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A woman's progressive hair loss was correctly diagnosed as a rare condition called fibrosing alopecia in a pattern distribution after initially being mistaken for a more common type.

The document reports the first case of a rare skin condition in Colombia, the 19th case worldwide.

Combining ficlatuzumab and gefitinib can cause severe scarring hair loss.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

The PP2A-B55α protein is essential for brain and skin development in embryos.

The conclusion is that understanding how hair follicle stem cells live or die is important for maintaining healthy tissue and repairing injuries, and could help treat hair loss, but there are still challenges to overcome.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.

Mice without the Sept4/ARTS gene heal wounds better due to more stem cells that don't die easily.

High levels of the protein Flightless I worsen ulcerative colitis symptoms in mice.