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The FTO gene hinders stem cells in hair follicles from becoming pigment cells.

Black hairs have more pigment-related genes, while gray hairs have more keratin-related genes.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

The method safely and efficiently delivers genes to the skin but may not work for conditions needing high levels of gene products.

HT-scCAT-seq helps understand gene regulation in embryonic skin development.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

A 195 bp duplication in the HOXC10 gene causes crests in domestic chickens.

A specific gene mutation causes congenital hair loss.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

A gene called HDAC9 might be a new factor in male-pattern baldness.

61 functional keratin genes were identified in dogs and horses, leading to updated gene annotations.

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Mice with human gene experienced hair loss when treated with DHT.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Researchers found specific genes in the part of hair follicles that could help treat hair disorders.

Wnt signaling helps regenerate hair follicles in wounds by reducing skin cell sensitivity to mechanical stress.

Genes linked to wool fineness in sheep have been identified.

Gene linked to common hair loss found, may lead to new treatments.

The Hairless gene is crucial for healthy skin and hair growth.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

A new gene mutation linked to a skin condition was found in a Spanish family.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Increased PHGDH expression causes early melanin buildup in hair follicles.

Gene therapy, especially using atoh1, shows promise for creating functional sensory hair cells in the inner ear, but dosing and side effects need to be managed for clinical application.