We have recently shown that loss-of-function mutations in the filaggrin gene, carried by about 10% of people of European ethnicity, cause ichthyosis vulgaris and are strong predisposing factors for atopic dermatitis and asthma secondary to atopic dermatitis. These results demonstrate a prominent role for the epidermal barrier in atopic disease and have important implications for the study of complex traits
Mutations in the gene-encoding filaggrin (FLG), a key molecule involved in skin barrier function, ha...
The recent identification of loss-of-function mutations in the structural protein filaggrin as a wid...
The discovery that null mutations in the filaggrin gene (FLG) are associated with atopic eczema repr...
Prevalent mutations in the FLG gene underlie the common skin disorder ichthyosis vulgaris and are si...
ABSTRACTFilaggrin is a key protein that facilitates terminal differentiation of the epidermis and fo...
Atopic dermatitis (AD) results from strong genetic and environmental interactions. AD shows genetic ...
Background: Atopic dermatitis (AD) is a chronic inflammatory skin disease with a strong genetic back...
BACKGROUND: Atopic dermatitis (AD) is a chronic inflammatory skin disease with a strong genetic ...
The discovery, in 2006, that loss-of-function mutations in the filaggrin (FLG) gene are the cause of...
Ichthyosis vulgaris (IV; OMIM # 146700) is the most common inherited disorders of keratinization and...
Recent genetic findings demonstrate an important role for the epidermal protein filaggrin in the aet...
Atopic dermatitis (AD) is a common, complex inflammatory skin disorder where a defect skin barrier i...
Ichthyosis vulgaris (IV), characterized by mild scaling on limbs and lower abdomen, has an incidence...
There is an increasing number of experimental, genetic and clinical evidence of atopic dermatitis ex...
BACKGROUND: Several common genetic and environmental disease mechanisms are important for the pathop...
Mutations in the gene-encoding filaggrin (FLG), a key molecule involved in skin barrier function, ha...
The recent identification of loss-of-function mutations in the structural protein filaggrin as a wid...
The discovery that null mutations in the filaggrin gene (FLG) are associated with atopic eczema repr...
Prevalent mutations in the FLG gene underlie the common skin disorder ichthyosis vulgaris and are si...
ABSTRACTFilaggrin is a key protein that facilitates terminal differentiation of the epidermis and fo...
Atopic dermatitis (AD) results from strong genetic and environmental interactions. AD shows genetic ...
Background: Atopic dermatitis (AD) is a chronic inflammatory skin disease with a strong genetic back...
BACKGROUND: Atopic dermatitis (AD) is a chronic inflammatory skin disease with a strong genetic ...
The discovery, in 2006, that loss-of-function mutations in the filaggrin (FLG) gene are the cause of...
Ichthyosis vulgaris (IV; OMIM # 146700) is the most common inherited disorders of keratinization and...
Recent genetic findings demonstrate an important role for the epidermal protein filaggrin in the aet...
Atopic dermatitis (AD) is a common, complex inflammatory skin disorder where a defect skin barrier i...
Ichthyosis vulgaris (IV), characterized by mild scaling on limbs and lower abdomen, has an incidence...
There is an increasing number of experimental, genetic and clinical evidence of atopic dermatitis ex...
BACKGROUND: Several common genetic and environmental disease mechanisms are important for the pathop...
Mutations in the gene-encoding filaggrin (FLG), a key molecule involved in skin barrier function, ha...
The recent identification of loss-of-function mutations in the structural protein filaggrin as a wid...
The discovery that null mutations in the filaggrin gene (FLG) are associated with atopic eczema repr...