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A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

High levels of sodium fluoride harm hair growth, but sodium selenite can reduce this harm.

Protein Kinase Cε increases skin sensitivity to UV damage and skin cancer risk.

Cell junctions are crucial for healthy skin by supporting sebaceous gland function and sebum production.

The nanohybrid system significantly improved wound healing and showed strong antibacterial activity.

Altering SSAT affects fat metabolism and body fat in mice.

High doses of some selenium supplements caused liver and reproductive harm in rats.

Mouse skin can produce and process serotonin, with variations depending on hair cycle, body location, and mouse strain.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

Mutations in keratin genes cause cell fragility and various skin disorders.

Clq deficiency is linked to systemic lupus erythematosus symptoms.

Skin surface lipids are important for skin health and altering them could help prevent aging and treat skin conditions.

Defective protein folding due to a mutation is key in ANE syndrome.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

The method shows how hair lipids form specific patterns and their roles in hair structure.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

High homocysteine levels in lupus may increase inflammation and cardiovascular risk.

The scraggly mutation causes hair loss and skin defects in mice.

Methionine restriction works better than betaine for treating CBS deficiency symptoms in mice.

Certain proteins are significantly increased in the skin of people with hidradenitis suppurativa.

Ceramide synthase 4 deficiency in mice leads to hair loss due to altered sebum lipids.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

The ZIP13 variant is linked to abnormal hair quality.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

Keratin from chicken feathers can be safely used on damaged skin.