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Melanocyte-associated antigens may play a key role in alopecia areata and could be targets for new treatments.

New therapy helps treat hair loss.

The nutritional supplement Pilopeptan® WOMAN improved hair growth and thickness in women with hair loss.

The enzyme 5α-reductase is important for proper blood vessel development during the fertility-related transformation of the uterus lining.

A new topical treatment for hair loss shows strong hair growth effects with low toxicity.

Ginseng and Albizia extracts may help prevent age-related hair thinning.

Higher FABP4 levels may help diagnose androgenetic alopecia early.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

3α-androstanediol helps reduce age-related cognitive and mood declines in male rats, unlike testosterone.

A reliable method was developed to measure aristolochic acid-I in rat blood.

No link found between specific genes and female pattern hair loss.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

Neurosteroids affect prolactin levels in sheep differently depending on stress and pregnancy conditions.

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

A mutation in the KRT75 gene causes frizzle feathers in chickens.

RhoA helps skin stem cells grow, aiding wound healing.

Ritlecitinib is generally safe for alopecia areata patients over 72 months.

Androgen receptor abnormalities may contribute to hair loss in androgenetic alopecia.

Two new compounds were found to build bone and muscle without affecting reproductive organs and skin oil glands.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

AGA is caused by genetics and androgens, treatable with finasteride and minoxidil.

Glycyrrhiza glabra extract may prevent hair loss like finasteride.

Certain fats in the blood are linked to an increased risk of male pattern baldness.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Researchers developed new compounds that target the androgen receptor effectively with fewer side effects.

PDGFC gene may help select goats with desirable curly wool traits.