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A protein called ectodysplasin-A2 increases a hair growth inhibitor in balding cells, which could be a target for hair loss treatment.

The enzyme Dgat1 is essential for healthy hair and skin by controlling retinoid levels.

The hr gene is linked to hair loss in Valle del Belice sheep.

Vitamin D and its receptor regulate skin functions like cell growth, immunity, hair cycle, and tumor prevention.

Dopaminergic neurons in the gut have distinct subtypes, some releasing both dopamine and acetylcholine.

Lhx2 helps retinal cells respond to signals for eye development.

Urotensin II increases growth and VEGF production in rat skin cells by turning on the Wnt-β-catenin pathway.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.

VR1 signaling can inhibit hair growth by affecting cell processes and increasing hair growth inhibitors.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

Measuring 24-OHase induction helps identify defects in vitamin D processing and predict treatment response.

CD2 might be a new treatment target for patchy alopecia areata.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

A specific gene variant may increase the risk of developing Alopecia Areata.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

DORN1 receptor affects eATP-induced stomatal changes but not eADP in Arabidopsis thaliana.

Only one K16 gene on chromosome 17 makes a functional keratin protein.

Certain gene variations may increase the risk and severity of alopecia areata.

Defects in certain proteins cause major heart abnormalities during early development.

A specific gene mutation causes congenital hair loss.

Blocking a protein called prostaglandin D2 might help treat hair loss.

Two new gene mutations cause a rare hair disorder.

Lhx2 is essential for effective Sonic Hedgehog signaling in early retinal development.

Different keratins have unique expression patterns in mouse skin cells.