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Filaggrin (FLG) is a key structural protein expressed in epidermal keratinocytes. Mutations in the filaggrin gene (FLG) are strongly linked to atopic dermatitis (AD) and allergic inflammation occurring later in life at distant body locations in AD patients. Keratinocytes secrete exosomes, small, lip...
ORGANISM(S): Homo sapiens (Human) 
2022-08-12 | PXD026859 | Pride
Gene expression profiling of filaggrin-insufficient keratinocytes exposed to inflammatory mediators and allergens
Loss-of-function mutations in the filaggrin gene are heavily associated with the incidence and severity of atopic dermatitis. Moreover, filaggrin insufficiency in epidermal keratinocytes can lead to persistent allergic inflammation and an associated immune response suggesting a role for this protein...
ORGANISM(S): Homo sapiens 
2022-05-20 | GSE203409 | GEO
Atopic eczema is an itchy inflammatory disorder characterised by skin barrier dysfunction. Loss-of-function mutations in the gene encoding filaggrin (FLG) are a major risk factor, but the mechanisms by which filaggrin haploinsufficiency leads to atopic inflammation remain incompletely understood. Sk...
ORGANISM(S): Homo sapiens (Human) 
2019-08-14 | PXD014875 | Pride
Scleritis is a severe inflammatory ocular disorder with unknown pathogenesis. Using a mass spectrometry approach, we investigated healthy sclera and sclera affected by non-infectious scleritis for differentially expressed proteins. Therefore, we collected scleral samples of enucleated eyes due to se...
ORGANISM(S): Homo sapiens (Human) 
2023-05-10 | PXD038727 | Pride
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