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The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

Blocking certain immune signals can reduce skin damage from radiation therapy.

KGS1 tablets improved skin and hair health.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

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

KRDQN effectively predicts adverse drug reactions with high accuracy and clear explanations.

Long-term data and a team approach are needed to manage chronic side effects from cancer treatments.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

Decreasing MIG6 can increase the movement and invasiveness of MEK-inhibited mutant NRAS melanoma, particularly when stimulated by EGF.

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The Seoul International Dermatology Symposium was a successful event that highlighted new dermatology treatments and fostered international relations.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

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

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A cluster of 21 keratin-associated protein genes important for hair growth was found on human chromosome 21.

The KRTAP22-2 gene in sheep does not significantly affect wool traits.

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

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.