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Research 871–900 of 1000+
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Epidermal Development in Mammals: Key Regulators, Signals from Beneath, and Stem Cells
- Inducible deletion of epidermal <i>Dicer</i> and <i>Drosha</i> reveals multiple functions for miRNAs in postnatal skin
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- The molecular basis of human keratin disorders
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Epidermal growth factor delays the development of the epidermis and hair follicles of mice during growth of the first coat
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Requirement of zinc transporter ZIP10 for epidermal development: Implication of the ZIP10–p63 axis in epithelial homeostasis
- Functional Skin Grafts: Where Biomaterials Meet Stem Cells
- A Scarless Healing Tale: Comparing Homeostasis and Wound Healing of Oral Mucosa With Skin and Oesophagus
- Normal Fur Development and Sebum Production Depends on Fatty Acid 2-Hydroxylase Expression in Sebaceous Glands
- Integral hair lipid in human hair follicle
- Transglutaminase-3, an esophageal cancer-related gene
- Genes for Hair and Avian Keratins
- Transglutaminase-3 Enzyme: A Putative Actor in Human Hair Shaft Scaffolding?
- In situ labeling of DNA reveals interindividual variation in nuclear DNA breakdown in hair and may be useful to predict success of forensic genotyping of hair
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Inherited disorders of the skin in human and mouse: from development to differentiation.
- Transcriptomic landscape of early hair follicle and epidermal development
- TCF/Lef1-Mediated Control of Lipid Metabolism Regulates Skin Barrier Function
- Selective Expression of Calcium-Binding Proteins S100A8 and S100A9 at Distinct Sites of Hair Follicles
- New developments in the molecular treatment of ichthyosis: review of the literature
- Skin-associated adipocytes in skin barrier immunity: A mini-review
- Alkaline Ceramidase 1 Protects Mice from Premature Hair Loss by Maintaining the Homeostasis of Hair Follicle Stem Cells
- Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro
- Epidermal stem cells: skin surveillance and clinical perspective
- Identification of novel glucocorticoid receptor-regulated genes involved in epidermal homeostasis and hair follicle differentiation
- Trichofolliculoma: a rare variant of hair follicle hamartoma
- Comprehensive RNA sequencing in primary murine keratinocytes and fibroblasts identifies novel biomarkers and provides potential therapeutic targets for skin-related diseases