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This study found that the hair interior defect in AKR/J mice is linked to a mutation in the Soat1 gene, which disrupts SOAT1 protein expression and affects lipid metabolism critical for normal hair formation.

This case report describes a woman with systemic lupus erythematosus who developed non-progressive visual field defects after hypertensive retinopathy, with cotton wool spots indicating retinal nerve fiber microinfarctions.

This article discusses reconstructive challenges following Mohs micrographic surgery on the forehead and reports no new clinical results, illustrating techniques applicable to this region.

This article provides a diagnostic guide for clinicians to differentiate between various hair shaft disorders by using a structured question-by-question approach but does not report new clinical findings.

Proteomic analysis can identify genetic differences in mouse hair, helping understand hair defects and variations.