Mutations in the gene-encoding filaggrin (FLG), a key molecule involved in skin barrier function, have been shown to be a major predisposing factor for atopic dermatitis (AD; eczema). To elucidate the pathomechanisms underlying filaggrin-related AD, we investigated stratum corneum (SC) hydration and transepidermal water loss (TEWL) as parameters of barrier function in AD patients harboring FLG mutations compared to AD patients without any FLG mutation. In filaggrin-related AD, SC hydration was both significantly reduced (P<0.01–0.05) and thicker (P<0.01–0.05) than that in healthy controls. TEWL was demonstrably increased in non-filaggrin AD compared to healthy controls (P<0.01–0.05). The objective score of atopic dermatitis (OSCORAD), a dis...
Atopic dermatitis, AD (synonym eczema) is a chronic inflammatory skin disease. It affects between 1...
Background Loss-of-function mutations in the skin barrier gene filaggrin (FLG) increase the risk of...
The discovery, in 2006, that loss-of-function mutations in the filaggrin (FLG) gene are the cause of...
Mutations in the gene-encoding filaggrin (FLG), a key molecule involved in skin barrier function, ha...
Mutations in the gene-encoding filaggrin (FLG), a key molecule involved in skin barrier function, ha...
ABSTRACTFilaggrin is a key protein that facilitates terminal differentiation of the epidermis and fo...
BACKGROUND Filaggrin (FLG) deficiency is a well-known predisposing factor for the development of ...
We have recently shown that loss-of-function mutations in the filaggrin gene, carried by about 10% o...
Recent genetic findings demonstrate an important role for the epidermal protein filaggrin in the aet...
The recent identification of loss-of-function mutations in the structural protein filaggrin as a wid...
Atopic dermatitis (AD) is a common, complex inflammatory skin disorder where a defect skin barrier i...
The recent identification of loss-of-function mutations in the structural protein filaggrin as a wid...
Atopic dermatitis (AD) results from strong genetic and environmental interactions. AD shows genetic ...
Atopic dermatitis, AD (synonym eczema) is a chronic inflammatory skin disease. It affects between 1...
Background Loss-of-function mutations in the skin barrier gene filaggrin (FLG) increase the risk of...
The discovery, in 2006, that loss-of-function mutations in the filaggrin (FLG) gene are the cause of...
Mutations in the gene-encoding filaggrin (FLG), a key molecule involved in skin barrier function, ha...
Mutations in the gene-encoding filaggrin (FLG), a key molecule involved in skin barrier function, ha...
ABSTRACTFilaggrin is a key protein that facilitates terminal differentiation of the epidermis and fo...
BACKGROUND Filaggrin (FLG) deficiency is a well-known predisposing factor for the development of ...
We have recently shown that loss-of-function mutations in the filaggrin gene, carried by about 10% o...
Recent genetic findings demonstrate an important role for the epidermal protein filaggrin in the aet...
The recent identification of loss-of-function mutations in the structural protein filaggrin as a wid...
Atopic dermatitis (AD) is a common, complex inflammatory skin disorder where a defect skin barrier i...
The recent identification of loss-of-function mutations in the structural protein filaggrin as a wid...
Atopic dermatitis (AD) results from strong genetic and environmental interactions. AD shows genetic ...
Atopic dermatitis, AD (synonym eczema) is a chronic inflammatory skin disease. It affects between 1...
Background Loss-of-function mutations in the skin barrier gene filaggrin (FLG) increase the risk of...
The discovery, in 2006, that loss-of-function mutations in the filaggrin (FLG) gene are the cause of...