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A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

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

CARASIL can cause different symptoms even with the same genetic mutation.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

Mitochondrial features can predict colorectal cancer outcomes and improve immunotherapy.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

Increasing SSAT makes skin more prone to cancer.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Certain gene combinations may affect prostate cancer risk, and GSTP1 methylation is linked to tumor aggressiveness.

Defective mitochondrial DNA replication causes aging symptoms and increased oxidative damage in mice.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

A gene mutation in mice causes permanent hair loss and skin issues.

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

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

Certain genetic markers may increase or decrease prostate cancer risk.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

Loss of Dnmt3a and Dnmt3b leads to more aggressive skin tumors, but blocking PPAR-γ can reduce this effect.

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

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.