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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Cyclohexyl salicylate promotes human hair growth and increases certain hair follicle stem cell progeny.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

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The guideline recommends using specific drugs and surgery together for treating hidradenitis suppurativa effectively.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

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Higher hair luminosity and shine mean higher perceived transparency.

The Greek DCQ is a reliable and valid tool for assessing dysmorphic concern.

SKH1 hairless mice have identifiable epidermal stem cells with specific markers.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

Researchers created a new mouse model for studying scleroderma.

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A new mutation in the ST14 gene was found in a patient with ARIH syndrome, showing milder symptoms and no tooth issues.

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Selenium disulfide shampoo effectively reduces dandruff and is well-liked by users.

Older men's scalp damage increases with age and sun exposure, a baby girl in the Philippines has Schimmelpenning syndrome, and thyroid screening is advised for children with hair loss and certain risk factors.

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Mice hair follicles take in the amino acid cystine.

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TRIV-509 quickly improves skin barrier and cell health in atopic dermatitis.

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A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.