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The medication combination did not affect glucose tolerance but increased some cholesterol levels due to its estrogen component.

Flutamide combined with an LHRH agonist effectively inhibits prostate growth, suggesting it could treat prostate cancer.

The document suggests that targeting the hormone DHT could be a more effective treatment for prostate cancer than targeting testosterone.

Finasteride effectively lowers specific hormone levels, helping monitor treatment progress.

The document concludes that accurate measurement of serum androgens is crucial for diagnosing hyperandrogenism.

The androgen receptor is a promising target for breast cancer treatment, especially in triple-negative cases, but more research is needed for personalized therapies.

LY191704 is a compound that effectively blocks a specific enzyme involved in hormone conversion and could help treat enlarged prostate and hair loss.

Finasteride slowly binds to 5-alpha-reductase, affecting enzyme stability and inhibitor potency.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

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.

Finasteride treats hair loss but may cause low libido, erectile issues, and depression.

Finasteride may cause lasting sexual, mental, and physical symptoms; use with caution.

Male pattern baldness may be caused by factors like poor blood circulation, scalp tension, stress, and hormonal imbalances, but the exact causes are still unclear.

Using photoacoustic waves to deliver minoxidil improves hair growth effectively and safely.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Bolandiol, a synthetic steroid, builds muscle and bone without greatly affecting sex glands, and works differently from other hormones.

Lipid nanoparticles can help deliver drugs through hair follicles but struggle to penetrate deeper skin layers.

Finasteride's sexual side effects not caused by androgen deficiency or SRD5A inhibition.

5α reductase inhibitors treat hair loss but may cause sexual side effects and risks.

Androgens, male hormones, affect physical and mental functions, with a decrease leading to health issues like muscle loss, bone disease, and depression, and more research is needed on long-term effects and treatments.

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

New treatments for low male hormones improved sexual function and mood but had unclear risks, especially for older men.

Rat skin takes up and processes testosterone differently than other organs, with testosterone being more important for the skin than its metabolite 5α-DHT.

Metabolite 7 is a strong inhibitor for Alzheimer's disease management.

The conclusion is that tritium-labeled testosterone metabolites can be made and are better converted into dihydrotestosterone in skin cells than in prostate tissue.

Creating stronger blockers for skin enzymes might lead to better treatment for conditions like acne and excessive hair growth.

The enzyme sEH is important for hair growth and its inhibition could help treat hair loss.

Certain 4-azasteroids are effective at blocking the enzyme that processes testosterone in human skin and could help treat acne, excessive hair growth, and male pattern baldness.

Hair regrowth slows with age and can be affected by treatments that change enzyme activity in the skin.

Finasteride reduces alcohol withdrawal severity in male mice but increases it in female mice.