Patients with congenital ichthyosis and TGM1 mutations overexpress other ARCI genes in the skin: Part of a barrier repair response?

Autosomal recessive congenital ichthyosis (ARCI) is a group of monogenic skin disorders caused by mutations in any of at least 12 different genes, many of which are involved in the epidermal synthesis of ω‐O‐acylceramides (acylCer). AcylCer are essential precursors of the corneocyte lipid envelope c...

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Detalles Bibliográficos
Autores principales: Zhang, Hanqian, Ericsson, Maja, Weström, Simone, Vahlquist, Anders, Virtanen, Marie, Törmä, Hans
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Patterns of Expression
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379499/
https://www.ncbi.nlm.nih.gov/pubmed/30372788
http://dx.doi.org/10.1111/exd.13813

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379499/
https://www.ncbi.nlm.nih.gov/pubmed/30372788
http://dx.doi.org/10.1111/exd.13813

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