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

Finasteride reduces sperm count and affects male reproductive function, while Epristeride does not.

Human liver enzyme DHEA ST helps process minoxidil.

Finasteride changes androgen receptor location in rat epididymis without altering tissue structure.

Some new progesterone derivatives are better at blocking testosterone conversion than a common drug.

New compounds show promise for treating hair loss, enlarged prostate, and prostate cancer, with some being more effective and having different side effects than current treatments.

Researchers found new potential treatments for conditions related to the androgen receptor, like male hormonal contraception, by testing thousands of compounds.

DHEA inhibits growth in both mouse and human melanoma cells but works differently in each.

Oestrogen does not affect adrenal androgen levels in children and adolescents.

Mimicking the steroid A-ring may help create effective enzyme inhibitors for prostate disease treatment.

Androstanediol glucuronide is a reliable marker for hirsutism in women.

Scientists found new nonsteroidal compounds that can act like natural male hormones and might help treat male fertility and hormone issues.

ERβ has potential in treating prostate cancer and neurodegenerative diseases, but human studies are needed before clinical use.

Male sexual differentiation is regulated independently, while female differentiation occurs in an androgenic environment, affecting conditions like congenital adrenal hyperplasia.

Higher testosterone and DHEA-S levels may be linked to male pattern baldness.

Cyproterone acetate effectively treats sexual disorders by reducing sexual functions and is generally well-tolerated.

Testosterone and DHEA can benefit women's health but must be prescribed carefully due to potential risks.

Cyproterone Acetate effectively treats androgen-related conditions and is used in prostate cancer therapy and hormone therapy for transgender women.

Finasteride may affect female fertility by altering gene activity.

Epristeride's metabolism involves key metabolites and proteins, affecting its use in doping tests.

New steroidal compounds could be effective for treating conditions related to 5α-reductase enzyme activity.

New genes and pathways are important for testosterone production and male sexual development.

Finasteride, when taken daily, lowers dihydrotestosterone levels but doesn't noticeably affect adrenal steroid production, except by blocking the 5 alpha-reductase enzyme.

DHEA improved brain function and behavior in old monkeys and had additional health benefits.

Reducing 5α-reductase activity helps endometrial cells differentiate, aiding pregnancy.

Girls have higher DHEA levels earlier in puberty than boys, indicating earlier development.

Certain progesterone derivatives can inhibit enzymes and reduce androgenic activity, potentially affecting prostate growth.

Beard hair follicles convert testosterone to 5α-dihydrotestosterone most intensively.