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Finasteride may treat baldness but less effective for those with 5α-reductase deficiency.

The body's change of testosterone into DHT is not necessary for testosterone's muscle and sexual effects.

Androgens like testosterone affect hair growth and oil production differently across body parts and individuals.

Male hormones affect oil-producing skin cells differently based on their body location, and the drug spironolactone can reduce these effects.

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

Avicequinone C, a compound found in the Avicennia marina plant, can reduce hair loss by inhibiting a hormone linked to androgenic alopecia.

A new plant extract from Avicennia marina could potentially be used to treat common hair loss.

The new compounds moderately block a specific enzyme and strongly counteract a male hormone, suggesting potential for treating certain male-related health conditions.

Low dose finasteride decreases certain steroids, possibly increasing depression risk.

Testosterone increases muscle mass regardless of DHT conversion blocking.

Exposure to finasteride in the womb caused lasting reproductive issues in male rats.

Androgens can both promote and prevent hair growth due to differences in gene expression in hair follicles.

Steroid sex hormones activate matriptase in prostate cancer cells but not in breast cancer cells.

Too much AKR1C3 enzyme causes resistance to finasteride by increasing testosterone.

Finasteride reduces inflammation and improves immune response after trauma by altering hormone levels.

New treatments for prostate cancer and BPH show promise, including novel compounds that target hormone synthesis and response.

Minocycline may cause hair loss by increasing DHT levels, but finasteride can help counteract this effect.

Using two drugs together, Flutamide and 4-MA, is more effective for blocking male hormones than using each one alone.

Finasteride doesn't affect ovulation in normal women.

The chapter explains the causes of excessive hair growth and masculinization in women and how to measure hormone levels related to these conditions.

Male genital development is driven by androgen signaling and understanding it could help address congenital anomalies.

Germacrone from Curcuma aeruginosa may help treat conditions related to male hormones by blocking a specific enzyme.

The enzyme that changes testosterone to a stronger form is mostly found in the part of the hair follicle called the dermal papilla.

New pregnane derivatives are effective at inhibiting an enzyme linked to hair loss and reducing oil gland activity.

Different skin cells process testosterone differently, and certain drugs can change this process, possibly helping treat acne and hair loss.

Different halogens on progesterone derivatives can either block or mimic male hormone effects, depending on their type and amount.

MENT could be a better option than testosterone for male hormone therapy and birth control because it works well at lower doses and has fewer side effects on the prostate.

Thyroid hormones and androgens affect gene expression in frog reproductive organs differently between males and females.

Testosterone helps human pancreatic cells increase insulin release.

Testosterone and some of its forms can strongly stimulate oil gland growth in skin.