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Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

A 72-year-old man was diagnosed with a rare skin form of Rosai-Dorfman disease after years of misdiagnosis.

A nonviral method was developed to label and culture human hair follicle stem cells.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

Keratoacanthoma changes as it grows, showing different hair follicle characteristics at each stage.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

K6hf is a unique protein found only in a specific layer of hair follicles.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

Hair follicle bumps with stem cells might contribute to permanent hair loss by getting disconnected due to scarring.