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Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

The compounds tested could potentially treat hair loss and alopecia.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

A 65-year-old man developed a serious skin cancer linked to a drug he was taking for a fungal infection after a bone marrow transplant.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

The GG genotype of the KRT71 gene leads to longer wool in Gansu alpine fine-wool sheep.

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Ritlecitinib is safe and well-tolerated for treating alopecia areata in patients aged 12 and older.

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rwSALT accurately measures hair regrowth in alopecia areata using scalp photos.

KLHL24-mutant stem cells help understand skin and heart disease.

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A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

LLPS is crucial for RALF signaling, aiding plant growth and stress resilience.

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