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Items: 1 to 20 of 100

1.

Novel missense variants of ZFPM2/FOG2 identified in conotruncal heart defect patients do not impair interaction with GATA4.

Zhang W, Shen L, Deng Z, Ding Y, Mo X, Xu Z, Gao Q, Yi L.

PLoS One. 2014 Jul 15;9(7):e102379. doi: 10.1371/journal.pone.0102379. eCollection 2014.

2.

New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle.

De Luca A, Sarkozy A, Ferese R, Consoli F, Lepri F, Dentici ML, Vergara P, De Zorzi A, Versacci P, Digilio MC, Marino B, Dallapiccola B.

Clin Genet. 2011 Aug;80(2):184-90. doi: 10.1111/j.1399-0004.2010.01523.x. Epub 2010 Aug 2.

PMID:
20807224
3.

Identification of novel significant variants of ZFPM2/FOG2 in non-syndromic Tetralogy of Fallot and double outlet right ventricle in a Chinese Han population.

Huang X, Niu W, Zhang Z, Zhou C, Xu Z, Liu J, Su Z, Ding W, Zhang H.

Mol Biol Rep. 2014;41(4):2671-7. doi: 10.1007/s11033-014-3126-5. Epub 2014 Jan 28.

PMID:
24469719
4.

Novel ZFPM2/FOG2 variants in patients with double outlet right ventricle.

Tan ZP, Huang C, Xu ZB, Yang JF, Yang YF.

Clin Genet. 2012 Nov;82(5):466-71. doi: 10.1111/j.1399-0004.2011.01787.x. Epub 2011 Oct 30.

PMID:
21919901
5.

Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot.

Pizzuti A, Sarkozy A, Newton AL, Conti E, Flex E, Digilio MC, Amati F, Gianni D, Tandoi C, Marino B, Crossley M, Dallapiccola B.

Hum Mutat. 2003 Nov;22(5):372-7.

PMID:
14517948
6.

Mutations in the FOG2/ZFPM2 gene are associated with anomalies of human testis determination.

Bashamboo A, Brauner R, Bignon-Topalovic J, Lortat-Jacob S, Karageorgou V, Lourenco D, Guffanti A, McElreavey K.

Hum Mol Genet. 2014 Jul 15;23(14):3657-65. doi: 10.1093/hmg/ddu074. Epub 2014 Feb 18.

7.

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
8.

GATA4 sequence variants in patients with congenital heart disease.

Tomita-Mitchell A, Maslen CL, Morris CD, Garg V, Goldmuntz E.

J Med Genet. 2007 Dec;44(12):779-83.

9.

The regulation of Sox9 gene expression by the GATA4/FOG2 transcriptional complex in dominant XX sex reversal mouse models.

Manuylov NL, Fujiwara Y, Adameyko II, Poulat F, Tevosian SG.

Dev Biol. 2007 Jul 15;307(2):356-67. Epub 2007 May 3.

10.

Cardiac expression of Tnnt1 requires the GATA4-FOG2 transcription complex.

Manuylov NL, Tevosian SG.

ScientificWorldJournal. 2009 Jul 4;9:575-87. doi: 10.1100/tsw.2009.75.

11.

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5.

Garg V, Kathiriya IS, Barnes R, Schluterman MK, King IN, Butler CA, Rothrock CR, Eapen RS, Hirayama-Yamada K, Joo K, Matsuoka R, Cohen JC, Srivastava D.

Nature. 2003 Jul 24;424(6947):443-7. Epub 2003 Jul 6.

PMID:
12845333
12.

Proper coronary vascular development and heart morphogenesis depend on interaction of GATA-4 with FOG cofactors.

Crispino JD, Lodish MB, Thurberg BL, Litovsky SH, Collins T, Molkentin JD, Orkin SH.

Genes Dev. 2001 Apr 1;15(7):839-44.

13.

GATA4 loss-of-function mutations underlie familial tetralogy of fallot.

Yang YQ, Gharibeh L, Li RG, Xin YF, Wang J, Liu ZM, Qiu XB, Xu YJ, Xu L, Qu XK, Liu X, Fang WY, Huang RT, Xue S, Nemer G.

Hum Mutat. 2013 Dec;34(12):1662-71. doi: 10.1002/humu.22434. Epub 2013 Sep 17.

PMID:
24000169
14.

Gata4 is necessary for normal pulmonary lobar development.

Ackerman KG, Wang J, Luo L, Fujiwara Y, Orkin SH, Beier DR.

Am J Respir Cell Mol Biol. 2007 Apr;36(4):391-7. Epub 2006 Dec 1.

15.

Ovarian development in mice requires the GATA4-FOG2 transcription complex.

Manuylov NL, Smagulova FO, Leach L, Tevosian SG.

Development. 2008 Nov;135(22):3731-43. doi: 10.1242/dev.024653. Epub 2008 Oct 16.

16.

Identification of TBX5 mutations in a series of 94 patients with Tetralogy of Fallot.

Baban A, Postma AV, Marini M, Trocchio G, Santilli A, Pelegrini M, Sirleto P, Lerone M, Albanese SB, Barnett P, Boogerd CJ, Dallapiccola B, Digilio MC, Ravazzolo R, Pongiglione G.

Am J Med Genet A. 2014 Dec;164A(12):3100-7. doi: 10.1002/ajmg.a.36783. Epub 2014 Sep 26.

PMID:
25263169
17.

Correct dosage of Fog2 and Gata4 transcription factors is critical for fetal testis development in mice.

Bouma GJ, Washburn LL, Albrecht KH, Eicher EM.

Proc Natl Acad Sci U S A. 2007 Sep 18;104(38):14994-9. Epub 2007 Sep 11.

18.

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
19.

The phenotypic spectrum of ZIC3 mutations includes isolated d-transposition of the great arteries and double outlet right ventricle.

D'Alessandro LC, Latney BC, Paluru PC, Goldmuntz E.

Am J Med Genet A. 2013 Apr;161A(4):792-802. doi: 10.1002/ajmg.a.35849. Epub 2013 Feb 20.

20.

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.

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