Search
for
Sort by
Research 30 of 565
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Dysfunction of keratinocyte adhesion
- 875 A novel animal model of Desmoglein 1 (Dsg1) deficiency reveals an essential role for Dsg1 in epidermal barrier formation
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- LB1076 Using the frog embryonic epidermis as a model to study desmosome function during development
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Regulation of Hair Shedding by the Type 3 IP3 Receptor
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- A desmosomal cadherin controls multipotent hair follicle stem cell quiescence and orchestrates regeneration through adhesion signaling
- Biology and Genetics of Hair
- Stratum corneum dysfunction in dandruff
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Cutaneous Markers of Disorders Affecting Adult Horses
- Nanoparticles for Topical Application in the Treatment of Skin Dysfunctions—An Overview of Dermo-Cosmetic and Dermatological Products
- Hidradenitis suppurativa: A folliculotropic disease of innate immune barrier dysfunction?
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- Granzyme B in Autoimmune Skin Disease
- Understanding the Intricate Pathophysiology of Psoriasis and Related Skin Disorders
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- LB1081 Three-dimensional imaging of tight junction-network across multiple layers of human epidermis by array tomography using backscattered electron-mode scanning electron microscopy
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- 1314 Advanced age impairs self-renewal and biases fate choice of hair follicle dermal stem cells
- Store-operated calcium channels in skin
- Corneodesmosomes and corneodesmosin: from the stratum corneum cohesion to the pathophysiology of genodermatoses
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- Minimizing Skin Scarring through Biomaterial Design
- Wound healing: cellular mechanisms and pathological outcomes
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- 14-3-3σ Is Required for Club Hair Retention