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Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

Too much Smad7 changes skin and hair development by breaking down a protein called β-catenin, leading to more oil glands and fewer hair follicles.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Females with 5 alpha-reductase-2 deficiency have less body hair, no acne, normal fertility, and delayed menarche.

cDermo-1 causes dense skin, feathers, and scales in chickens.

Twist2 is essential for scarless skin healing and hair growth in mouse fetuses.

A new DSG4 gene mutation causes hair defects in a young girl.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

Rac1 is crucial for normal hair structure and pigmentation.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

Normal skin results from interactions between EGF and the Tabby mutation.

Arabidopsis Formin 2 stabilizes actin filaments to aid cell-to-cell trafficking.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

The 14-3-3σ gene is essential for preventing hair loss.

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

Increasing COX-2 in mouse skin causes bigger sebaceous glands and thinner hair, but stopping COX-2 can reverse hair thinning.

Tet1/2/3 enzymes affect hair follicle cell development by influencing BMP signaling.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

Researchers created a new mouse model for studying scleroderma.

A specific gene mutation causes complete hair loss in an Irish Traveller family.

Snail2 is crucial for hair growth and affects skin cancer development.

Runx1 is crucial for proper hair structure and development.