ABCA12 Maintains the Epidermal Lipid Permeability Barrier by Facilitating Formation of Ceramide Linoleic Esters

Harlequin ichthyosis is a congenital scaling syndrome of the skin in which affected infants have epidermal hyperkeratosis and a defective permeability barrier. Mutations in the gene encoding a member of the ABCA transporter family, ABCA12, have been linked to harlequin ichthyosis, but the molecular...

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Autors principals: Zuo, Ying, Zhuang, Debbie Z., Han, Rong, Isaac, Giorgis, Tobin, Jennifer J., McKee, Mary, Welti, Ruth, Brissette, Janice L., Fitzgerald, Michael L., Freeman, Mason W.
Format: Artigo
Idioma:Inglês
Publicat: American Society for Biochemistry and Molecular Biology 2008
Matèries:
Lipids and Lipoproteins: Metabolism, Regulation, and Signaling
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2605993/
https://ncbi.nlm.nih.gov/pubmed/18957418
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M807377200
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