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Research 571–600 of 1000+
- The Non-Cosmetic Dermatological Use of Botulinum Neurotoxin
- TONGUE, RED
- Fibroblasts: Origins, definitions, and functions in health and disease
- JAK inhibitors in dermatology: The promise of a new drug class
- Hidradenitis suppurativa: pathogenesis and management
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- Expression of Hypothalamic–Pituitary–Thyroid Axis RelatedGenes in the Human Skin
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- The use of cyclosporine in dermatology: Part I
- Type XVII collagen coordinates proliferation in the interfollicular epidermis
- TRP Channels in Skin Biology and Pathophysiology
- Cytochrome P450: A Target for Drug Development for Skin Diseases
- Cutaneous manifestations and considerations in COVID ‐19 pandemic: A systematic review
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- 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
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Keratins and disease at a glance
- 308-nm excimer laser therapy in alopecia areata
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- The molecular basis of human keratin disorders
- The Two Functional Keratin 6 Genes of Mouse Are Differentially Regulated and Evolved Independently from Their Human Orthologs
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Rapidly progressing mycosis fungoides presenting as follicular mucinosis
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- Dupilumab in Inflammatory Skin Diseases: A Systematic Review
- Environmental Air Pollutants Affecting Skin Functions with Systemic Implications