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The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

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

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

Lack of KSR1 stops certain skin tumors in mice.

WWOX deficiency in mice causes skin and fat tissue problems due to disrupted cell survival signals.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

ETC-159 was safe up to 30 mg, but no tumor shrinkage was seen.

Targeting the TNFRSF1B gene may help treat hair loss.

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

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

The lanceolate hair-J mutation in mice helps understand human hair disorders like Netherton's syndrome.

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

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

The FOS gene helps hair growth in Tan sheep.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive forestomach cancer.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

ErbB2 signaling is crucial for skin cell growth and cancer development in mice.

Keratinocytes can reverse the effects of the GNAQ oncogene, inhibiting melanoma cell growth.

PBX1 helps hair stem cells grow and change by turning on certain cell signals and preventing cell death, which may be useful for hair regrowth treatments.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

New mutations in the hairless gene may cause hair loss and affect bone development.

Lhx2 helps retinal cells respond to signals for eye development.

Removing Sprouty genes in mice causes various hormone-related issues but does not increase cancer risk by one year of age.

Mutations in the SNRPE gene cause hereditary hair loss.