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A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Patched1 helps prevent tumors by controlling cell growth.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

Monilethrix causes fragile, patchy hair loss.

Ossification in trichilemmal cysts is more common than previously believed.

Msx-2 gene removal speeds up skin wound healing in mice.

Cysteines in wool fibers are accessible and form important disulfide bonds.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Neutrophils quickly respond to skin injury.

Loose anagen hair syndrome is caused by structural abnormalities in the hair follicle's inner root sheath.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

Laser treatment can fix skin color issues after syndactyly surgery.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Proper niche formation in Drosophila requires Slit-Robo signaling for cell migration.

Nail issues are common in alopecia areata patients.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

The naked mutation in mice causes hair loss and helps identify keratin genes.

Ablative fractional laser treatment nearly matches the gene reduction effects of topical vismodegib in skin cancer.

Using titanium mesh and thigh tissue is effective for complex scalp reconstruction.

Using a special knife helps improve hairline scars from surgery.

Disrupting β-catenin signaling in certain cells causes anorectal malformations.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

Specific keratin gene mutations can cause monilethrix.

Li2CO3 improved skin disease in a mouse model of Focal Dermal Hypoplasia without toxicity.