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

A KRT32 gene variant causes loose anagen hair syndrome.

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

A new gene variant causes curly coats in some dog breeds.

The STRIPAK complex is crucial for skin cell organization and creating a functional skin barrier.

The dog's health improved after treatment with antibiotics and other medications.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

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

The P133R mutation in AKR1D1 enzyme causes harmful bile acid buildup, explaining related health issues.

ADAM 10 and ADAM 12 proteins are involved in different stages of hair growth and could be targets for treating hair disorders.

AKR1B10 enzyme may cause keloid scars and could be a treatment target.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

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

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

Blocking mTORC1 reduces skin tumor growth in mice.

Different androgen concentrations affect wool-related gene expression differently in Hetian and Karakul sheep breeds.

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

Hoxc13 and hair keratin are needed for forming rough skin on frog mating pads.

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

Keratin-associated proteins may have roles in various mouse tissues, not just hair.

Rapamycin reduces skin cell growth and tumor development by affecting cell signaling in mice.

Kerion is a severe scalp infection that needs quick treatment to avoid permanent hair loss in children.

Different keratins have unique expression patterns in mouse skin cells.

Lack of KSR1 stops certain skin tumors in mice.

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

Kaposi's sarcoma lesions might originate from benign tissue changes.

The KDM1 gene helps Venus flytraps close by managing potassium ions.