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A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Keratin mutations may cause scarring alopecia by damaging hair structure.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

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

Two specific genetic markers increase the risk of hair loss in Asian populations.

MCHR2 gene duplications may be linked to alopecia areata.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

Using special RNA to target a mutant gene fixed hair problems in mice.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

The study found that the protein Dkk4 helps regulate hair growth by controlling Wnt signaling in mice.

LSD1 is essential for healthy skin development and creating the skin's protective barrier.

Alk1 in specific cells is crucial for proper nerve branching and hair function.

H3K4me3 helps control RSPO3 to influence hair growth and development.

PCAT1 helps hair growth by controlling miR-329/Wnt10b.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Activating cannabinoid receptor 1 reduces certain keratin levels, potentially aiding psoriasis treatment.

Keratin 79 cells help form and regenerate hair canals.

MED1 is essential for normal hair growth and maintaining hair follicle stem cells.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

Basonuclin helps keratinocytes multiply and prevents them from fully maturing.

Loss of Ten1 in mice causes telomere shortening and symptoms similar to human dyskeratosis congenita.

Major histocompatibility antigens are found in specific skin cells and structures, but not in sweat glands.

Rac1 is vital for hair follicle health but not needed for skin maintenance.

Scientists created a detailed map of gene activity in different parts of human hair follicles.