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RPGRIP1L helps skin cells stick together by blocking PKCβII, which can prevent skin blistering like in pemphigus.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps from birth.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

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

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

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

Too much IKZF1 and Ikaros protein may cause alopecia areata.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

FOXN1 duplication can cause excessive hair growth.

K6 gene expression can be controlled and manipulated in mice for studying skin disorders.

PSAT1 is key for hair growth and stem cell function in cashmere goats.

Hair loss in certain mice is linked to changes in keratin-related genes.

Hair proteins change location and structure as hair cells mature.

Too much keratin 16 in mice skin causes abnormal skin thickening and structure.

CAP1 helps Arabidopsis plants grow better under ammonium stress.

A new keratin 6 type in mice explains why some mice without certain keratin genes still have normal hair and nails.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

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

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

A mutation in the KRT25 gene causes woolly hair and hair loss.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Laminin-511 is crucial for early hair growth and maintaining important hair development signals.

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

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

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