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Alopecia areata patients show increased inflammation and OX40 activation, suggesting a new treatment target.

Blocking BACE1 and BACE2 enzymes causes hair color loss in mice.

Blocking certain immune signals can reduce skin damage from radiation therapy.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

A specific gene mutation causes a severe skin disorder in a family.

Stat3 activation increases hair follicle progenitors but reduces bulge region stem cells.

Activated erbB-2 in mice skin causes severe skin and hair abnormalities.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

A new technology showed that the SOX9 gene might control heart scar formation after injury, suggesting new treatment possibilities.

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