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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 mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

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

Lack of KSR1 stops certain skin tumors in mice.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

NKIRAS2 can suppress certain skin tumors but its effect on cancer varies with context and expression level.

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

Kremen is crucial for proper development and preventing tumors by regulating Wnt signaling.

K25, K27, and K28 are found in all inner root sheath layers of hair, while K26 is only in the cuticle.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Collagen XVII is crucial for skin cell growth and nail health.

High levels of human keratin 16 in mice cause skin lesions and abnormal skin development.

The Kras mutation changes normal cell signals, leading to disrupted tissue structure and potential cancer.

Krokot extract hair tonic is safe and effective for hair growth.

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

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

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

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Keratins are crucial for tissue strength, and mutations in keratin genes can lead to various diseases, highlighting the need for targeted therapies.

K14 expression in young rats differs from adults.

A specific mutation in Kras causes abnormal tissue changes by making a cell signal continuously active, which disrupts normal cell coordination.

Two new gene clusters important for hair formation were found on human chromosome 11.

Mouse and human keratin 16 can both form filaments, with differences likely due to the tail domain, not the helical domain.

Two new gene clusters important for hair formation were found on human chromosome 11.

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

A 17-year-old girl with Kartagener's syndrome also has unusual skin, hair, and nail issues.

Keratin 19 forms less stable and shorter filaments than keratin 14, giving unique traits to certain skin cells.

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

K31 can identify clear secretory cells in human sweat glands.