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A compound from brown algae boosts the production of a certain inflammatory substance in skin cells.

The two finasteride formulations are bioequivalent.

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

Psychotropic drugs can interact with natural products, affecting their effectiveness and safety.

Cuscuta reflexa extracts helped regrow hair in rats with drug-induced hair loss.

Isotretinoin is recommended for acne treatment as it is as effective as cyproterone compound.

Certain inhibitors can potentially treat prostate cancer and other hormone-dependent conditions by controlling sex hormone levels in cells.

Cubosomal gels enhance skin absorption of cetirizine better than niosomal gels.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

Genetic variations may affect how well finasteride works for BPH patients.

New treatments for Hepatitis C show promise but need more research to confirm their safety and effectiveness for clinical use.

A cystic fibrosis patient developed Cushing's syndrome from a drug interaction between itraconazole and budesonide, which improved after stopping the medications.

FCE 28260 is a stronger and longer-lasting inhibitor of 5α-reductase than finasteride, which may make it a better treatment for certain medical conditions.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

High doses of cyproterone acetate increase the risk of brain tumors in women, but the risk decreases after stopping the medication.

Type 3 5α-reductase is more common and finasteride and dutasteride strongly inhibit it.

Compound 7p shows strong potential as an anticancer agent.

Cytarabine can cause multiple organ toxicities, especially neurotoxicity, but better research methods are needed to fully understand and predict these effects.

A brominated phenoxy compound effectively inhibits a human enzyme and shows potential for clinical use.

Three specific 4-azasteroid-2-oximes showed strong enzyme inhibition, but less than finasteride.

A specific protein complex increases the activity of a plant enzyme, but this action is not required for plant root hair growth.

Smaller particles of the drug carrier penetrated skin better, with 300 nm size being best for targeting hair follicles.

2-Hydroxy-1,4-naphthoquinone is a strong 5α-reductase inhibitor.

Domestic and imported finasteride tablets are bioequivalent.

Clobetasol nanocarriers can be effectively delivered to hair follicles, with uptake improved by massage and affected by particle type.

Steroidogenesis inhibitors change but don't stop androgen production in prostate cancer.