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Research 391–420 of 517
- Dupilumab in Inflammatory Skin Diseases: A Systematic Review
- Peptidylarginine Deiminase Isoforms Are Differentially Expressed in the Anagen Hair Follicles and Other Human Skin Appendages
- New clinico‐genetic classification of trichothiodystrophy
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Unmet Medical Needs in Chronic, Non-communicable Inflammatory Skin Diseases
- Ethnodermatological use of medicinal plants in India: From ayurvedic formulations to clinical perspectives – A review
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- COVID‐19 and cutaneous manifestations: A review of the published literature
- Current Advanced Therapies Based on Human Mesenchymal Stem Cells for Skin Diseases
- Vitamin D and skin diseases: A review
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- Psychological interventions in the management of common skin conditions
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Madarosis: A marker of many Maladies
- Sarcoidosis: Are there differences in your skin of color patients?
- FOXN1 deficient nude severe combined immunodeficiency
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- Eyebrow Loss
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- A comprehensive review on invasomal carriers incorporating natural terpenes for augmented transdermal delivery
- Genetic Hair Disorders: A Review
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer