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A gene variant increases the risk of a type of hair loss by affecting hair protein production.

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

The condition is linked to chromosome 12, but no mutations were found in the known genes.

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

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

A gene called HDAC9 might be a new factor in male-pattern baldness.

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

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

A specific gene mutation causes congenital hair loss.

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

Researchers found a gene mutation responsible for a rare hair loss condition.

Type I and Type II keratin chains can form heterodimers despite sequence differences.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

Skin cells and certain hair follicle areas produce hemoglobin, which may help protect against oxidative stress like UV damage.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21.

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

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Hair differentiation starts earlier than thought, involving multiple type-II keratins.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

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

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.