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Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

CTCF protein is essential for skin and hair follicle development in mice.

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

A missing mK6irs1 gene causes hair loss in mice.

A woman with undifferentiated connective tissue disease was diagnosed with renal amyloidosis and carpal tunnel syndrome.

CRABP1 boosts hair cell growth in Hu sheep by affecting key genes.

Certain genes and proteins may help diagnose and treat primary cicatricial alopecia.

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

The study found nine new hair protein genes in human hair follicles.

A herbal extract may help treat certain types of hair loss by reducing a specific gene's activity.

CCCA is a common hair loss condition in African American women, often inherited and influenced by hairstyling, with unique scalp features detectable by special tools.

sPLA2-IIA increases growth in hair follicle stem cells and cancer cells, suggesting it could be targeted for hair growth and cancer treatment.

Targeting NCoR1 can help treat heart enlargement and dysfunction.

A boy's hair turned red because of genetic mutations, not lack of zinc.

Angiotensin II is found at higher levels in black sheep skin and may influence coat color.

A specific gene variant may increase the risk of developing Alopecia Areata.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

The study suggests that changes in immune system receptors and their interaction with a cell component may be important in the development of a type of hair loss condition.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Cronkhite-Canada Syndrome often leads to death within 6-18 months.

Trichohyalin is modified by enzymes to form strong structures in hair cells.

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

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.