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Research 361–390 of 745
- Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses
- Disorders of Keratinization
- A systematic method for the sensitive and specific determination of hair lipids in combination with chromatography
- Contribution of the Hair Follicular Pathway to Total Skin Permeation of Topically Applied and Exposed Chemicals
- Lead-revealed lipid organization in human hair
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair
- The acyl-CoA binding protein is required for normal epidermal barrier function in mice
- Lipedematous alopecia: an uncommon clinicopathologic variant of nonscarring but permanent alopecia
- Expression of MK6a dominant-negative and C-terminal mutant transgenes in mice has distinct phenotypic consequences in the epidermis and hair follicle
- Spiny keratoderma ‐ a demonstration of hair keratin and hair type keratinization
- Topical Administration of Drugs Incorporated in Carriers Containing Phospholipid Soft Vesicles for the Treatment of Skin Medical Conditions
- Developing stratified epithelia: lessons from the epidermis and thymus
- Phospholipase A2 in skin biology: new insights from gene-manipulated mice and lipidomics
- Chronic Treatment with Minoxidil Induces Elastic Fiber Neosynthesis and Functional Improvement in the Aorta of Aged Mice
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Distribution of keratin and associated proteins in the epidermis of monotreme, marsupial, and placental mammals
- Expression of MsPG3‐GFP fusions in <i>Medicago truncatula</i>‘hairy roots’ reveals preferential tip localization of the protein in root hairs
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Skin Development and Disease: A Molecular Perspective
- Cholesterol and Phospholipid-free Multilamellar Niosomes Regulate Transdermal Permeation of a Hydrophobic Agent Potentially Administrated for Treating Diseases in Deep Hair Follicles
- Hyperpigmented Upper Eyelid: A Clue to the Diagnosis of Facial Lichen Planus Pigmentosus in a Patient with Frontal Fibrosing Alopecia
- Human essential fatty acid deficiency: treatment by topical application of linoleic acid.
- PEO-b-PCL grafted niosomes: The cooperativilty of amphiphilic components and their properties in vitro and in vivo
- Clinical Description of Frontal Fibrosing Alopecia with Concomitant Lichen Planopilaris
- Self-consistent field theory for the interactions between keratin intermediate filaments
- The Fate of Epidermal Tight Junctions in the stratum corneum: Their Involvement in the Regulation of Desquamation and Phenotypic Expression of Certain Skin Conditions
- Hair and Scalp Disorders in a Tuscan Pediatric Dermatological Outpatient Clinic: A Clinical and Epidemiological Evaluation
- Hair follicles modulate skin barrier function
- Introduction—Human Hair, Skin, and Hair Care Products