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The investigation found no work-related causes for employee hair loss at Equifax Payment Services, and the environment was not hazardous.

The study created a new model to better understand human hair growth and health.

Cathepsin L deficiency causes hair and skin issues in mice.

Multicomponent crystals in microneedles improve drug delivery for hair loss treatment.

Antiandrogen therapy may help treat hidradenitis suppurativa.

The updated NPRT system now covers different types of hair loss in men and women.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

4-O-Methylhonokiol helps protect skin cells from growth-stopping effects of a protein by regulating growth-related pathways.

Vδ1+ T-cells in the skin contribute to hair loss in alopecia areata and could be targeted for treatment.

Nonimmunogenic forms of keratins K71 and K31 can delay and prevent alopecia areata.

A specific RNA increases hair stem cell growth and skin healing by affecting a protein through interaction with a microRNA.

Hippocampus sparing whole brain radiation therapy prevents hair loss and preserves cognitive function.

Certain CD8+ T cells attack hair follicles in alopecia areata, suggesting they could be targeted for treatment.

Laser hair removal effectively reduces hidradenitis suppurativa symptoms with few side effects.

Microneedles offer a painless, effective, and easy-to-use hair loss treatment.

EZH1 and EZH2 are crucial for healthy hair growth and skin repair.

Keratin films from human hair can potentially replace human nail plates for drug testing.

Korean medicinal herbs in hair tonic and food increased hair growth in mice.

HDAC6 helps keep ovarian follicles dormant, extending female fertility.

Estrogen and MLL enzymes work together to regulate genes important for hair growth and leukemia.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

ALRN-6924 may prevent hair loss caused by chemotherapy.

The study aims to create a model to improve personalized and preventive health care.

An 8-year-old boy with Recklinghausen's Disease shows various symptoms and is from a family with close genetic ties.

HDMHG0401-10 treatment significantly improved hair count and was better than a placebo in reducing hair loss in men with hereditary hair loss, with no major side effects.

Certain genes may influence hair loss differently in men and women.

A 13-year-old boy with a rare genetic condition survived a heart attack and improved with treatment.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.