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Many treatments for hair loss lack proper testing and FDA approval, so their effectiveness is uncertain.

Two people lost hair unexpectedly after getting a common hair loss treatment with a drug called Dutasteride.

Finasteride's effectiveness for frontal fibrosing alopecia is uncertain.

The mouse model suggests male pattern baldness may be due to an enzyme increasing DHT and higher androgen receptor levels in hair follicles.

Hormones and neuropeptides affect hair growth, with androgens having opposite effects on beard and scalp hair.

Finasteride reduces hair growth in women with hirsutism and works better with electrolysis.

Nepenthes kampotiana extract can potentially prevent hair loss and could be an effective treatment for common baldness.

The lotion with specific plant extracts effectively increased hair growth and improved hair cycle in subjects after 3 months.

Androgenetic alopecia involves genetics, hormones, and can be treated with medications or surgery.

DHT reduces a cell's ability to promote hair growth, while 3D culture without DHT improves it.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Blocking the enzyme 5α-reductase can shrink the prostate and help treat enlarged prostate issues.

Finasteride poorly inhibits type 1 5AR, affecting its effectiveness.

The higher dose supplement was more effective in treating female hair loss.

Wnt-10b is important for keeping mouse skin cells healthy for hair growth.

Researchers developed a model to predict how well certain compounds can block an enzyme related to hair loss and prostate issues, suggesting a 50 mg dose of finasteride might be effective based on lab and body data.

New compounds may help treat prostate cancer by reducing cell growth.

Finasteride is effective in growing hair and stopping hair loss in men with mild to moderate alopecia.

Male pattern baldness is caused by certain cells in hair follicles and could potentially be treated by targeting a specific growth factor, TGF-β1.

Dutasteride and finasteride do not significantly affect bone density, blood fats, or blood production, but slightly lower PSA levels and minimally impact sexual function in healthy young men.

Substances from human hair cells can affect hair loss-related genes, potentially leading to new treatments for baldness.

Taking 5α-reductase inhibitors with prednisolone can worsen its negative effects on metabolism.

Men with lower education levels are more likely to have erectile dysfunction if they have coronary artery disease.

Finasteride reduces hair loss and treats BPH without major hormone changes, but may cause sexual dysfunction.

People with hair loss have more androgen receptors and enzymes in certain follicles, with men and women showing different patterns.

5α-reductase is essential for male sexual development and its inhibitors have potential in treating various conditions related to hormone action.

Enzymes called 5α-reductases have many body functions and need more research to safely use inhibitors.

We need to learn more about 5α-reductases and neuroactive steroids to safely make drugs targeting these enzymes.

Enz_MoriL from mulberry leaves helps hair growth by affecting specific cell pathways.