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Farudodstat may help prevent hair loss in alopecia areata by stopping immune attacks on hair follicles.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

Syphilis patients showed abnormal hair root changes, with no difference between primary and secondary stages.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

CD4 T cells need IFN-γ to cause hair loss in alopecia areata.

Genetic testing can diagnose hair loss linked to DSG4 gene variants.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

IL16 gene variations may affect the risk of alopecia areata in Koreans.

A 12-year-old boy had severe shingles and skin damage after a stem-cell transplant.

Trichohyalin in hair can trigger immune attacks in alopecia areata.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

The skin of both rat strains showed similar lectin binding patterns.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

Genetic marker rs12558842 strongly linked to male hair loss.

A truncated protein linked to breast cancer may change cell adhesion.

IL-15 helps protect hair follicles from immune attacks and encourages hair growth.

A new gene mutation is linked to monilethrix in the studied family.

A gene mutation causes monilethrix in a Chinese family.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Human hair contains a substance that shows blood group A activity.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.