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

Lethal acantholytic epidermolysis bullosa due to a novel homozygous deletion in DSP: expanding the phenotype and implications for desmoplakin function in skin and heart

(2010) M.C. Bolling et al.   BRITISH JOURNAL OF DERMATOLOGY

Lower than expected desmosomal gene mutation prevalence in endurance athletes with complex ventricular arrhythmias of right ventricular origin

(2010) A. La Gerche et al.   HEART

Homozygous Mutations in the 5′ Region of the JUP Gene Result in Cutaneous Disease but Normal Heart Development in Children

(2010) Rita M. Cabral et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

Insights from a Desmoplakin Mutation Identified in Lethal Acantholytic Epidermolysis Bullosa

(2010) Ryan P. Hobbs et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

Kindlin-1 Is Required for RhoGTPase-Mediated Lamellipodia Formation in Keratinocytes

(2009) Cristina Has et al.   AMERICAN JOURNAL OF PATHOLOGY

Comprehensive Desmosome Mutation Analysis in North Americans With Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy

(2009) A. Dénise den Haan et al.   Circulation-Cardiovascular Genetics

Desmosomes at a glance

(2009) Bhushan V. Desai et al.   JOURNAL OF CELL SCIENCE

Plasmin Plays a Role in the In Vitro Generation of the Linear IgA Dermatosis Antigen LADB97

(2009) Silke C. Hofmann et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY