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MCHR2 gene duplications may be linked to alopecia areata.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

A specific gene variation increases the risk of high uric acid and cholesterol in young Mexican males.

Mice with the ab gene have abnormal sebaceous gland development, affecting sebum production.

A certain gene variation can affect protein production and is linked to male pattern baldness.

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

ACBP is essential for healthy skin and fur by maintaining the skin's barrier function.

A new gene mutation causes a rare type of hair loss.

The ABCG2 gene variant increases the risk of high uric acid and cholesterol, especially in overweight or obese young Mexican males.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

PP2Acα is essential for proper hair and skin development.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Scientists found a new protein, AMY117, common in Alzheimer's patients, which could be important for treatment and diagnosis.

Hair loss gene found on chromosome 3q26.

BAF200 is essential for proper heart and coronary artery formation.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

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

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

CD2 might be a new treatment target for patchy alopecia areata.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

CCCA in women of African ancestry may be caused by PADI3 gene mutations and intense hair grooming.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

Blocking the protein CXCL12 with a specific antibody can increase hair growth in common hair loss conditions.

Certain gene variations may increase the risk and severity of alopecia areata.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.