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A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

Topical DHEA safely increases skin oil production.

Four new compounds were more effective than finasteride in treating prostate issues and hair loss, with one being 100 times more active and safe for use.

Lipase H is important for hair follicle function and shaping hair fibers.

Hibiscus rosa sinensis may help manage hair loss.

Sulfotransferase SULT1A1 activity may predict minoxidil treatment success for hair loss.

Epristeride's metabolism involves key metabolites and proteins, affecting its use in doping tests.

A specific gene mutation causes monilethrix in this family, and minoxidil treatment improves hair condition.

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.

Tea tree oil is more effective for treating human demodicosis than other treatments.

PMEE may help reverse greying hair by boosting melanin production.

Finasteride reduces prostate size and DHT in male mastomys but not in females.

Retinoic acid and DMSO improve gene delivery to mouse skin for potential hair and skin disease treatment.

Increased PHGDH expression causes early melanin buildup in hair follicles.

Melatonin directly affects mouse hair follicles and may influence hair growth.

Excessive putrescine causes hair loss in transgenic mice by disrupting hair follicle development.

The method accurately measures testosterone metabolites with high sensitivity and low environmental impact.

Reducing miR-30a-5p helps hair follicle stem cells grow and survive.

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

A new test more accurately detects citrulline in hair follicles and pilomatrixomas.

Modified pep7, named EPM peptide, effectively promotes hair growth at low concentrations and works well with minoxidil.

A new method was created to test the effectiveness of Dihydrotestosterone (DHT) inhibitors, like finasteride and dutasteride, in human and fish cells. The results showed fish cells are more sensitive to these treatments, and dutasteride works better than finasteride in all tested cells.

Synthetic hormone treatment reduces melanin and hair growth in rats.

Testosterone affects androgen receptors and lipid storage in cells, while DHEA does not convert to testosterone or affect these receptors in the same way.

The more lipophilic the progesterone derivative, the better it binds to androgen receptors and has antiandrogenic effects.

Finasteride's metabolites were identified, helping understand how the drug is processed in the body.

DHEA reduction may be linked to frontal fibrosing alopecia, but more research is needed.

Higher SRD5A2 expression predicts better response to finasteride in treating urinary symptoms.