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The research cloned keratin 7 genes from humans, mice, and marsupials, found similarities between human and mouse genes, and discovered new areas of K7 expression in mice.

A gene mutation causes curly hair and hair loss in rats.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

Krt15+ cells in the mouse intestine resist radiation and can start tumors.

KRTAP2-3 could help predict cancer recurrence by identifying specific cancer cells.

Krt15+ cells in mice can resist radiation, regenerate tissue, and start tumors, suggesting new cancer treatment targets.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

TRIV-509 quickly improves skin barrier and cell health in atopic dermatitis.

KRT17 may be a new target for endometrial cancer treatment because it helps cancer cells move and form new blood vessels.

KRTAP2 genes are crucial for hair structure and may impact hair disorders and treatments.

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

HPV8 E6 gene causes growth of certain skin stem cells.

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

Krtap11-1 is important for hair strength and structure.

Keratin K6irs is a marker for the inner root sheath of hair follicles in mice and humans.

The study created a mouse model to better understand hair follicle stem cells' role in hair growth and repair.

Keratins K6 and K16 are expressed more freely in regenerating mouse skin than K1 and K10.

Keratins 8 and 14 can help identify and diagnose benign skin tumors.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

K31 can identify clear secretory cells in human sweat glands.

KRTAP10 proteins help form the hair shaft's tough outer layer by interacting with specific hair keratins.

Lack of KSR1 stops certain skin tumors in mice.