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

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

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

The protein CTCF is essential for skin development, maintaining hair follicles, and preventing inflammation.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

Mouse skin cancer progression involves a unique group of cells marked by ABCG2 and MTS24.

Identical p53 gene mutations in different cancers suggest the need for careful treatment.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

Some leukemia treatments can cause skin reactions similar to keratosis pilaris.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

K6hf is found in specific parts of hair follicles, nails, and tongue, and is linked to hair growth and structure.

Blocking YAP/TAZ could be a new way to treat skin cancer.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

ETC-159 was safe up to 30 mg, but no tumor shrinkage was seen.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Melanocyte-associated antigens may play a key role in alopecia areata and could be targets for new treatments.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

Sfrp2 increases during hair follicle catagen phase and slows keratinocyte growth.

KIT's role in skin cells is not entirely independent, as other cells can influence its function.

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

TYK2 inhibitors show promise for treating cancer and autoimmune disorders.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

HPV8 causes hair follicle stem cells to grow, leading to skin lesions.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Krt15+ cells in the mouse intestine resist radiation and can start tumors.