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Research 361–390 of 535
- Skin-infiltrating CD4+ lymphoma cells depend on hair follicle-derived IL-7
- Trichorrhexis Invaginata and Netherton’s Syndrome
- Genetics of Inherited Ichthyoses and Related Diseases
- The ultrastructure of the interfollicular epidermis of the hairless (hr/hr) mouse
- Discoid lupus erythematosus successfully treated with deucravacitinib
- 308-nm Excimer Lamp vs. Combination of 308-nm Excimer Lamp and 10% Liquor Carbonis Detergens in Patients With Scalp Psoriasis: A Randomized, Single-Blinded, Controlled Trial
- CD8+ mycosis fungoides clinically masquerading as alopecia areata
- An Overview of Growth Factors as the Potential Link between Psoriasis and Metabolic Syndrome
- The therapeutic efficacy of mesenchymal stem cells and their extracellular vesicles in the treatment of diverse skin diseases
- 0975 Single-cell transcriptomic profiling reveals distinct immunopathogenic programs in alopecia totalis/universalis compared to patchy alopecia areata
- New Topical Treatment for Psoriasis
- Psoriasis Research: A Comprehensive Review
- Madarosis from mitochondriopathy
- Connexin mutations in human disease
- 0441 Systemic autoimmune comorbidity in alopecia totalis and universalis compared with patchy alopecia areata: A retrospective cohort study
- Emerging Topical and Systemic JAK Inhibitors in Dermatology
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Hair follicle–derived IL-7 and IL-15 mediate skin-resident memory T cell homeostasis and lymphoma
- The IL-23/IL-17 Pathway in Inflammatory Skin Diseases: From Bench to Bedside
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- Proteome Analysis of Human Hair Shaft
- Cutaneous manifestations and considerations in COVID ‐19 pandemic: A systematic review
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Changing Patterns of Localization of Putative Stem Cells in Developing Human Hair Follicles
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- The molecular basis of human keratin disorders
- Trichoscopy in genetic hair shaft abnormalities
- Dupilumab in Inflammatory Skin Diseases: A Systematic Review
- Peptidylarginine Deiminase Isoforms Are Differentially Expressed in the Anagen Hair Follicles and Other Human Skin Appendages