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miR-203a-3p helps hair follicle stem cells become specialized by targeting Smad1.

A three-year-old girl survived a rare serious infection caused by BCG vaccination, which improved after treatment with a leprosy drug.

The LEF-1 gene in cashmere goats was successfully cloned and analyzed, showing potential for improving cashmere production.

The treatment improved prostate health in mice.

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A boronic acid copolymer quickly forms cell clusters, useful for tissue and tumor modeling.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Ginkgolide B and bilobalide help mink hair grow by making skin cells healthier and boosting a key growth protein.

Finasteride treatment increased blood volume and reduced vessel leakiness in beagle prostates.

The hair tonic with cinnamon oil and coconut oil was stable and caused very mild irritation.

MCPIP1 in myeloid cells is important for skin cancer development and healthy hair growth.

Alkaline Ceramidase 1 prevents early hair loss in mice by keeping hair follicle stem cells balanced.

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Scientists made two new chemicals that might help treat diseases caused by male hormones.

FLCN helps control iron levels in cells.

Corneal health relies on cell migration and cooperation with the lacrimal gland, not Bmi1+ cells, and Eda gene mutations can cause dry eye disease.

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A small group of slow-growing cells causes basal cell carcinoma to return after treatment.

Carbamazepine caused hair loss in a man, which stopped after he stopped taking the drug.

Certain plant compounds can help prevent and treat a virus in pigs.

The man's rash, hair loss, and vision issues were due to syphilis, not CMV.

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A mother and her two daughters got a skin infection from their cat.

CCCA causes progressive hair loss in Black women, starting from a central scalp patch.

pbn-STAC effectively finds strategies for cellular reprogramming using deep reinforcement learning.

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The new near-infrared LED device improves skin and hair with no side effects.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.