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

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

KRT71 gene variants may influence camel hair shape but don't fully explain it.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

Changing YBX1 protein activity affects skin stem cell function and aging.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

ZPK helps skin cells mature and may affect skin health.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

K6hf is a unique protein found only in a specific layer of hair follicles.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Two new gene clusters important for hair formation were found on human chromosome 11.

ARHGEF3 is essential for proper hair follicle development.

Decorin helps hair cells grow and move, and keeps hair growth phase going in mice.

A new pair of mouse keratins, 65 kD and 48 kD, are found in specific skin areas and are linked to a unique skin differentiation type.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Finasteride helps female-pattern hair loss.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

PRC1 influences skin stem cell development by both turning genes on and off, affecting hair growth and skin cell types.

RXRa is crucial for Th2 immune cell development and may link nutrition to immune health.

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

Mice without certain skin proteins had abnormal skin and hair development.

People with non-scarring hair loss have higher levels of DKK-1, a protein linked to hair growth, than those with scarring hair loss or no hair loss.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.