Search

everythinglearnresearchcommunity

for

Search:↓

Blocking the androgen receptor in skin cells reduces their growth response to male hormones, suggesting a possible treatment for skin conditions linked to androgens.

Sex neurosteroids cause different effects on hippocampal synaptic plasticity in males and females.

Finasteride does not prevent bladder cancer.

The plant extracts may help treat hair loss by promoting hair growth and reducing DHT levels.

The rat model showed early perimenopause with regular cycles and low hormones, and late perimenopause with irregular cycles and higher hormone levels.

Plant-based compounds might be a promising alternative for prostate cancer treatment with fewer side effects.

Finasteride changes hormone levels and certain proteins in rats, but these effects can be reversed after stopping the drug.

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.

Saw palmetto extract can block the enzyme that converts testosterone in pig prostate cells.

The enzyme type 1 5α-reductase is more active in the hair follicle's lower part than in the skin's outer layer.

New compounds were made that effectively block enzymes related to prostate issues and hair loss.

Green algae can break down finasteride, reducing environmental harm.

Diane 35 plus finasteride is more effective in reducing hair growth and androgen levels, but may decrease libido.

SHBG binding properties are unchanged in male liver cirrhosis patients.

Accurate method measures finasteride levels in human plasma using gas chromatography-mass spectrometry.

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.

Testosterone therapy is beneficial for women's health and does not cause masculinization or liver damage, and it protects the heart and breasts.

Some hormone-related drugs may protect brain cells in Parkinson's disease differently in men and women.

Finasteride and minoxidil are effective FDA-approved treatments for androgenetic alopecia.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

Researchers found new potential but less potent rat enzyme inhibitors using a 3D model.

Post-finasteride syndrome causes lasting sexual, neurological, and physical side effects in some people after taking finasteride.

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.

Skin changes can indicate hormonal imbalances and help diagnose endocrine disorders.

Finasteride increases hair growth, prolongs hair cycle, and lowers dihydrotestosterone levels.

Finasteride changes antioxidant enzyme expression, possibly affecting sperm protection in rats.

Scientists made new substances that can block an enzyme linked to prostate issues and hair loss, with potential for creating a new treatment.

Early diagnosis and treatment, using finasteride, minoxidil, or hair transplantation, improves hair loss outcomes.

The conclusion is that managing androgen excess requires long-term treatment, including hormonal contraceptives and androgen blockers, with follow-up after six months.

Finasteride reduces hairiness and androgen levels in women with unexplained excessive hair growth.