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Different types of PCOS in Chinese Han women show varying levels of male hormone and metabolic issues.

Phytosterols may help manage prostate issues but are less effective than synthetic drugs.

Testosterone affects stress hormone levels differently in adolescent and adult male rats.

Women with nonclassic 21-hydroxylase deficiency can have successful pregnancies through IVF, with certain factors affecting their chances.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

The vitamin D receptor helps regulate skin and hair health independently of its usual vitamin D ligand.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

Hormonal therapies, especially antiandrogens, can help manage Hidradenitis Suppurativa.

Hair stem cells produce a protein called COL17A1 that plays a key role in their development and is linked to hair thinning and baldness.

Rodent models of PCOS show some similar and some different lipid changes compared to humans.

The method can measure multiple hormones in women's hair and may help identify hormone-related health issues.

A substance called compound-1 could help increase hair growth by maintaining prostaglandin levels in hair follicles.

Increased HIF-1α is linked to the inflammation and severity of hidradenitis suppurativa, suggesting treatments that lower HIF-1α could help.

5α-Reductase inhibitors can help treat hair loss, acne, and prostate issues by reducing DHT levels.

DHT deficiency in rats reduces sperm content and affects testis structure over time.

CB-03-01 is a promising skin cream for treating hormone-related skin problems without causing harmful body-wide effects.

New compounds may soon be tested to treat excessive hair growth in women.

Woodhouse-Sakati Syndrome can include unique symptoms like liver issues and low growth hormone.

Vitamin D receptor mutations can cause alopecia by affecting hair growth genes.

DHEA affects various tissues by interacting with multiple receptors and can be converted into sex hormones.

A woman with non-classic CAH had unusual heavy periods and high hormone levels, improved with treatment.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

The girl's unexpected pubic hair growth led to a diagnosis different from complete androgen insensitivity syndrome.

Researchers found new potential but less potent rat enzyme inhibitors using a 3D model.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

Urtica dioica extract may help treat androgenic skin diseases by reducing a specific gene's activity.

The vitamin D receptor is involved in multiple body functions beyond calcium regulation, including immune response and rapid reactions not related to gene activity.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

17β-estradiol may help hair growth by increasing cannabinoid receptor type 1.

A reliable model for screening type II 5α-reductase inhibitors was created and validated.