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Research 211–240 of 668
- Cell death by cornification
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Therapeutic Use of Botulinum Neurotoxins in Dermatology: Systematic Review
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Keratins 6, 16, and 17 in Health and Disease: A Summary of Recent Findings
- Regionalisation of the skin
- The molecular basis of human keratin disorders
- Significance of stress keratin expression in normal and diseased epithelia
- The Important Role of Leptin in Modulating the Risk of Dermatological Diseases
- The Pressurized Skin: A Review on the Pathological Effect of Mechanical Pressure on the Skin from the Cellular Perspective
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Proceedings of the Ninth World Congress for Hair Research (2015)
- 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
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- TRP Channels in Skin Biology and Pathophysiology
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- 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
- Prevention and management of dermatological toxicities related to anticancer agents: ESMO Clinical Practice Guidelines☆
- 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 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