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Androgen receptor inactivation delays skin cancer onset and reduces incidence in mice, with gender differences in susceptibility.

A hair cyst can become cancerous, showing specific keratins from the hair sheath.

Changes in keratin affect skin health and can lead to skin disorders like blistering diseases and psoriasis.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

Activated ras can protect kidney cells from a certain substance that causes cell death.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

Anti-Ku-positive patients often have muscle weakness and autophagy plays a key role in their condition.

A mutation in the KRT74 gene causes tightly curled hair.

Mutations in hKAP1 genes may cause hereditary hair disorders.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

SGK3 is essential for proper hair growth and health.

The research created a detailed map of skin cells, showing that certain cells in basal cell carcinoma may come from hair follicles and could help the cancer grow.

Trichilemmal carcinoma shares genetic traits with other skin cancers, suggesting similar treatment options.

BMP signaling helps prevent skin tumors by blocking cancer-promoting pathways.

The Walleye dermal sarcoma virus cyclin causes excessive skin cell growth in mice.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

AP-1 controls tumor cell type by affecting key signaling pathways.

BKN-1 antibody targets specific keratin in basal cell epithelioma and normal skin basal cells.

Mouse models help study genetic skin diseases.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

Overexpressing 14-3-3σ in mice skin reduces cell growth and hair density.

Mouse keratin 6 isoforms have different expression patterns in various tissues.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

Loss of Ten1 in mice causes telomere shortening and symptoms similar to human dyskeratosis congenita.

Melanocyte stem cells can become melanoma, resembling human melanoma.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.