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Research 421–450 of 484
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Hair follicle–derived IL-7 and IL-15 mediate skin-resident memory T cell homeostasis and lymphoma
- The IL-23/IL-17 Pathway in Inflammatory Skin Diseases: From Bench to Bedside
- Proteome Analysis of Human Hair Shaft
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Changing Patterns of Localization of Putative Stem Cells in Developing Human Hair Follicles
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- The molecular basis of human keratin disorders
- Peptidylarginine Deiminase Isoforms Are Differentially Expressed in the Anagen Hair Follicles and Other Human Skin Appendages
- New clinico‐genetic classification of trichothiodystrophy
- 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
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- 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
- Hair Shaft Abnormalities – Clues to Diagnosis and Treatment
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- Psychological interventions in the management of common skin conditions
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- Eyebrow Loss
- 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
- The Genetics of Human Skin Disease
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Equine Epidermis: A Source of Epithelial-Like Stem/Progenitor Cells with In Vitro and In Vivo Regenerative Capacities