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The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

A girl had two rare hair conditions that helped understand their overlap.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

The HDDPiW-jSB solution may prevent hair loss caused by docetaxel in rats when applied regularly.

A new group called the Asian Association of Hair Restoration Surgeons (AAHRS) has been created.

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Adult somatic stem cells could be used for future skin therapies.

JAK/STAT1 pathway causes hair loss during chemotherapy by reducing Shh in hair follicles.

Scientists found a gene in mice that causes early hearing loss.

The American Society of Hair Restoration Surgery (ASHRS) is a group focused on improving hair restoration methods.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

People with Down syndrome often have skin issues and need regular check-ups for early treatment.

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Deuruxolitinib effectively regrows hair in adults with alopecia areata and is well tolerated.

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New medications could improve treatment for severe alopecia areata in Australia.

Topical JAK inhibitors may help children with alopecia areata regrow hair.

MSM supplementation in kittens improves hair quality and growth rate without harming their health.

JAK/STAT inhibitors show promise for skin diseases but aren't yet approved.

JAK inhibitors can effectively reverse hair loss in people with alopecia areata.

Wharton's jelly stem cells show diverse traits and functions.