Search
for
Sort by
Research 121–150 of 227
- 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
- Off-label uses of retinoids in dermatology
- Lamellar ichthyosis, dwarfism, mental retardation, and hair shaft abnormalities
- Chronic graft versus host disease and skin
- Hodgkin′s lymphoma presenting as alopecia
- Netherton Syndrome – Responding to Oral Retinoids
- An Unusual Case of Mycosis Fungoides Presenting with Multiple Atypical Morphologies in a Photoexacerbated Distribution
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- Proteome Analysis of Human Hair Shaft
- 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
- Trichoscopy in genetic hair shaft abnormalities
- Dupilumab in Inflammatory Skin Diseases: A Systematic Review
- 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
- 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
- Psychological interventions in the management of common skin conditions
- 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
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16