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Changing estrogen levels during menopause might affect genes related to body rhythms and cause increased hair loss.

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

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.

A mutation in the IL2RA gene increases the risk of 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.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.

Wnt genes help starfish regrow arms by aiding wound healing and cell development.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Deleting the Sox21 gene changes hair lipid composition and increases cholesterol sulfate levels.

Mutation in hairless gene may increase hair loss risk.

Staphylococcus aureus delays wound healing by disrupting lipid metabolism in skin cells.

Mutating the gmds gene in zebrafish increases hair cell numbers and regeneration.

Certain gene variations are linked to alopecia areata.

Four genes affect hair follicle density in goats.

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

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

The SOSTDC1 gene is crucial for determining sheep wool type.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Certain genes may help Bulgarians live longer.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

A new technology showed that the SOX9 gene might control heart scar formation after injury, suggesting new treatment possibilities.

A new gene mutation causes complete androgen insensitivity in a 16-year-old with a female appearance.

The study found genetic diversity in coat color dilution among Czech pointers in Slovakia.

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