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Hoxc13 is important for hair and tongue development by controlling hair keratin genes.

Trps1 is essential for proper hair follicle development.

Removing UBE2N from skin cells causes inflammation and immune response, which can be lessened with specific inhibitors.

Introducing the OTC gene improved symptoms in mice with OTC deficiency.

Hair sensitivity to androgens is partly controlled by specific enzyme expressions in different hair areas.

Key genes and pathways involved in thyroid eye disease were identified, aiding potential treatment and diagnosis.

The Wave complex controls skin growth by suppressing certain signals.

ODC transgenic mice can model human hair loss with skin lesions.

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

Different androgen concentrations affect wool-related gene expression differently in Hetian and Karakul sheep breeds.

Rac1 is crucial for normal hair structure and pigmentation.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

LEF-1 boosts cell growth in goat hair follicles, aiding cashmere production.

Runx1 helps control the KAP5 gene in human hair follicles.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Dkk4 protein helps control how hair grows and its arrangement.

Foxc1 helps keep hair follicle stem cells inactive, preventing hair loss.

A single amino acid change in the vitamin D receptor can disrupt its function and lead to hair loss.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

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

LTBP1 is a key regulator in diseases and a potential target for new treatments.

Reducing FOXA2 in skin cells lowers their ability to grow hair.

The enzyme 5α-reductase type 1 is important for blood vessel development and fertility in the uterus.

SCD1 is important for hair growth by keeping the connection in skin cells where hair stem cells live stable.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

New findings suggest the protein linked to Birt–Hogg–Dubé syndrome is important in cell signaling and could affect treatment understanding.