- Home
- Publications
- Publication Search
- Publication Details
Title
Desmosomal genodermatoses
Authors
Keywords
-
Journal
BRITISH JOURNAL OF DERMATOLOGY
Volume 166, Issue 1, Pages 36-45
Publisher
Wiley
Online
2011-09-20
DOI
10.1111/j.1365-2133.2011.10640.x
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Cardiomyopathy with alopecia and palmoplantar keratoderma (CAPK) is caused by a JUP mutation
- (2011) H. Erken et al. BRITISH JOURNAL OF DERMATOLOGY
- A case of monilethrix caused by novel compound heterozygous mutations in the desmoglein 4 (DSG4) gene
- (2011) M. Farooq et al. BRITISH JOURNAL OF DERMATOLOGY
- Recent progress in the genetics of cardiomyopathy and its role in the clinical evaluation of patients with cardiomyopathy
- (2011) Nina Ghosh et al. CURRENT OPINION IN CARDIOLOGY
- Lack of plakoglobin leads to lethal congenital epidermolysis bullosa: a novel clinico-genetic entity
- (2011) Manuela Pigors et al. HUMAN MOLECULAR GENETICS
- Deconstructing the skin: cytoarchitectural determinants of epidermal morphogenesis
- (2011) Cory L. Simpson et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- The three-dimensional molecular structure of the desmosomal plaque
- (2011) A. Al-Amoudi et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- No Evidence of Skin Blisters with Human Desmocollin-3 Gene Mutation
- (2010) Aimee S. Payne AMERICAN JOURNAL OF HUMAN GENETICS
- Loss of Corneodesmosin Leads to Severe Skin Barrier Defect, Pruritus, and Atopy: Unraveling the Peeling Skin Disease
- (2010) Vinzenz Oji et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Desmosomes: adhesive strength and signalling in health and disease
- (2010) Helen A. Thomason et al. BIOCHEMICAL JOURNAL
- Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice
- (2010) Veronique Fressart et al. EUROPACE
- 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
- Inflammatory Peeling Skin Syndrome Caused by a Mutation in CDSN Encoding Corneodesmosin
- (2010) Shirli Israeli et al. JOURNAL OF INVESTIGATIVE DERMATOLOGY
- Pervanadate stabilizes desmosomes
- (2010) David R. Garrod et al. Cell Adhesion & Migration
- A Homozygous Nonsense Mutation in the Human Desmocollin-3 (DSC3) Gene Underlies Hereditary Hypotrichosis and Recurrent Skin Vesicles
- (2009) Muhammad Ayub et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Mutation inDSG1causing autosomal dominant striate palmoplantar keratoderma
- (2009) M. Zamiri et al. BRITISH JOURNAL OF DERMATOLOGY
- Lethal Acantholytic Epidermolysis Bullosa
- (2009) John A. McGrath et al. DERMATOLOGIC CLINICS
- Ectodermal Dysplasia-Skin Fragility Syndrome
- (2009) John A. McGrath et al. DERMATOLOGIC CLINICS
- Skin and heart: une liaison dangereuse
- (2009) Maria C. Bolling et al. EXPERIMENTAL DERMATOLOGY
- Desmocollin 3-mediated Binding Is Crucial for Keratinocyte Cohesion and Is Impaired in Pemphigus
- (2009) Volker Spindler et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- 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
- Compound Heterozygous Desmoplakin Mutations Result in a Phenotype with a Combination of Myocardial, Skin, Hair, and Enamel Abnormalities
- (2009) My G. Mahoney et al. JOURNAL OF INVESTIGATIVE DERMATOLOGY
- The Desmosome
- (2009) E. Delva et al. Cold Spring Harbor Perspectives in Biology
- Structural studies on desmosomes
- (2008) Ashraf Al-Amoudi et al. BIOCHEMICAL SOCIETY TRANSACTIONS
- Homozygous Mutation of Desmocollin-2 in Arrhythmogenic Right Ventricular Cardiomyopathy with Mild Palmoplantar Keratoderma and Woolly Hair
- (2008) M.A. Simpson et al. CARDIOLOGY
- Novel mutations inDSG1causing striate palmoplantar keratoderma
- (2008) D. Hershkovitz et al. CLINICAL AND EXPERIMENTAL DERMATOLOGY
- Loss of desmocollin 3 in mice leads to epidermal blistering
- (2008) J. Chen et al. JOURNAL OF CELL SCIENCE
- The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB
- (2008) Jo-David Fine et al. JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY
- G protein–coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth
- (2008) Sandra M Pasternack et al. NATURE GENETICS
- Targeted deletion of the murine corneodesmosin gene delineates its essential role in skin and hair physiology
- (2008) M. Matsumoto et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Desmosome structure, composition and function
- (2007) David Garrod et al. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationPublish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn More