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Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

LHX2, with other markers, can identify hair placodes in rats.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

A new gene mutation is linked to monilethrix in the studied family.

HDAC6 helps keep ovarian follicles dormant, extending female fertility.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

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

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

CK 19 expression is higher in more severe skin cancers.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

hHb1, hHb3, and hHb6 mRNAs start expressing at the same time in hair follicles.

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

hHbl gene is active in hair shaft cells and some pilomatricomas.

A mutation in the human hairless gene causes alopecia universalis.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.