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Mice with too much sPLA₂-IIA have hair loss and poor wound healing due to abnormal hair growth and stem cell depletion.

S100a4 is key for hair growth in cashmere goats.

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

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

Overexpressing SSAT enzyme reduces prostate tumor growth in mice.

A genetic variant linked to hair thinning in Japanese women was found.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Overexpression of sPLA2-IIA in mouse skin reduces hair stem cells and increases cell differentiation through JNK/c-Jun pathway activation.

A specific gene mutation causes woolly hair and hair loss.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Mutations in the Sgk3 gene cause fuzzy hair in mice.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Woodhouse-Sakati syndrome shows varied symptoms and genetic differences within families.

The 14-3-3σ gene is essential for preventing hair loss.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

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

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

A specific gene mutation causes varying hair loss severity in a Pakistani family.

A new mutation in the HR gene causes hair loss in a specific family.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.