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CuATSM speeds up wound healing and reduces scarring.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

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

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

The scraggly mutation causes hair loss and skin defects in mice.

New mutations in the DSG4 gene cause a rare hair condition.

Mutations in specific llama genes may affect fiber quality for textiles.

Researchers converted human embryonic stem cells into trophoblast stem cells using specific transcription factors.

Overexpressing NSD3 in mice causes breast cancer-like tumors and gland abnormalities.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

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

Steroid sulfatase in hair follicles may be a target for treating hair loss.

The KRTAP36-1 gene affects wool quality in Chinese Tan lambs.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

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

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Aging in one type of stem cell can cause aging-like changes in various organs.

Genetic factors influence growth and brain development in children.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

TSC2-/meth cells can cause skin lesions, hair growth, and lung issues, and may be treated with chromatin remodeling agents.

S100A4 promotes aggressive ovarian cancer and is a potential treatment target.

A protein called lfTSLP is important in causing allergic and other skin diseases and could be a target for treatment.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Mutations in the SNRPE gene cause hereditary hair loss.

Two genetic variations in Moa buffalo help them adapt to heat.

Enzyme purified and characterized for minoxidil sulphation in rat liver.