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Research 571–600 of 1000+
- The influence of vitamin C deficiency on dermatosis in neonatal dairy calves
- Alopecia difusa e atrofia da tireoide associadas à deficiência de selênio e zinco em ovinos.
- Cicatricial Alopecia with Particular Trichoscopic and Histopathological Features
- The Effects of Avocado Extract (Persea americana mill), Papaya Seed (Carica papaya l.), and Celery (Apigium graveolens l.) Combination on The Skin and Hair of Mice (Rattus novergicus)
- 732 Ceramide synthase 4 controls epidermal lipid composition and barrier function
- 489 Seborrhea-like dermatitis phenotype in the Mpzl3 knockout mice
- Skin, Genetic Defects, and Aging
- Redox-directed interventions targeting skin photodamage
- The dark and the bright sides of the transcription factor Nrf2 in skin protection and disease (Nrf2 and epidermal barrier function)
- Verrucous hemangioma leg: A challenging birthmark
- Erythema Multiforme Like Lesions in a Case of Systemic Lupus Erythematosus
- Self-cured Flank Alopecia in a Dog
- Células-tronco foliculares e aspectos histopatológicos cutâneos tardios após prolongada remoção de pêlos a laser
- Case of epidermolytic ichthyosis (bullous congenial ichthyosiform erythroderma) with a novel L157P mutation in KRT10 complicated by hypercalcemia
- The Roles of Smad2 and Smad3 in Mouse Skin Development
- Viewpoint 2
- Chronic Toxicity Studies of the Potential Cancer Preventive 2-(Difluoromethyl)-<i>dl</i>-ornithine
- Hair Dye Effects on the Hair Coat and the Skin of the Dog: A Scanning Electron Microscopic Study
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- Disturbed Epidermal Structure in Mice with Temporally Controlled Fatp4 Deficiency
- Lichen Spinulosus: Case Report and Review of Literatures
- A comedonal variant of chronic cutaneous lupus erythematosus: Case report and literature review
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Circle hairs involving the extremities in a young girl
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Śródskórne iniekcje acetonidu triamcynolonu w leczeniu Zespołu Grahama-Little’a — opis przypadku
- Obesity and the skin
- Impaired Notch‐MKP‐1 signalling in hidradenitis suppurativa: an approach to pathogenesis by evidence from translational biology