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Research 61–90 of 1000+
- Peptidylarginine Deiminase Isoforms Are Differentially Expressed in the Anagen Hair Follicles and Other Human Skin Appendages
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Vitamin D and skin diseases: A review
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- 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
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- 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
- <i>In vivo</i> response of GsdmA3<sup>Dfl</sup>/+ mice to topically applied fish oil – effects on cellular markers and macrophages
- First Symposium of Ichthyosis Experts
- Skin, Genetic Defects, and Aging
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- Genes of Congenital Dermatologic Disorders in Dogs—A Review
- Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro
- [Association of a pediatric bullous eruption, cutaneous and muscular atrophy, hyperpigmentation and dysmorphism. A new entity?].
- A rare case of woolly hair with unusual associations
- Cutaneous Mastocytosis Associated With Congenital Alopecia
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Line-Field Optical Coherence Tomography: Usefulness in the Non-Invasive Differential Diagnosis of Congenital Alopecia of Infancy
- Early Diffuse Alopecia in a Neonate with Congenital Syphilis