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Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

Dlx3 is essential for hair growth and regeneration.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

PRX01, PRX44, and PRX73 are essential for root hair growth in Arabidopsis thaliana.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

Baicalin may help reduce excessive male hormone levels in PCOS.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

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

Caffeine can damage hearing cells and affect hearing recovery after ear trauma.

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

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.

Removing the VDR gene in skin cells reduces their growth and affects hair-related genes.

A gene mutation in Lama3 is linked to a common type of hair loss.

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

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

The study identified unique genes in hair follicle cells and their environment, suggesting these genes help organize cells for hair growth.

Cattle skin has leptin which might control skin and hair growth.

A specific gene mutation causes long hair in Angora rabbits.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

Finasteride exposure harms tadpole reproduction and hormone balance.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

Mouse skin can produce and process serotonin, with variations depending on hair cycle, body location, and mouse strain.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

CYP2B12 enzyme in skin cells converts arachidonic acid into specific bioactive lipids.

Rac1 is essential for proper hair structure and color.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.