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Alpha-difluoromethylornithine prevents cancer in mice but causes hair loss.

A 27-year-old with APS-1 showed improvement in symptoms after treatment.

FOXN1 duplication can cause excessive hair growth.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

The nutritional supplement Pilopeptan® WOMAN improved hair growth and thickness in women with hair loss.

A new compound, HTPI, promotes hair growth by protecting cells from damage and regulating energy use.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Mutations in the HOXC13 gene cause hair and nail development issues.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

Increased PHGDH expression causes early melanin buildup in hair follicles.

A rare, harmless hair condition was found in an infant's eyebrow, needing no treatment.

The study found that pili bifurcati causes hair to intermittently split into two branches, each with its own outer layer.

A peptide from hair follicle stem cells promotes hair growth by activating specific skin cells.

PTHrP is important for bone formation and may be targeted for osteoporosis treatment and longevity therapies.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

A genetic mutation in the LIPH gene causes hair loss and growth defects.

Certain peptides can prevent hair loss in young rats caused by a cancer drug.

IL-1β inhibits human hair follicle growth.

The TIP1 gene is crucial for normal plant cell growth in Arabidopsis.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

A new therapy for a skin blistering condition has not been developed yet.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

Enzyme replacement therapy may help alleviate symptoms in complex cases like this.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

A new type of pachyonychia congenita may exist, caused by a different keratin mutation.

The hr gene is linked to hair loss in Valle del Belice sheep.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

The Cyp11a1 gene variation has a weak link to PCOS, but higher di-hydro-testosterone levels are found in PCOS patients.