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Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Protein kinase C epsilon may increase skin cancer risk by affecting nearby cells.

A 68-year-old woman with benign mucous membrane pemphigoid has eye, mouth, and skin issues, including thick plaques and nail changes.

Lichen planopilaris can be triggered by prolonged scalp traction and can be treated with corticosteroids.

Sporadic trichoblastic neoplasms generally don't recur or spread, with one case showing a specific genetic fusion.

Kerion in Fars Province mainly affects boys under 11 linked to animal contact, with varied treatment outcomes.

Artificial dermis used for hair transplantation can reconstruct scalp defects effectively without the need for tissue expansion.

Seborrheic keratosis likely originates from the upper regions of hair follicles.

Skin RAGE levels are linked to inflammation and cell death.

Trichilemmal carcinoma is rare, usually benign after removal, but needs close follow-up due to recurrence risks.

Cells from concentrated growth factor can become different cell types.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

The human K5 promoter controls specific gene expression in skin cells, with key regulatory elements near the TATA box.

ErbB2 signaling is crucial for skin cell growth and cancer development in mice.

New treatments using stem cells and special materials show promise for severe eye surface disease.

Scalp hair follicle cells help protect and heal skin in certain skin conditions.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Mast cells may significantly contribute to central centrifugal cicatricial alopecia.

Spontaneous keloids may be linked to nephrogenic systemic fibrosis in dialysis patients.

EGFR signaling is crucial for skin and hair health, and targeting it could help treat skin diseases and cancer.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

Overexpression of LRIG3 in skin causes hair loss.

PmtHEE is a better model for studying pigmented skin because it includes melanocytes and shows improved cell differentiation.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

Vogt-Koyanagi-Harada disease affects vision and skin, mainly in people with darker skin, and is treated with steroids and immunosuppressants.

Targeting specific T cells may help treat alopecia areata.

Activating certain hair follicle cells could prevent hair loss from cancer treatments.