p63 control of desmosome gene expression and adhesion is compromised in AEC syndrome

Ankyloblepharon, ectodermal defects, cleft lip/palate (AEC) syndrome is a rare autosomal dominant disorder caused by mutations in the p63 gene, essential for embryonic development of stratified epithelia. The most severe cutaneous manifestation of this disorder is the long-lasting skin fragility ass...

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Main Authors: Ferone, Giustina, Mollo, Maria Rosaria, Thomason, Helen A., Antonini, Dario, Zhou, Huiqing, Ambrosio, Raffaele, De Rosa, Laura, Salvatore, Domenico, Getsios, Spiro, van Bokhoven, Hans, Dixon, Jill, Missero, Caterina
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2013
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3542863/
https://ncbi.nlm.nih.gov/pubmed/23108156
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/dds464
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