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• W2899188813 endingPage "1171" @default.
• W2899188813 startingPage "1164" @default.
• W2899188813 abstract "Abstract 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 crosslinked by transglutaminase‐1 ( TG m‐1), or a yet unidentified enzyme, for normal skin barrier formation. We hypothesized that inactivating TGM 1 mutations will lead to a compensatory overexpression of the transcripts involved in skin barrier repair, including many other ARCI ‐causing genes. Using microarray, we examined the global mRNA expression profile in skin biopsies from five ARCI patients with TGM 1 mutations and four healthy controls. There were a total of 599 significantly differentially expressed genes (adjusted P < 0.05), out of which 272 showed more than 1.5 log2fold‐change ( FC ) up‐ or down‐regulation. Functional classification of the latter group of transcripts showed enrichment of mRNA encoding proteins mainly associated with biological pathways involved in keratinocyte differentiation and immune response. Moreover, the expression of seven out of twelve ARCI ‐causing genes was significantly increased ( FC = 0.98‐2.05). Also, many of the genes involved in keratinocyte differentiation (cornified envelope formation) and immune response (antimicrobial peptides and proinflammatory cytokines) were upregulated. The results from the microarray analysis were also verified for selected genes at the mRNA level by qPCR and at the protein level by semi‐quantitative immunofluorescence. The upregulation of these genes might reflect a compensatory induction of acylCer biosynthesis as a part of a global barrier repair response in the patient′s epidermis." @default.
• W2899188813 created "2018-11-09" @default.
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• W2899188813 date "2018-12-21" @default.
• W2899188813 modified "2023-09-26" @default.
• W2899188813 title "Patients with congenital ichthyosis and <i> <scp>TGM</scp> 1 </i> mutations overexpress other <scp>ARCI</scp> genes in the skin: Part of a barrier repair response?" @default.
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• W2899188813 doi "https://doi.org/10.1111/exd.13813" @default.
• W2899188813 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7379499" @default.
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• W2899188813 hasPublicationYear "2018" @default.
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