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Finasteride treatment changes urine metabolomics and steroid signatures, potentially monitoring effectiveness but may cause sexual side effects.

Androgen receptors play a key role in male development and prostate cancer, with treatments targeting androgen action.

11β-Hydroxylase inhibitors help prevent seizures in mice by boosting natural neurosteroid production.

Mice without the enzyme HSD17B3 still produce normal testosterone, suggesting they have different ways to make it compared to humans.

The method is quick and effective for testing steroid 5 alpha-reductase inhibitors.

Dutasteride mesotherapy can cause hair loss in some people.

Ergostadienol from Moringa seed oil may help prevent hair loss.

Finasteride effectively inhibits the enzyme steroid 5 alpha-reductase II.

Synthetic hormone treatment reduces melanin and hair growth in rats.

The compound (1R,2S)-4-(2-Cyano-cyclohexyl-oxy)-2-trifluoromethyl-benzonitrile can stimulate hair growth and reduce oil production when applied topically.

Dutasteride 0.5 mg works better than finasteride and placebo for increasing hair in men with hair loss.

Combining Minoxidil with topical Dutasteride via microneedling is the most effective and safe treatment for hair loss.

Diazoxide applied to the skin can increase hair growth without harmful side effects.

High levels of 3 alpha-diol glucuronide in the blood are a marker of increased androgen action in women with excessive hair growth of unknown cause.

Using anabolic steroids 'Sus' and 'Deca' for bodybuilding caused severe acne in a man.

Dutasteride is more effective than finasteride for hair loss treatment.

Androgens increase pigmentation in young hamsters, but estrogens can reverse this effect.

Cyproterone acetate is used to treat conditions like prostate cancer, early puberty, excessive sexual drive, and female androgenization by affecting androgen functions and suppressing certain hormones.

Desolvation of finasteride depends on environment and technique.

A substance called Compound 2g can strongly block STS (a hormone-related enzyme) without affecting estrogen levels, making it potentially good for treating breast cancer.

Piptadeniastrum africanum and Cordia plathytyrsa can increase testosterone without major metabolic changes, but may affect triglycerides and creatinine.

Finasteride's molecular properties and active sites were identified using computational methods.

Finasteride reduces DHT levels and affects gene expression in fish, similar to its effects in humans.

Finasteride is stable except in high pH, and lactose and magnesium stearate should be replaced in formulations.

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

The treatment reduced hair growth and testosterone in women with excess hair and had some effects on stress responses.

Hormone therapy for trans individuals is effective and generally safe in the short term.

In 2005, men used finasteride mainly to treat an enlarged prostate.

Cyproterone acetate treatment is safe and causes mild feminization, which increases with added estrogen.