Ichthyosis vulgaris (IV), characterized by mild scaling on limbs and lower abdomen, has an incidence of 1 in 250. Smith, McLean, and colleagues demonstrate that common mutations in filaggrin underlie IV. Filaggrin aggregates keratin intermediate filaments and is cross-linked into the cornified envelope to form the epidermal barrier. These findings reinforce the importance of the epidermal barrier in pathogenesis of skin diseases
Ichthyosis vulgaris (IV; OMIM # 146700) is the most common inherited disorders of keratinization and...
Ichthyosis vulgaris (OMIM 146700) is the most common inherited disorder of keratinization and one of...
Epidermolytic hyperkeratosis is an autosomal dominant ichthyosis characterized by blistering, especi...
Ichthyosis vulgaris (IV), characterized by mild scaling on limbs and lower abdomen, has an incidence...
We have recently shown that loss-of-function mutations in the filaggrin gene, carried by about 10% o...
Prevalent mutations in the FLG gene underlie the common skin disorder ichthyosis vulgaris and are si...
The main proteinaceous component of the keratohyalin granules within the granular layer keratinocyte...
The discovery, in 2006, that loss-of-function mutations in the filaggrin (FLG) gene are the cause of...
Although mutations in the filaggrin gene (FLG) have been shown to be associated with ichthyosis vulg...
One of the most important roles of the skin is the formation of an effective barrier to prevent desi...
Atopic dermatitis (AD) is a common, complex inflammatory skin disorder where a defect skin barrier i...
Filaggrin is an abundant protein of the outer epidermis that is essential for terminal differentiati...
Although it is widely accepted that filaggrin (FLG) deficiency contributes to an abnormal barrier fu...
Mutations inactivating the STS gene cause X-linked ichthyosis (XLI), whereas null mutations in the F...
Ichthyosis vulgaris (IV; OMIM # 146700) is the most common inherited disorders of keratinization and...
Ichthyosis vulgaris (OMIM 146700) is the most common inherited disorder of keratinization and one of...
Epidermolytic hyperkeratosis is an autosomal dominant ichthyosis characterized by blistering, especi...
Ichthyosis vulgaris (IV), characterized by mild scaling on limbs and lower abdomen, has an incidence...
We have recently shown that loss-of-function mutations in the filaggrin gene, carried by about 10% o...
Prevalent mutations in the FLG gene underlie the common skin disorder ichthyosis vulgaris and are si...
The main proteinaceous component of the keratohyalin granules within the granular layer keratinocyte...
The discovery, in 2006, that loss-of-function mutations in the filaggrin (FLG) gene are the cause of...
Although mutations in the filaggrin gene (FLG) have been shown to be associated with ichthyosis vulg...
One of the most important roles of the skin is the formation of an effective barrier to prevent desi...
Atopic dermatitis (AD) is a common, complex inflammatory skin disorder where a defect skin barrier i...
Filaggrin is an abundant protein of the outer epidermis that is essential for terminal differentiati...
Although it is widely accepted that filaggrin (FLG) deficiency contributes to an abnormal barrier fu...
Mutations inactivating the STS gene cause X-linked ichthyosis (XLI), whereas null mutations in the F...
Ichthyosis vulgaris (IV; OMIM # 146700) is the most common inherited disorders of keratinization and...
Ichthyosis vulgaris (OMIM 146700) is the most common inherited disorder of keratinization and one of...
Epidermolytic hyperkeratosis is an autosomal dominant ichthyosis characterized by blistering, especi...