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Items: 1 to 20 of 66

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.

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
4.

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
5.

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
6.

Identification of ZFPM2 mutations in sporadic conotruncal heart defect patients.

Pu T, Liu Y, Xu R, Li F, Chen S, Sun K.

Mol Genet Genomics. 2018 Feb;293(1):217-223. doi: 10.1007/s00438-017-1373-6. Epub 2017 Oct 10.

PMID:
29018978
7.

Mutation Screening of Gata4 Gene in CTD Patients Within Chinese Han Population.

Liu Y, Li B, Xu Y, Sun K.

Pediatr Cardiol. 2017 Mar;38(3):506-512. doi: 10.1007/s00246-016-1542-0. Epub 2017 Feb 4.

PMID:
28161810
8.

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.

PMID:
24549039
9.

Multiple gene variations contributed to congenital heart disease via GATA family transcriptional regulation.

Qian Y, Xiao D, Guo X, Chen H, Hao L, Ma X, Huang G, Ma D, Wang H.

J Transl Med. 2017 Apr 3;15(1):69. doi: 10.1186/s12967-017-1173-0.

10.

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.

11.

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
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.

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.

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.

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.

17.

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.

18.

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.

19.

A novel mutation in the GATA4 gene in patients with Tetralogy of Fallot.

Nemer G, Fadlalah F, Usta J, Nemer M, Dbaibo G, Obeid M, Bitar F.

Hum Mutat. 2006 Mar;27(3):293-4.

PMID:
16470721
20.

Candidate genes for congenital diaphragmatic hernia from animal models: sequencing of FOG2 and PDGFRalpha reveals rare variants in diaphragmatic hernia patients.

Bleyl SB, Moshrefi A, Shaw GM, Saijoh Y, Schoenwolf GC, Pennacchio LA, Slavotinek AM.

Eur J Hum Genet. 2007 Sep;15(9):950-8. Epub 2007 Jun 13.

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