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Research 571–600 of 810
- “Degeneration” in Dermatopathology
- Madarosis and facial keratinaceous spines
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Comparative study of cutaneous manifestations in patients with chronic kidney disease , patients on haemodialysis, and renal transplant recipients
- Trichothiodystrophy in a child with occult learning disorder
- Cross‐linked features of mouse pelage hair resistant to detergent extraction
- Analysis of the abnormal human hair keratins by two-dimensional polyacrylamide gel electrophoresis
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Hydrobiome of Thermal Waters: Potential Use in Dermocosmetics
- Adult-onset porokeratotic eccrine ostial and dermal duct nevus:dermatoscopic findings and treatment with tazarotene
- Erythroderma: clinical and etiological study of 88 cases seen in a tertiary hospital over 25 years
- Cell death by cornification
- Cutaneous and Mucosal Lichen Planus: A Comprehensive Review of Clinical Subtypes, Risk Factors, Diagnosis, and Prognosis
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Glycerol Regulates Stratum Corneum Hydration in Sebaceous Gland Deficient (Asebia) Mice
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Lack of the Vitamin D Receptor is Associated with Reduced Epidermal Differentiation and Hair Follicle Growth
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- Matriptase: Potent Proteolysis on the Cell Surface
- Cannabinoid Signaling in the Skin: Therapeutic Potential of the “C(ut)annabinoid” System
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- Genetic architecture of mouse skin inflammation and tumour susceptibility
- Intracrine androgen biosynthesis, metabolism and action revisited
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- Type XVII collagen coordinates proliferation in the interfollicular epidermis
- Human Peptidylarginine Deiminase Type III: Molecular Cloning and Nucleotide Sequence of the cDNA, Properties of the Recombinant Enzyme, and Immunohistochemical Localization in Human Skin
- Nanoparticles for Topical Application in the Treatment of Skin Dysfunctions—An Overview of Dermo-Cosmetic and Dermatological Products
- Proteome Analysis of Human Hair Shaft
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome