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Removing UBE2N from skin cells causes inflammation and immune response, which can be lessened with specific inhibitors.

MPA increases cancer spread by boosting Eph A2 activity.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

New treatments for a type of skin cancer show promise but have side effects and may work better with other therapies.

Tebentafusp-tebn improves survival rates in uveal melanoma patients but has common side effects like rash and fatigue.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

EGFR helps hair follicles transition properly by controlling Stathmin levels.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Overexpression of PKCepsilon leads to increased TNFalpha, promoting metastatic squamous cell carcinoma in mice.

Androgen receptor overexpression can increase prostate cancer cell growth even without hormones.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

The PP2A-B55α protein is essential for brain and skin development in embryos.

A 12-year-old girl was misdiagnosed with alopecia areata but actually had a nevus sebaceus with a genetic mutation.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Loss of Pten in certain hair follicle stem cells increases skin cancer risk.

Removing integrin α3β1 from hair stem cells lowers skin tumor growth by affecting CCN2 protein levels.

Hair follicle regeneration may slow tumor growth.

EGFR deficiency in skin causes hair follicle issues and inflammation.

Retinoic acid-binding proteins in skin are regulated by β-catenin and Notch signalling.

A pathway helps maintain long telomeres in both stem and cancer cells.

Overexpression of ALK2 in hair follicles disrupts skin development and slows wound healing.

A rare gene variant causes hair and nail issues in a family.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Genetic testing for EGFR mutations is crucial in similar cases.

Human dermal fibroblasts are the main cells targeted by a virus that can cause a deadly skin cancer, and a certain inhibitor can effectively block this infection.

BSSP may help skin tumors grow and could be a marker or target for skin cancer treatment.

KRT72 gene helps form hair.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Axitinib treatment turned a man's grey hair back to black.