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

Certain genetic variations can make people more likely to experience hair loss and low white blood cell count from azathioprine.

Alopecia areata is influenced by genetics and immune system factors, and better understanding could improve treatments.

Mutant cells in hair follicles are influenced by their location and interactions with surrounding cells.

CTLA4 gene variants are not linked to alopecia areata in Monterrey's Mexican population.

Certain genetic markers on the Y-chromosome may influence prostate cancer risk in Iraqi males.

The Agouti gene influences pigmentation and may have a developmental role in deer mice.

Certain gene variations increase the risk of alopecia areata in Koreans.

A mouse gene mutation increases the risk of skin cancer.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

MOF controls skin development by regulating genes for mitochondria and cilia.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

Introducing the OTC gene improved symptoms in mice with OTC deficiency.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

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

Arg1+ macrophages may play a role in causing alopecia areata.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

Certain genetic variations in IL-16 may increase the risk of alopecia areata.

Mutations in certain skin proteins cause severe skin issues, while others have limited effects, highlighting the need to understand these proteins for better treatments.

Alopecia areata may be linked to atopic diseases like eczema, asthma, and allergies.

A specific gene mutation causes woolly hair and hair loss.

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

Certain gene variations may increase the risk and severity of alopecia areata.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.