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Hidradenitis suppurativa is a chronic skin condition more common in women, linked to genetics and lifestyle factors, and associated with various other health issues.

Mutations in the LIPH gene cause woolly hair in a child.

Hair follicle stem cells can become heart muscle cells.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Liposomal IGF-1 safely and effectively treats hair loss in hamsters.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

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A specific chemical change in the S100A3 protein leads to the formation of a four-part structure important for hair formation.

Hyaluronan is a good drug delivery material because it sticks to mucosal areas and its drug release can be improved by changing its properties.

The skin of both rat strains showed similar lectin binding patterns.

Tanshinone IIA helps protect skin tissue from low oxygen damage by boosting certain cell markers.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

HPDAlR nanoparticles greatly improve skin wound healing without toxicity.

THA is a rare condition with no significant clinical consequences if thyroid function is normal.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

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

Hair follicle stem cells work well with bladder matrix for bladder repair.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Hormones might affect the skin condition hidradenitis suppurativa, but their exact role is unclear.

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

Human hair keratin helps regenerate rat sciatic nerves by transforming Schwann cells and protecting axons.

The transporter protein SH1446 in Staphylococcus hominis is key to underarm odor production.

Overexpression of the HE4 gene in mice causes eye inflammation and cloudiness.

CAP1/Prss8 does not activate PAR2 or inhibit PN-1.

A gene deletion in DSG4 causes sparse hair in some Pakistani families.