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Research 241–270 of 397
- Human Eccrine Sweat Gland Cells Can Reconstitute a Stratified Epidermis
- Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Patterns of desmocollin synthesis in human epithelia: immunolocalization of desmocollins 1 and 3 in special epithelia and in cultured cells.
- Stratum corneum dysfunction in dandruff
- Natural killer cells in atopic and autoimmune diseases of the skin
- Tyrosine Kinases in Autoimmune and Inflammatory Skin Diseases
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- The molecular basis of human keratin disorders
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Histologic Changes in the Skin of Hairless Mice Following Peeling With Salicylic Acid
- Dupilumab in Inflammatory Skin Diseases: A Systematic Review
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- Peptidylarginine Deiminase Isoforms Are Differentially Expressed in the Anagen Hair Follicles and Other Human Skin Appendages
- Environmental Air Pollutants Affecting Skin Functions with Systemic Implications
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Proinflammatory cytokines regulate epidermal stem cells in wound epithelialization
- Unmet Medical Needs in Chronic, Non-communicable Inflammatory Skin Diseases
- Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses
- Lineage Analysis of Epidermal Stem Cells
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Telogen effluvium: a comprehensive review
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Keratins 1 and 10 or homologues as regular constituents of inner root sheath and cuticle cells in the human hair follicle.
- Disruption of Smad4 in Mouse Epidermis Leads to Depletion of Follicle Stem Cells
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- Development of Hair Fibres
- The Role of Nutrition in Immune-Mediated, Inflammatory Skin Disease: A Narrative Review