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Keratin-associated proteins have ancient origins and were used for different purposes before being adapted for hair in mammals.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Deleting MED1 in skin cells causes hair loss and skin changes.

α-parvin is necessary for skin and hair growth and for the correct orientation of skin cells.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Gene expression in wool follicles changes with growth cycles, offering insights into wool and human hair growth.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

A substance called DKK-1 increases in balding areas and causes hair cells to die when exposed to DHT.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

TMPRSS6 is crucial for controlling hepcidin and normal iron absorption.

The Hr protein binds to DNA, interacts with p53, and affects cell cycle genes.

Hair proteins change location and structure as hair cells mature.

A Korean girl developed kinky hair without known cause or effective treatment.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

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

A gene mutation causes monilethrix in a Chinese family.

Immortalized human dermal papilla cells were created that grow better and can still help form hair.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Keratin 15 helps keep skin cells in a young, undifferentiated state.

Keratin-associated protein nanoparticles from human hair may help stop bleeding quickly and safely.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Dkk4 is necessary for the initial development and arrangement of hair follicles.

New mutations in the hairless gene may cause hair loss and affect bone development.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

The KRTAP22-2 gene in sheep does not significantly affect wool traits.