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Research 271–300 of 386
- Significance of stress keratin expression in normal and diseased epithelia
- Hair Shaft Abnormalities – Clues to Diagnosis and Treatment
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Complete Structure of an Epithelial Keratin Dimer: Implications for Intermediate Filament Assembly
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Keratins 6, 16, and 17 in Health and Disease: A Summary of Recent Findings
- Ichthyosis with confetti: clinics, molecular genetics and management
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Genetic Hair Disorders: A Review
- Regionalisation of the skin
- Menopause, skin and common dermatoses. Part 2: skin disorders
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation
- Molecular determinants for the chemical activation of the warmth-sensitive TRPV3 channel by the natural monoterpenoid carvacrol
- The Genetics of Human Skin Disease
- Utilities of Botulinum Toxins in Dermatology and Cosmetology
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- New developments in the molecular treatment of ichthyosis: review of the literature
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Evolution of Trichocyte Keratins
- Keratosis follicularis spinulosa decalvans in a female
- Ferulic Acid Induces Keratin 6α via Inhibition of Nuclear β-Catenin Accumulation and Activation of Nrf2 in Wound-Induced Inflammation