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Testosterone boosts physical performance, grip strength, and lean body mass in older men with low testosterone.

Compounds 4, 4b, and 4c effectively inhibit an enzyme linked to testosterone conversion without significant toxicity.

The combination of cyproterone acetate and testosterone enanthate is highly effective in preventing sperm production and could be a good reversible male contraceptive.

Certain derivatives are more effective 5α-reductase type 2 inhibitors than finasteride.

A new antiandrogen compound was made and its detailed three-dimensional shape was described.

Dihydrotestosterone has a reduced effect on muscle-building in people with testicular feminization syndrome, especially after their gonads are removed.

Testosterone boosts red blood cell production and changes iron metabolism without needing dihydrotestosterone.

Testosterone increases 3α-androstanediol levels, which can be blocked by finasteride.

Testosterone is made by Leydig cells, is active when not bound to proteins, and works by binding to receptors in muscles and other tissues.

The procedure accurately measures 5-alpha-dihydrotestosterone in blood, useful for standard tests.

Testosterone increases muscle mass regardless of DHT conversion blocking.

The new oral testosterone pill normalized testosterone levels and lowered SHBG in men with low testosterone.

The document concludes that better biomarkers are needed to detect long-term oral testosterone use in athletes.

Some synthesized compounds were more effective than Finasteride in reducing prostate cancer cell growth and androgen levels.

Testosterone replacement therapy helps manage deficiency and has various methods, but requires careful monitoring to avoid side effects.

Testosterone implants in women require pharmacological dosing to be effective and are generally safe and well-tolerated.

The guideline recommends mental health involvement in diagnosing gender identity disorder and outlines hormone and surgical treatment protocols, emphasizing safety, informed consent, and long-term monitoring.

Dehydroepiandrosterone (DHEA) is a prohormone important for producing sex steroids and has potential health benefits.

The Endocrine Society advised against routine testosterone therapy for women, citing a need for more research on long-term safety and a clear definition of androgen deficiency.

The guidelines advise against using testosterone and DHEA in women for most conditions due to safety and effectiveness concerns, but suggest considering testosterone for postmenopausal women with low sexual desire.

Testosterone replacement may help some postmenopausal women with symptoms like fatigue and low libido, but more research is needed to fully understand its effects.

Testosterone therapy seems safe for postmenopausal women for a few years, but more research is needed for long-term effects.

Androgens play a role in female sexual function, and testosterone therapy can help women with low sexual desire, but more research is needed on treatments and long-term safety.

The review recommends hormone replacement therapy for women with premature ovarian insufficiency to manage symptoms and protect health, with specific approaches for different groups.

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

Some medications can cause acne, and stopping these drugs is the main treatment.

Testosterone replacement may improve sexual desire and bone health in women with low androgen levels, but more research is needed on its long-term safety.

Short-term testosterone therapy in women seems safe with few mild side effects, but long-term effects need more research.

Testosterone therapy can help improve sexual desire and function in postmenopausal women but may cause side effects and is not FDA-approved for this use.