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

The new AI software predicts melanoma outcomes more accurately than traditional methods.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

MITF+ melanoma patients are more likely to have multiple melanomas and unique skin patterns.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

IL-15 helps maintain hair growth and protects the immune status of hair follicles.

B6.Cg-Tyr c−2J Hr hr /J mice have a stronger delayed sunburn reaction and are good for UV research.

MG53 helps reduce skin damage caused by nitrogen mustard.

ILC1-like cells may contribute to hair loss in alopecia areata.

Different keratins have unique expression patterns in mouse skin cells.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Hair repigmentation can indicate malignancy and should be investigated.

Malt1 protease is essential for regulatory T cell function and could be targeted to boost antitumor immunity.

CCCA may be caused by both hair traction and an immune response.

Human dental pulp stem cell-conditioned medium, especially from hypoxic conditions, may help treat chemotherapy-induced hair loss and does not increase cancer risk.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Hair cortisol measurement can help diagnose and monitor Cushing’s disease.

Hedgehog pathway inhibitors could be effective in treating melanoma.

The study developed a mouse model for Alopecia Areata that responds to treatment, useful for future research.

Higher levels of MIG and IP-10 may help diagnose and monitor Alopecia Areata.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

The mtDNA N haplogroup is linked to a higher risk of late-onset lupus and specific symptoms in Han Chinese women.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Human hair follicles have their own thyroid hormone system.

Mitf plays a key role in melanoma progression and is linked to disease stage.