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Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

The naked mutation in mice causes hair loss and helps identify keratin genes.

Mefloquine, an antimalarial drug, is effective in killing melanoma cells resistant to other treatments by causing lethal stress in the cells.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

Melanoma development can be linked to the breakdown of skin's melanin-producing units.

MITF and WNT3A are key in Dun Mongolian horse pigmentation.

We need more research on human hair follicle pigmentation, not just mouse models.

Chemotherapy reduces splenic melanin in mice.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

A human serum-enriched medium effectively supports melanocyte growth and activity without using animal-derived supplements.

An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

Melanocyte stem cells in hair follicles are key for hair color and could help treat greying and pigment disorders.

Activating β-catenin increases melanocytes and decreases Schwann cells.

Wnt10b helps hair follicle cells mature and produce pigment.

Mutations in the Whn gene affect hair keratin gene expression differently.

The N gene affects the protein makeup of mouse hair.

CD34+ and CD34- melanocyte stem cells have different regenerative abilities.

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

Melanocyte precursors in human fetal skin follow a specific migration pattern and some remain in the skin's deeper layers.

Researchers identified potential markers for human hair color stem cells.

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

Increased methylation of the Filip1l gene may contribute to aggressive skin cancer.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Melatonin may help whisker growth in mice.

Cyclophosphamide likely causes skin darkening by affecting hair follicles.

Agouti and AGRP affect pigmentation and obesity, with implications for metabolic disorders.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.