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Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Specific keratin gene mutations can cause monilethrix.

SV40 T antigen in hair follicles causes abnormal hair and health issues in mice.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

A mutation in the human hairless gene causes alopecia universalis.

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

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

A specific gene mutation causes complete hair loss in an Irish Traveller family.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

The naked mutation in mice causes hair loss and helps identify keratin genes.

S100A4 promotes aggressive ovarian cancer and is a potential treatment target.

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

A specific gene mutation causes severe skin and nail issues and hair loss.

A gene mutation in mice causes skin defects and early death.

A new mouse mutation causes skin and hair defects due to a gene change.

Early and accurate diagnosis of congenital smooth muscle hamartomas is crucial to distinguish them from other conditions.

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

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

The cancer gene c-Myc increases harmful chemicals that damage DNA and can lead to cancer, but antioxidants can reduce this damage.

BSSP may help skin tumors grow and could be a marker or target for skin cancer treatment.

DNA virus-induced tumors have consistent isozyme profiles, unlike other tumor types.

Polyamines are crucial for skin tumor development, and inhibiting them can prevent tumors.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

Keratin 10 end domains may increase skin cancer risk by reducing cell death.

The scraggly mutation causes hair loss and skin defects in mice.