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Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Shrinking skin cancer increases the chance of cancer in nearby lymph nodes.

Dihydrotestosterone causes p27 protein breakdown in ovarian and breast cancer cells by binding with SKP2.

Miz1 is essential for proper hair structure and growth.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Recognizing minor skin lesions can help identify serious cancer syndromes.

The dog's skin condition improved after removing a tumor that was causing hormone imbalances.

A standardized scoring system is needed to improve model reliability for predicting hair loss in brain tumor patients treated with proton therapy.

Hair repigmentation can indicate malignancy and should be investigated.

A mutation in the human hairless gene causes alopecia universalis.

Trichilemmoma, BCC, and SCC tumors have different stem cell marker expressions.

A rare skin tumor with bone formation was successfully removed without recurrence.

Melanocytic matricoma can look like skin cancer but is usually harmless; surgery and follow-up are advised.

LRIG1 is linked to better survival in Merkel cell carcinoma.

A young woman had a rare scalp tumor usually found in older women.

The research found changes in gene expression related to cell death in mouse skin that help understand hair follicle development and skin health.

A unique gene mutation was found in a family with monilethrix.

Human basal cell carcinomas and squamous cell carcinomas have unique gene expression patterns not fully mirrored in mouse models.

Hair dye ingredient PPD causes cell death and aging in human hair cells by altering microRNA levels.

Keratin 17 is crucial for cell growth in wound healing by aiding protein synthesis.

The Shaven mutation in mice affects hair growth and causes a greasy coat due to abnormal lipid content.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

LDE225 is a promising skin-applied treatment for basal cell carcinoma with good skin penetration and effectiveness.

Basal cell carcinomas in mice can start from hair follicle stem cells and other skin cell types, depending on signaling levels.

Most patients experienced mild to moderate skin problems during a trial for a desmoid tumor treatment.

Cancer risk is linked to the balance of mutations and environmental factors, not just the number of mutations.