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LHX2 and SOX9 identify unique hair follicle cell groups, crucial for hair maintenance.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

A new type of nerve cell involved in itch perception was discovered.

Sox9 levels in brain stem cells affect whether they stay as stem cells or become neurons.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

BST2 is highly expressed in certain immune cells in alopecia areata, suggesting a role in the disease.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Mutations in Far2 mice cause hair loss due to sebaceous gland issues.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.