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A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

FLCN helps control iron levels in cells.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

Using human recombinant hyaluronidase in donor strip harvesting may improve the procedure.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

The LMNA mutation affects skin structure even in asymptomatic carriers.

Cronkhite-Canada syndrome is rare, with high mortality and cancer risk, needing more research for treatment guidelines.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

Mutations in the hairless protein gene cause hair loss.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

Too much keratin 16 in mice skin causes abnormal skin thickening and structure.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

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

A certain genetic variant in the androgen receptor may predict the severity of COVID-19 in men.

rRSPO1 protein boosts hair growth by activating a key signaling pathway.

A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

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

A stable, active version of a growth factor was made in bacteria, showing promise for medical use.

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

K6hf is a unique protein found only in a specific layer of hair follicles.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

Human anagen hair follicles have unique carbohydrate patterns during keratinization.

Gene variation affects prostate issues and hair loss.

Hair sensitivity to androgens is partly controlled by specific enzyme expressions in different hair areas.

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.