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A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

SA linked to mitochondrial issues and oxidative stress, while AGA involves disrupted hair growth genes.

A mutation in the Sgkl gene causes defective hair growth in mice.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

A new gene causes hairlessness and skin cysts in rats.

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

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

ESR2 gene linked to female-pattern hair loss.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21, near the hairless gene.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

Certain gene changes in osteopontin are linked to higher risk of atopic dermatitis and asthma.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

The PLP2 gene affects cashmere fiber quality in goats and is linked to hair growth and loss.

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

Guasha changed rat skin appearance and blood vessels temporarily without affecting certain nerve proteins or fiber structure.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

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

A new mutation in the KRT86 gene causes monilethrix in a Han family.

TBX5 gene influences feathered feet in Guangxi chickens by affecting cell growth and movement.

m6A-circHECA may affect cashmere goat hair growth and is possibly controlled by gene promoter methylation.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

The WIF1 gene is crucial for hair growth in Angora rabbits.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Certain gene variants are linked to a higher risk of polycystic ovary syndrome, hair loss, and obesity in women from western Saudi Arabia.