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Journal Abstract Search


242 related items for PubMed ID: 24665072

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  • 23. Mutant p63 causes defective expansion of ectodermal progenitor cells and impaired FGF signalling in AEC syndrome.
    Ferone G, Thomason HA, Antonini D, De Rosa L, Hu B, Gemei M, Zhou H, Ambrosio R, Rice DP, Acampora D, van Bokhoven H, Del Vecchio L, Koster MI, Tadini G, Spencer-Dene B, Dixon M, Dixon J, Missero C.
    EMBO Mol Med; 2012 Mar; 4(3):192-205. PubMed ID: 22247000
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  • 25. Growth, nutritional, and gastrointestinal aspects of ankyloblepharon-ectodermal defect-cleft lip and/or palate (AEC) syndrome.
    Motil KJ, Fete TJ.
    Am J Med Genet A; 2009 Sep; 149A(9):1922-5. PubMed ID: 19676058
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  • 26. Pathologic changes of skin and hair in ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome.
    Dishop MK, Bree AF, Hicks MJ.
    Am J Med Genet A; 2009 Sep; 149A(9):1935-41. PubMed ID: 19697429
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  • 29. Syndrome in question. Hay-Wells syndrome.
    Tonolli VM, Stolf HO, Tonello CS, Pires RB, Abbade LP.
    An Bras Dermatol; 2014 Sep; 89(2):363-4. PubMed ID: 24770526
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  • 34. Allele-specific silencing of EEC p63 mutant R304W restores p63 transcriptional activity.
    Novelli F, Lena AM, Panatta E, Nasser W, Shalom-Feuerstein R, Candi E, Melino G.
    Cell Death Dis; 2016 May 19; 7(5):e2227. PubMed ID: 27195674
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