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A substance from Caulerpa racemosa seaweed may protect against skin damage caused by air pollution by reducing oxidative stress and cell death.

Letrozole reduces seizures but not brain damage in mice.

MT-DADMe-ImmA can selectively kill head and neck cancer cells without harming normal cells.

A wearable cap-like device using light therapy reduced scalp skin lesions by 71% and was painless.

Finasteride reduces alcohol consumption in mice by affecting brain chemicals.

Calanthoside, a potential hair growth stimulant, was successfully synthesized using a new, efficient method.

Drinking kava tea can cause a skin reaction with red, swollen bumps, which may improve with steroids.

Disrupted citric acid metabolism stops hair growth.

Deoxycholic acid effectively reduces double chin fat with temporary side effects and high patient satisfaction.

Valproic acid can cause dark lines on nails.

The May issue discussed publishing agreements and four studies on cholesterol in hair, cancer cell changes, hormones in the uterus, and skin protein effects.

1′S-1′-Acetoxychavicol acetate may help treat hair loss by reducing oxidative stress.

m⁶A methylation is crucial for proper wound healing and tissue repair.

Melanogenesis inhibitors like kojic acid and niacinamide can reduce inflammation and pigment production in skin cells.

Inclisiran is effective at lowering cholesterol.

Kojyl cinnamate ester derivatives can promote hair growth by increasing adiponectin production in fat tissues.

Copper and iron cause keratin damage in hair by converting methionine to homocysteine.

Potassium channel openers are effective in treating heart conditions, high blood pressure, pulmonary diseases, bladder issues, and hair loss, but more selective drugs are needed.

Targeting lipid metabolism can help treat advanced, resistant cancers.

The modified oriental prescriptions help hair growth and melanin production without irritating the skin.

Heavy metals can damage skin and hair in mice.

Certain compounds reduced hamster flank organ size by inhibiting 5α-reductase, like finasteride, without affecting androgen receptors.

Methylation in specific gene region causes finasteride resistance in some BPH patients.