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Research 421–450 of 649
- Porokeratotic adnexal ostial nevus: a paradigm of cutaneous mosaicism
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Pioneers in Dermatology and Venereology: An Interview with Professor Danilo V. Stevanovic
- Faculty Opinions recommendation of Loss of desmocollin 3 in mice leads to epidermal blistering.
- The therapeutic efficacy of mesenchymal stem cells and their extracellular vesicles in the treatment of diverse skin diseases
- Fibroblasts: Origins, definitions, and functions in health and disease
- JAK inhibitors in dermatology: The promise of a new drug class
- Cutaneous and Mucosal Lichen Planus: A Comprehensive Review of Clinical Subtypes, Risk Factors, Diagnosis, and Prognosis
- 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
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- 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
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- 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
- RASopathic Skin Eruptions during Vemurafenib Therapy
- 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