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Journal Abstract Search

144 related items for PubMed ID: 25025186

  • 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; 9(7):e102379. PubMed ID: 25025186
    [Abstract] [Full Text] [Related]

  • 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. PubMed ID: 20807224
    [Abstract] [Full Text] [Related]

  • 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 Aug; 41(4):2671-7. PubMed ID: 24469719
    [Abstract] [Full Text] [Related]

  • 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. PubMed ID: 21919901
    [Abstract] [Full Text] [Related]

  • 5. 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. PubMed ID: 29018978
    [Abstract] [Full Text] [Related]

  • 6. 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. PubMed ID: 14517948
    [Abstract] [Full Text] [Related]

  • 7. Analysis of variants in GATA4 and FOG2/ZFPM2 demonstrates benign contribution to 46,XY disorders of sex development.
    van den Bergen JA, Robevska G, Eggers S, Riedl S, Grover SR, Bergman PB, Kimber C, Jiwane A, Khan S, Krausz C, Raza J, Atta I, Davis SR, Ono M, Harley V, Faradz SMH, Sinclair AH, Ayers KL.
    Mol Genet Genomic Med; 2020 Mar; 8(3):e1095. PubMed ID: 31962012
    [Abstract] [Full Text] [Related]

  • 8. 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. PubMed ID: 28161810
    [Abstract] [Full Text] [Related]

  • 9. 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. PubMed ID: 24549039
    [Abstract] [Full Text] [Related]

  • 10. 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 03; 15(1):69. PubMed ID: 28372585
    [Abstract] [Full Text] [Related]

  • 11. A loss-of-function mutation p.T52S in RIPPLY3 is a potential predisposing genetic risk factor for Chinese Han conotruncal heart defect patients without the 22q11.2 deletion/duplication.
    Hong N, Zhang E, Wang Q, Zhang X, Li F, Fu Q, Xu R, Yu Y, Chen S, Xu Y, Sun K.
    J Transl Med; 2018 Sep 21; 16(1):260. PubMed ID: 30241482
    [Abstract] [Full Text] [Related]

  • 12. Functional analysis of rare variants of GATA4 identified in Chinese patients with congenital heart defect.
    Zhao Z, Zhan Y, Chen W, Ma X, Sheng W, Huang G.
    Genesis; 2019 Nov 21; 57(11-12):e23333. PubMed ID: 31513339
    [Abstract] [Full Text] [Related]

  • 13. 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 21; 44(12):779-83. PubMed ID: 18055909
    [Abstract] [Full Text] [Related]

  • 14. 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. PubMed ID: 17540364
    [Abstract] [Full Text] [Related]

  • 15. Cardiac expression of Tnnt1 requires the GATA4-FOG2 transcription complex.
    Manuylov NL, Tevosian SG.
    ScientificWorldJournal; 2009 Jul 04; 9():575-87. PubMed ID: 19578715
    [Abstract] [Full Text] [Related]

  • 16. Human Genetics of Tetralogy of Fallot and Double-Outlet Right Ventricle.
    Dorn C, Perrot A, Grunert M, Rickert-Sperling S.
    Adv Exp Med Biol; 2024 Jul 04; 1441():629-644. PubMed ID: 38884738
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  • 20. 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. PubMed ID: 17848526
    [Abstract] [Full Text] [Related]

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