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Research 451–480 of 764
- Ichthyosis
- Cutaneous Adnexal Cysts Revisited: What We Know and What We Think We Know
- Hydrogel-Forming Microneedles for Transdermal Drug Delivery
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Amplitude-guided deep reinforcement learning for semi-supervised layer segmentation
- The fatty acids and the skin: a focus on the n-6 family of unsaturated fatty acids
- Study of thin films and nanoparticles obtained by self-assembly of block copolymers and their interactions with an oligo / polysaccharide
- Etude de films minces et de nanoparticules obtenus par auto-assemblage de copolymères à blocs et leurs interactions avec un oligo/polysaccharide
- Porokeratotic Eccrine Ostial and Dermal Duct Nevus: A Report of Rare Late-Onset Solitary Lesion
- Three-dimensional microanatomy of mechanoreceptors and their possible mechanism of sensory transduction.
- Extensive Spiculated Follicular Porokeratosis With Alopecia: A Case Report
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- In situ tensile deformation characterization of human hair with atomic force microscopy
- 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
- 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
- Phospholipase A2 in skin biology: new insights from gene-manipulated mice and lipidomics
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- 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