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Ritlecitinib improves emotional well-being and activity levels in alopecia areata patients.

Two new gene mutations cause a rare hair disorder.

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

A new patch can deliver stable antibodies over time for potential HIV treatment.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

The enzyme Rand protease works well for leather dehairing and its stability is important, with Leu75 playing a key role.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

SRD5A2 methylation in blood can predict how well someone will respond to finasteride treatment.

A mutant FERONIA gene affects root hair growth at high temperatures.

RORA plays a key role in controlling seasonal hair molting by affecting hair follicle cell activity.

The IRF2BP2 gene affects sheep fleece quality by influencing fiber traits.

Methylation of the 5-AR2 gene may cause resistance to Finasteride in BPH patients.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.

A gene mutation causes curly hair and hair loss in rats.

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Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

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A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.