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A new method accurately measures molecular movement without complex modeling.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Curly wool has more orthocortex than straight wool.

A 6-year-old girl was diagnosed with a rare hair disorder called monilethrix.

A woman had a non-cancerous skin tumor on her eyelid removed successfully.

Different parts of the nail express different keratins, showing unique patterns of differentiation.

Keratoacanthoma and some squamous cell carcinomas are linked to hair follicles, while others are not.

A 6-year-old girl had both monilethrix and trichorrhexis nodosa, causing brittle hair, with minimal improvement from treatment.

Steroid treatment improved both gut and nerve symptoms in a man with Cronkhite–Canada syndrome.

Ketoconazole's structure and dynamics are linked, aiding antifungal drug development.

Monilethrix is a rare, inherited condition causing fragile hair and hair loss, with no cure but some treatments may help.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

Matrical tumors share a common growth mechanism involving the Wnt pathway and consistent PHLDA1 expression.

A 4-year-old boy has a rare type of hair loss in a line pattern on his scalp.

A baby girl's hair turned straight on one side due to a neck tumor and surgery, but it returned to curly as she recovered.

Acitretin improved monilethrix symptoms temporarily, but they returned after stopping treatment.

The family has a unique form of ectodermal dysplasia similar to Clouston syndrome but with different hair and skin symptoms.

A man had a non-cancerous, fast-growing skin lump on his arm that was removed with surgery.

A painless cheek lump was misdiagnosed but later identified as a rare benign skin lesion called pilomatrixoma.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Keratinous tissues have multiple structural layers, including ordered keratin and lipid granules.

A new DSG4 gene mutation causes hair defects in a young girl.

Hair changes and a high occipital hairline may help diagnose Trichorhinophalangeal Syndrome.