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Mouse profilaggrin helps in skin cell differentiation and may be involved in calcium signaling.

Retinoic acid affects skin and hair health by working with specific receptors, and its absence can lead to hair loss and skin changes.

A gene mutation in mice causes permanent hair loss and skin issues.

Astrotactin-2 is cleaved in a specific way that helps understand its maturation.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

Overexpressing 14-3-3σ in mice skin reduces cell growth and hair density.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Cathepsin L deficiency causes hair and skin issues in mice.

A child with a rare vitamin D-resistant condition improved with treatment.

DKK proteins could help diagnose and treat various non-cancerous diseases.

Ca_v1.2 affects hair growth and could be a target for hair loss treatments.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

A boy with severe Vitamin D-resistant rickets did not respond to treatment and lacked a common symptom, suggesting a need for alternative treatments.

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

PP2Acα is essential for proper hair and skin development.

Vitamin D receptor is key to hair growth, not vitamin D itself.

A specific gene mutation causes sparse, brittle hair in a family.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

Trypsin slows hair growth and affects color by causing cell death in hair follicles.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

A virus protein can activate a pathway that may lead to abnormal hair follicle development.

Balding scalps show different gene expressions affecting hair growth compared to non-balding scalps.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requires high doses of calcium and vitamin D for management.

A substance called Vascular Endothelial Growth Factor can protect certain hair follicle stem cells from damage caused by androgens, suggesting a new possible treatment for hair loss.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

A specific mutation in PA-PLA1α causes abnormal hair growth.

Vitamin C derivative reduces hair loss-related protein in cells.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.