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Protein kinase C epsilon may promote skin cancer development after UV exposure by affecting nearby cells.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

BBS7 is essential for healthy gums by supporting cell function and blood flow.

A new pair of mouse keratins, 65 kD and 48 kD, are found in specific skin areas and are linked to a unique skin differentiation type.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

A specific DNA region controls skin cell gene expression by working with certain proteins.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

A chimeric keratin partially improved skin structure in mice lacking keratin 5, but didn't fully restore normal skin.

A rabbit gene important for hair development was identified and detailed.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

Removing both KLK5 and KLK7 proteins can prevent death and skin issues in Netherton syndrome.

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

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

Wnt7a helps corneal cells grow and stick together, aiding in repair.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

Keratin 6A increases skin inflammation, suggesting it could be a target for treating certain skin diseases.

Acidic keratin genes are on CFA9 and basic keratin genes are on CFA27 in dogs.

Mutations in hKAP1 genes may cause hereditary hair disorders.

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

Too much keratin 16 in mice skin causes abnormal skin thickening and structure.

The human K5 promoter controls specific gene expression in skin cells, with key regulatory elements near the TATA box.

Mice with human skin protein K8 had more skin problems and cancer.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

T cell subsets are crucial in kidney cancer, and a new model predicts patient outcomes using key genes.

Eating a lot of fat increases PKCβ and inflammation in skin fat cells, which affects skin and hair health.

Only one K16 gene on chromosome 17 makes a functional keratin protein.

The Bsk mutation doesn't involve keratin gene recombination and its cause is unknown.