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Research 571–600 of 788
- Stratum corneum dysfunction in dandruff
- Towards Dissecting the Pathogenesis of Retinoid-Induced Hair Loss: All-Trans Retinoic Acid Induces Premature Hair Follicle Regression (Catagen) by Upregulation of Transforming Growth Factor-β2 in the Dermal Papilla
- Natural killer cells in atopic and autoimmune diseases of the skin
- Tyrosine Kinases in Autoimmune and Inflammatory Skin Diseases
- Changing Patterns of Localization of Putative Stem Cells in Developing Human Hair Follicles
- Prevention and management of dermatological toxicities related to anticancer agents: ESMO Clinical Practice Guidelines☆
- Activation of Nrf2 in keratinocytes causes chloracne (MADISH)‐like skin disease in mice
- Adipocytes in Skin Health and Disease
- Histologic Changes in the Skin of Hairless Mice Following Peeling With Salicylic Acid
- Topical Retinoids: Therapeutic Mechanisms in the Treatment of Photodamaged Skin
- Human hair shaft proteomic profiling: individual differences, site specificity and cuticle analysis
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- The itchy scalp - scratching for an explanation
- Notch Signaling Regulates Late-Stage Epidermal Differentiation and Maintains Postnatal Hair Cycle Homeostasis
- Steroid Sulfatase in the Human Hair Follicle Concentrates in the Dermal Papilla
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Existence of trichohyalin-keratohyalin hybrid granules: Co-localization of two major intermediate filament-associated proteins in non-follicular epithelia
- Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- Vitamin D and skin diseases: A review
- Significance of stress keratin expression in normal and diseased epithelia
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Hair Growth Defects in Insig-Deficient Mice Caused by Cholesterol Precursor Accumulation and Reversed by Simvastatin
- Complete Structure of an Epithelial Keratin Dimer: Implications for Intermediate Filament Assembly
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty
- Psychological interventions in the management of common skin conditions
- Quality of life in children and adolescents with alopecia areata—A systematic review