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Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Pig skin cells can turn into mesodermal cells but lose their ability to become neural cells.

Hairless mammals evolved quickly in both gene and non-gene areas related to skin and hair.

Keratin mutations cause skin diseases and could lead to new treatments.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

Transgenic sheep cells with spider silk gene were successfully created for future sheep hair expression.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Meis2 is essential for touch sensation and proper nerve connection to touch receptors in certain skin areas of mice.

Increasing miR-149 reduces hair follicle stem cell growth and hair development by affecting certain cell growth pathways.

Hairless mice have longer hair follicles and abnormal structures during the catagen phase.