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

A mutation in mice causes hair loss and immune problems.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

HLD10 can include increased body hair and Mongolian spots.

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.

Several genes, including Hox-7A, Stra6, and Lim-1, are involved in normal palate formation.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

LGR5 is a common marker of hair follicle stem cells in different animals and is important for hair growth and regeneration.

Mutations in the hairless gene cause a rare form of permanent hair loss.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

HB24 helps convert IBA to IAA, promoting root hair growth.

The research identified a gene in sheep important for wool quality, which could help improve wool traits.

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

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

A feedback loop between LRH and RSL4 controls root hair growth in Arabidopsis.

A mutation in the KRT82 gene is significantly associated with Alopecia Areata.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

The SbbHLH85 protein helps sweet sorghum grow more root hairs but makes the plant more sensitive to salt.

SLC24A5 shows a clear selective sweep, but no link to UV radiation intensity.

Mutations in the HOXC13 gene cause hair and nail development issues.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

CLK1 is needed for skin cells to become epidermal cells but not sebocytes.

New genetic mutations causing hair loss were found in a Chinese family.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.