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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.

DMBT1 and galectin-3 may help suppress epithelial skin cancer.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

Activating Tgr5 may help treat hair loss and bone loss.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

Genetic factors influence growth and brain development in children.

Keratin 16 delays skin maturation and affects skin and hair development in mice.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

A man with itchy skin lesions and weight loss was diagnosed with a rare skin condition linked to a pancreatic tumor.