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A new method effectively predicts estrogen-related health effects for early screening.

The study aims to create a model to predict health attributes using diverse health data from Japanese adults.

UHP-sCESr is as effective as HESr for treating BPH symptoms.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A mutation in mice causes hair loss and immune problems.

Hair follicle stem cells can become heart muscle cells.

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Baicapil was effective in reducing hair loss and increasing hair growth in women with telogen effluvium.

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

Early intervention and protective measures are crucial for managing CIPA due to the lack of pain and standard treatment.

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Baricitinib treatment can help regrow scalp hair and eyebrows or eyelashes in people with severe alopecia areata.

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Hoxc13 is essential for hair growth and follicle development.

Diphenylcyclopropenone treatment helps hair growth in alopecia areata by promoting blood vessel growth and cell survival.

Black women with CCCA are more likely to have uterine fibroids.

CCCA can occur in children and needs early diagnosis to prevent permanent hair loss.

Topical immunotherapy with DPCP led to some hair regrowth in most pediatric alopecia areata patients, especially those with milder cases and longer treatment.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Knockout mice showed anemia and hair loss, suggesting other ways exist for iron absorption.

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Melatonin affects when and how goat hair follicle genes turn on and off during growth cycles.

Diphenylcyclopropenone treatment helps prevent hair loss relapse in alopecia areata patients.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

Diphencyprone increases Bcl-2 protein in patients with hair regrowth from alopecia areata.

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Cicatricial pattern hair loss is likely advanced common baldness, not a type of lichen planopilaris.

New mutations in the hairless gene may cause hair loss and affect bone development.

IL-17C is important in inflammatory skin diseases and could be a target for treatment.