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Certain immune system genes are linked to a higher risk of psoriasis and psoriatic arthritis, while others may offer protection.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

EGF controls hair growth by regulating hair follicles' growth phases.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

The vector successfully directed specific gene expression in hair follicles.

Fibroblasts from healthy donors can prevent changes seen in recessive epidermolysis bullosa simplex.

Hedgehog signaling controls hair follicle development and can affect skin cancer growth.

EGF and EGFR are essential for goat fetal skin development.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

Specific mutations in a receptor cause facial abnormalities and hair loss.

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

EGF–FGF2 helps mouse stem cells grow and become more like nerve cells.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

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

Hirsute women have lower type 2 17β-HSD enzyme levels, which improve with treatment.

EGFR helps control how hair grows and forms without needing p53 protein.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Two new gene clusters important for hair formation were found on human chromosome 11.

Hair root sheaths can be used to accurately analyze genetic markers.

PTEN helps control the number and health of skin stem cells by working with the protein BMAL1.

Mutations in the hairless gene cause a rare form of permanent hair loss.

Two new gene clusters important for hair formation were found on human chromosome 11.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

A boy with severe immune deficiency and Epstein-Barr virus died from high-grade B-cell lymphoma.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

Seven genes are highly expressed in both germ-line and hematopoietic stem cells.