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Overexpressing Merkel cell virus proteins in human hair follicles can create clusters of cells that resemble Merkel cell cancer.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

Patched1 helps prevent tumors by controlling cell growth.

The transgene likely activated an oncogene or interrupted a tumor suppressor gene, causing melanoma in mice.

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

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

EGFR helps control how hair grows and forms without needing p53 protein.

Hair shaft changes may be linked to CCCA, but their role is unclear.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

Matriptase is crucial for skin barrier, hair growth, and may contribute to skin cancer.

The p53 protein has complex, sometimes contradictory functions, including tumor suppression and promoting cell survival.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

Trypsin slows hair growth and affects color by causing cell death in hair follicles.

T cell subsets are crucial in kidney cancer, and a new model predicts patient outcomes using key genes.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

Increasing PDCD4 protein may help prevent or treat some skin cancers.

SOX4 is crucial for the development of melanoma.

Blood tests for tumor cells could improve prostate cancer diagnosis and treatment; hair loss severity linked to a gene affecting prostate conditions.

GLI1 might protect against the start of skin cancer and is not linked to cancer severity.

PINK1 is important for controlling gut immune responses linked to early Parkinson's disease.

ETS2 is crucial in squamous cell carcinoma development and could be a therapeutic target.

BST2 protein and certain T cells increase in early alopecia areata.

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

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Some people with chronic hair loss may have thyroid autoimmunity.

A new genetic mutation was found causing hair and eye issues in a boy.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.