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Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.

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Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.

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Using a teletriage system greatly increased access to skin care for uninsured Latino immigrants at a clinic.

Li2CO3 improved skin disease in a mouse model of Focal Dermal Hypoplasia without toxicity.

Zinc supplements improved symptoms in a Uyghur infant with a rare genetic disorder affecting zinc absorption.

Clinical trials for hair loss in the USA show differences in participation among different races and ethnic groups.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

ATR04-484 ointment shows promise for treating skin issues from cancer therapies.

Four keratin genes are crucial for hair growth in Xinji fine wool sheep.

Genetic testing is crucial for diagnosing and managing non-Herlitz junctional epidermolysis bullosa.

The prototype for analyzing skin aging works technically and clinically.

The protocol allows easy imaging of dividing cells in C. elegans and can be used for other organisms.

ISCK03 stops melanin production in human melanoma cells and lightens skin color in mice and guinea pigs.

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