Liu ZM, Wang Q, Li RG, Fang WY, Wang XZ, Yang YQ.

DNA Cell Biol. 2012 Nov;31(11):1610-7. doi: 10.1089/dna.2012.1814. Epub 2012 Sep 28.

4.

A novel GATA6 mutation associated with congenital ventricular septal defect.

Zheng GF, Wei D, Zhao H, Zhou N, Yang YQ, Liu XY.

Int J Mol Med. 2012 Jun;29(6):1065-71. doi: 10.3892/ijmm.2012.930. Epub 2012 Mar 7.

PMID:
22407241
5.

Somatic mutations in the GATA6 gene underlie sporadic tetralogy of Fallot.

Huang RT, Xue S, Xu YJ, Yang YQ.

Int J Mol Med. 2013 Jan;31(1):51-8. doi: 10.3892/ijmm.2012.1188. Epub 2012 Nov 20.

PMID:
23175051
6.

Identification of two novel GATA6 mutations in patients with nonsyndromic conotruncal heart defects.

Wang X, Ji W, Wang J, Zhao P, Guo Y, Xu R, Chen S, Sun K.

Mol Med Rep. 2014 Aug;10(2):743-8. doi: 10.3892/mmr.2014.2247. Epub 2014 May 16.

PMID:
24841381
7.

GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling.

Kodo K, Nishizawa T, Furutani M, Arai S, Yamamura E, Joo K, Takahashi T, Matsuoka R, Yamagishi H.

Proc Natl Acad Sci U S A. 2009 Aug 18;106(33):13933-8. doi: 10.1073/pnas.0904744106. Epub 2009 Aug 4.

8.

Interaction of Gata4 and Gata6 with Tbx5 is critical for normal cardiac development.

Maitra M, Schluterman MK, Nichols HA, Richardson JA, Lo CW, Srivastava D, Garg V.

Dev Biol. 2009 Feb 15;326(2):368-77. doi: 10.1016/j.ydbio.2008.11.004. Epub 2008 Nov 20.

9.

GATA5 interacts with GATA4 and GATA6 in outflow tract development.

Laforest B, Nemer M.

Dev Biol. 2011 Oct 15;358(2):368-78. doi: 10.1016/j.ydbio.2011.07.037. Epub 2011 Aug 4.

10.

Novel and functional DNA sequence variants within the GATA6 gene promoter in ventricular septal defects.

Li C, Li X, Pang S, Chen W, Qin X, Huang W, Zeng C, Yan B.

Int J Mol Sci. 2014 Jul 17;15(7):12677-87. doi: 10.3390/ijms150712677.

11.

Downregulation of GATA4 and GATA6 in the heart of rats with nitrofen-induced diaphragmatic hernia.

Takayasu H, Sato H, Sugimoto K, Puri P.

J Pediatr Surg. 2008 Feb;43(2):362-6. doi: 10.1016/j.jpedsurg.2007.10.047.

PMID:
18280291
12.

A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect.

Lin X, Huo Z, Liu X, Zhang Y, Li L, Zhao H, Yan B, Liu Y, Yang Y, Chen YH.

J Hum Genet. 2010 Oct;55(10):662-7. doi: 10.1038/jhg.2010.84. Epub 2010 Jul 15.

PMID:
20631719
13.

A case of pancreatic agenesis and congenital heart defects with a novel GATA6 nonsense mutation: evidence of haploinsufficiency due to nonsense-mediated mRNA decay.

Suzuki S, Nakao A, Sarhat AR, Furuya A, Matsuo K, Tanahashi Y, Kajino H, Azuma H.

Am J Med Genet A. 2014 Feb;164A(2):476-9. doi: 10.1002/ajmg.a.36275. Epub 2013 Dec 5.

PMID:
24310933
14.

Novel NKX2-5 mutations responsible for congenital heart disease.

Wang J, Liu XY, Yang YQ.

Genet Mol Res. 2011 Nov 29;10(4):2905-15. doi: 10.4238/2011.November.29.1.

15.

Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic hernia.

Yu L, Bennett JT, Wynn J, Carvill GL, Cheung YH, Shen Y, Mychaliska GB, Azarow KS, Crombleholme TM, Chung DH, Potoka D, Warner BW, Bucher B, Lim FY, Pietsch J, Stolar C, Aspelund G, Arkovitz MS; University of Washington Center for Mendelian Genomics, Mefford H, Chung WK.

J Med Genet. 2014 Mar;51(3):197-202. doi: 10.1136/jmedgenet-2013-101989. Epub 2014 Jan 2.

16.

GATA transcription factors in congenital heart defects: a commentary on a novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect.

Kodo K, Yamagishi H.

J Hum Genet. 2010 Oct;55(10):637-8. doi: 10.1038/jhg.2010.105. Epub 2010 Aug 26. No abstract available.

PMID:
20739941
17.

Human gene copy number spectra analysis in congenital heart malformations.

Tomita-Mitchell A, Mahnke DK, Struble CA, Tuffnell ME, Stamm KD, Hidestrand M, Harris SE, Goetsch MA, Simpson PM, Bick DP, Broeckel U, Pelech AN, Tweddell JS, Mitchell ME.

Physiol Genomics. 2012 May 1;44(9):518-41. doi: 10.1152/physiolgenomics.00013.2012. Epub 2012 Feb 7.

18.

Novel GATA6 loss-of-function mutation responsible for familial atrial fibrillation.

Li J, Liu WD, Yang ZL, Yang YQ.

Int J Mol Med. 2012 Oct;30(4):783-90. doi: 10.3892/ijmm.2012.1068. Epub 2012 Jul 18.

PMID:
22824924
19.

GATA6 loss-of-function mutations contribute to familial dilated cardiomyopathy.

Xu L, Zhao L, Yuan F, Jiang WF, Liu H, Li RG, Xu YJ, Zhang M, Fang WY, Qu XK, Yang YQ, Qiu XB.

Int J Mol Med. 2014 Nov;34(5):1315-22. doi: 10.3892/ijmm.2014.1896. Epub 2014 Aug 13.

PMID:
25119427
20.

Zac1 is an essential transcription factor for cardiac morphogenesis.

Yuasa S, Onizuka T, Shimoji K, Ohno Y, Kageyama T, Yoon SH, Egashira T, Seki T, Hashimoto H, Nishiyama T, Kaneda R, Murata M, Hattori F, Makino S, Sano M, Ogawa S, Prall OW, Harvey RP, Fukuda K.

Circ Res. 2010 Apr 2;106(6):1083-91. doi: 10.1161/CIRCRESAHA.109.214130. Epub 2010 Feb 18.

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