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Research 61–90 of 514
- Genetics of Inherited Ichthyoses and Related Diseases
- The role of oxidative damage in poor scalp health: ramifications to causality and associated hair growth
- Biologics in the management of childhood atopic dermatitis
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Skin, Genetic Defects, and Aging
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- Cell death by cornification
- Matriptase: Potent Proteolysis on the Cell Surface
- The regulation of skin homeostasis, repair and the pathogenesis of skin diseases by spatiotemporal activation of epidermal mTOR signaling
- Hair follicles modulate skin barrier function
- “Structural imprinting” of the cutaneous immune effector function
- The Fate of Epidermal Tight Junctions in the stratum corneum: Their Involvement in the Regulation of Desquamation and Phenotypic Expression of Certain Skin Conditions
- Systematic characterization of the barrier function of diverse ex vivo models of damaged human skin
- Transdermal delivery of mixnoxidil with block copolymer nanoparticles
- First Symposium of Ichthyosis Experts
- Transglutaminase-3 Enzyme: A Putative Actor in Human Hair Shaft Scaffolding?
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Redefining the Skin Barrier: A Microbiome‐Integrated Multilayered Defense Model
- Autophagy-Mediated Cellular Remodeling during Terminal Differentiation of Keratinocytes in the Epidermis and Skin Appendages
- Cultured Human Foreskin as a Model System for Evaluating Ionizing Radiation-Induced Skin Injury
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- A Multifaceted View on Ageing of the Hair and Scalp
- Regulation of Involucrin Gene Expression
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Proteomic analysis of hair shaft and nail plate.
- Epidermal PPARγ Is a Key Homeostatic Regulator of Cutaneous Inflammation and Barrier Function in Mouse Skin
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Proliferative and Non-Proliferative Lesions of the Rat and Mouse Integument
- Developing stratified epithelia: lessons from the epidermis and thymus