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

A rare skin condition causes red, dark, bumpy facial lesions.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

TACE/ADAM17 is essential for maintaining healthy hair and hair follicle stem cells.

Epidermal growth factor helps hair recover after chemotherapy.

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

Mutations in the p63 gene affect skin adhesion, barrier integrity, and hair growth.

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

Keratins are crucial for cell structure, growth, and disease risk.

PRSS35 enzyme may help start skin tumors and could be a target for cancer treatment.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

Activated erbB-2 in mice skin causes severe skin and hair abnormalities.

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Trichohyalin helps in hair and skin cell structure and function by binding calcium and linking proteins.

Foxp1 helps control hair stem cell growth and response to stress during hair growth cycles.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

HIF-1α in fibroblasts boosts hair growth and health.

FOXN1 gene variants cause low T cells and immune issues from birth.

Sheep cells were successfully modified to include a spider silk protein gene.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

Most genetic mutations causing hypohidrotic ectodermal dysplasia in Russian patients are found in the EDA gene.

Inactivating β-catenin is essential for chick retina regeneration.