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Research 181–210 of 226
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Chronic graft versus host disease and skin
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- Trichoscopy as a diagnostic tool in trichorrhexis invaginata and Netherton syndrome
- Ingestion of a dietary supplement resulting in selenium toxicity
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Genetic Hair Disorders: A Review
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Cyclic Alopecia and Abnormal Epidermal Cornification in Zdhhc13 -Deficient Mice Reveal the Importance of Palmitoylation in Hair and Skin Differentiation
- Efficient In Vitro Transfection of Human Keratinocytes with an Adenovirus-Enhanced Receptor-Mediated System
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- Iron Metabolism of the Skin: Recycling versus Release
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Hair follicles modulate skin barrier function
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Frontal fibrosing alopecia: a review of eleven patients
- A rare complication of follicular hair unit extraction: Kaposi’s varicelliform eruption
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Medical Dermatology
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex