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RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Keratins are important for skin cell health and their problems can cause diseases.

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

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

A mutation in the Sgkl gene causes defective hair growth in mice.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

TRα and CRABPII genes change their activity levels during goat fetal skin development.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

Inward rectifier potassium channels are important in many body functions and diseases, and could be potential drug targets.

Krt15+ cells in the mouse intestine resist radiation and can start tumors.

K31 can identify clear secretory cells in human sweat glands.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Keratin 15 helps maintain skin cell growth and repair.

Fatty acid transport protein 4 is essential for skin and hair development.

Mouse and human keratin 16 can both form filaments, with differences likely due to the tail domain, not the helical domain.

Esrp1 is important for skin health by helping form and maintain the skin barrier.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

Certain gene combinations improve cashmere quality and production in Liaoning goats.

Researchers found a new mutation causing total hair loss from birth.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.