Loss of desmoglein 1 associated with palmoplantar keratoderma, dermatitis and multiple allergies

Atopic dermatitis: Scratching through the complexity of barrier dysfunction

(2013) Eli Sprecher et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Desmoglein-1, differentiation, and disease

(2013) Christoph M. Hammers et al.   JOURNAL OF CLINICAL INVESTIGATION

Desmoglein-1/Erbin interaction suppresses ERK activation to support epidermal differentiation

(2013) Robert M. Harmon et al.   JOURNAL OF CLINICAL INVESTIGATION

Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting

(2013) Liat Samuelov et al.   NATURE GENETICS

Epidermal barrier dysfunction and cutaneous sensitization in atopic diseases

(2012) Akiharu Kubo et al.   JOURNAL OF CLINICAL INVESTIGATION

Lack of plakoglobin leads to lethal congenital epidermolysis bullosa: a novel clinico-genetic entity

(2011) Manuela Pigors et al.   HUMAN MOLECULAR GENETICS

Mutation inDSG1causing autosomal dominant striate palmoplantar keratoderma

(2009) M. Zamiri et al.   BRITISH JOURNAL OF DERMATOLOGY

Desmoglein 1–dependent suppression of EGFR signaling promotes epidermal differentiation and morphogenesis

(2009) Spiro Getsios et al.   JOURNAL OF CELL BIOLOGY

Mutations in the desmoglein 1 gene in five Pakistani families with striate palmoplantar keratoderma

(2009) Martha B. Dua-Awereh et al.   JOURNAL OF DERMATOLOGICAL SCIENCE

Disadhesion of epidermal keratinocytes: A histologic clue to palmoplantar keratodermas caused by DSG1 mutations

(2009) Reuven Bergman et al.   JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY

Novel mutations inDSG1causing striate palmoplantar keratoderma

(2008) D. Hershkovitz et al.   CLINICAL AND EXPERIMENTAL DERMATOLOGY