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Research 661–690 of 859
- Nanoparticles for Topical Application in the Treatment of Skin Dysfunctions—An Overview of Dermo-Cosmetic and Dermatological Products
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Stratum corneum dysfunction in dandruff
- 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
- Trichoscopy in genetic hair shaft abnormalities
- Histologic Changes in the Skin of Hairless Mice Following Peeling With Salicylic Acid
- Topical Retinoids: Therapeutic Mechanisms in the Treatment of Photodamaged Skin
- 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
- 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