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

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

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

Normal cells outcompete and remove mutant cells in the pancreas with the help of the EphA2 receptor.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

Activating Kras in mouse skin causes excess skin and hair loss.

Mutations in the KRT85 gene cause hair and nail problems.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.

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

A KRT32 gene variant causes loose anagen hair syndrome.

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.

Hair loss in certain mice is linked to changes in keratin-related genes.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

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

Krtap11-1 is important for hair strength and structure.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

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

A genetic variant in the KRT25 gene causes tightly curled hair.

Mutations in keratin genes can cause skin and mucosa disorders.

A mutation in the KRT25 gene causes woolly hair and hair loss.

A mutation in the KRT82 gene is significantly associated with Alopecia Areata.

Melanocyte pathology requires keratinocyte hyperplasia and regulation dysfunction.

The KRTAP gene family helps understand hair evolution and hair disorders.

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

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

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

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.