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Small molecules KY19382 and KY19334 may help treat skin cancer by reducing CDK1 levels and blocking harmful cell signals.

Certain gene variations increase the risk of alopecia areata in Koreans.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Mice with extra PKCδ resist chemical-induced skin cancer but not UV-induced.

A new keratin gene was found in mice, explaining hair growth.

Gene expression affects fur development in rex rabbits.

Key genes affect cashmere quality differences between Jiangnan and Changthangi goats.

Hoxc genes control hair growth through Wnt signaling.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

The Foxn1(-/-) phenotype disrupts hair growth and affects skin stem cells.

Gene regulatory regions evolve faster than protein coding regions, allowing new gene relationships without changing transcription factors.

Cashmere quality differences are due to gene expression variations affecting hair development and adaptation to cold.

KRT80 may worsen cancer by increasing growth and spread, but its full effects on treatment and outcomes need more research.

Pmg-1 and Pmg-2 are new genes important for skin and mammary gland development.

Keratinocytes can reduce the survival of certain melanoma cells, suggesting new therapy paths.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

61 functional keratin genes were identified in dogs and horses, leading to updated gene annotations.

Different keratins have unique expression patterns in mouse skin cells.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

A specific RNA, circNlgn, contributes to heart damage and scarring caused by the cancer drug doxorubicin.

OCIAD2 and DCN genes affect hair growth in goats by having opposite effects on a growth signaling pathway and inhibiting each other.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

Mutations in the Whn gene affect hair keratin gene expression differently.