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Finasteride inhibits enzyme activity in rhesus macaques, suggesting they're useful for evaluating similar drugs.

Erythropoietin overexpression disrupts hair growth and fat formation in mice.

5% topical minoxidil improves hair density and quality in monilethrix patients.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Higher PHGDH levels cause unusual melanin buildup in hair follicles.

Msx2 is essential for proper enamel formation by preventing abnormal cell transformation.

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

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Targeting impaired Nrf2 signaling might help treat hidradenitis suppurativa early on.

Desmocollin 1 is essential for strong skin and proper skin function.

Copper treatments increase copper in all tissues, but brindled female mice accumulate much more copper in their kidneys without clinical effects, unlike brindled male mice where brain copper deficiency is clinically significant.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

Blocking a specific enzyme in male rat fetuses leads to the development of nipples and feminized genitalia.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Hedgehog signaling can create new hair follicles but may also cause tumors.

The fer-ts mutation in plants prevents root hair growth at high temperatures.

Increased ODC expression makes normally tumor-resistant mice more prone to tumor development.

Proper cell death regulation is crucial for normal hair follicle regeneration and skin remodeling.

The enzyme 5α-reductase type 1 is important for blood vessel development and fertility in the uterus.

Early skin biopsy is crucial for diagnosing Conradi-Hünermann-Happle syndrome.

PrrH sRNA controls pyochelin production in *Pseudomonas aeruginosa*.

A severe virus outbreak in yaks on the Qinghai-Tibet Plateau caused high death rates and requires targeted control measures.

Abnormal gene expression related to keratin causes hair loss in certain mice.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

Mirex seems to promote a unique group of skin cells different from those affected by another tumor promoter, TPA.

Nonclassic 21-hydroxylase deficiency is a common, treatable genetic disorder causing reversible symptoms like acne and hair loss.

The activity of a specific rat enzyme in the prostate and epididymis is highly dependent on the acidity level.

RORA plays a key role in controlling seasonal hair molting by affecting hair follicle cell activity.