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Journal Abstract Search

269 related items for PubMed ID: 16081467

  • 1. The establishment of a predictive mutational model of the forkhead domain through the analyses of FOXC2 missense mutations identified in patients with hereditary lymphedema with distichiasis.
    Berry FB, Tamimi Y, Carle MV, Lehmann OJ, Walter MA.
    Hum Mol Genet; 2005 Sep 15; 14(18):2619-27. PubMed ID: 16081467
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  • 2. A novel missense mutation and two microrearrangements in the FOXC2 gene of three families with lymphedema-distichiasis syndrome.
    Fauret AL, Tuleja E, Jeunemaitre X, Vignes S.
    Lymphology; 2010 Mar 15; 43(1):14-8. PubMed ID: 20552815
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  • 3. Novel FOXC2 missense mutation identified in patient with lymphedema-distichiasis syndrome and review.
    Dellinger MT, Thome K, Bernas MJ, Erickson RP, Witte MH.
    Lymphology; 2008 Sep 15; 41(3):98-102. PubMed ID: 19013876
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  • 5. Lymphedema-distichiasis syndrome: a distinct type of primary lymphedema caused by mutations in the FOXC2 gene.
    Vreeburg M, Heitink MV, Damstra RJ, Moog U, van Geel M, van Steensel MA.
    Int J Dermatol; 2008 Nov 15; 47 Suppl 1():52-5. PubMed ID: 18986489
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  • 7. Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivation.
    Beysen D, Moumné L, Veitia R, Peters H, Leroy BP, De Paepe A, De Baere E.
    Hum Mol Genet; 2008 Jul 01; 17(13):2030-8. PubMed ID: 18372316
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  • 8. Lymphedema-distichiasis syndrome without FOXC2 mutation: evidence for chromosome 16 duplication upstream of FOXC2.
    Witte MH, Erickson RP, Khalil M, Dellinger M, Bernas M, Grogan T, Nitta H, Feng J, Duggan D, Witte CL.
    Lymphology; 2009 Dec 01; 42(4):152-60. PubMed ID: 20218083
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  • 14. Novel FOXC2 Mutation in Hereditary Distichiasis Impairs DNA-Binding Activity and Transcriptional Activation.
    Zhang L, He J, Han B, Lu L, Fan J, Zhang H, Ge S, Zhou Y, Jia R, Fan X.
    Int J Biol Sci; 2016 Dec 01; 12(9):1114-20. PubMed ID: 27570485
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  • 18. A case of lymphedema-distichiasis syndrome carrying a new de novo frameshift FOXC2 mutation.
    Fabretto A, Shardlow A, Faletra F, Lepore L, Hladnik U, Gasparini P.
    Ophthalmic Genet; 2010 Jun 01; 31(2):98-100. PubMed ID: 20450314
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  • 20. Comparative lymphatic, ocular, and metabolic phenotypes of Foxc2 haploinsufficient and aP2-FOXC2 transgenic mice.
    Noon A, Hunter RJ, Witte MH, Kriederman B, Bernas M, Rennels M, Percy D, Enerbäck S, Erickson RP.
    Lymphology; 2006 Jun 01; 39(2):84-94. PubMed ID: 16910099
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