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Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

A family had a genetic condition causing hair loss on the scalp, passed down through four generations.

A specific gene change in APCDD1 increases the risk of hair loss.

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

HAP stem cells in hair follicles could help repair nerves and spinal cords.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

A specific gene mutation causes congenital hair loss.

Minoxidil boosts hair growth by increasing blood flow and nutrients to hair follicles.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

HLA can be linked to autoimmune hepatitis.

KAP genes are crucial for hair development and show both shared and unique traits in humans, chimpanzees, and baboons.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

The hair keratin variant is mostly found in Caucasians.

A specific gene variant may increase the risk of developing Alopecia Areata.

Two new gene clusters important for hair formation were found on human chromosome 11.

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

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

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

Two new gene clusters important for hair formation were found on human chromosome 11.

New mutations in the hairless gene may cause hair loss and affect bone development.

CT60 polymorphism might increase the risk of Alopecia Areata.

A mutation in the human hairless gene causes alopecia universalis.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.