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A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

Grasp protein helps maintain skin health after UVB exposure.

Artemis phosphorylation at Ser516 may help regulate skin and hair structures.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

A rare genetic disease caused severe, worsening hair loss from early childhood with poor treatment results.

Certain proteins, caspases-1 and -11, are important in the early development of skin inflammation in mice.

SNP rs2479106 in the DENND1A gene may increase PCOS risk in Saudi Arabian females.

Escin may help treat hair loss by boosting a specific cell growth pathway.

DNMT1 may help treat hypospadias by improving cell function and preventing unwanted cell changes.

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

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

Zfp157 is active in many mouse tissues during development and in specific adult cells.

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

Deleting the Sox21 gene changes hair lipid composition and increases cholesterol sulfate levels.

CRABP1 boosts hair cell growth in Hu sheep by affecting key genes.

The most common sign of aging at the gene level is more Ectodysplasin A2 Receptor (EDA2R) being made.

The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

A protein called sFRP4 from skin cells stops the development of pigment-producing cells in hair.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

Neuropilin 2 may be a biomarker for melanoma and affects melanocyte behavior.

LSD1 is essential for healthy skin development and creating the skin's protective barrier.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.

A mutation in the Sgkl gene causes defective hair growth in mice.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

SQSTM1 is linked to increased risk of alopecia areata.

The visfatin GT genotype may increase the risk of Alopecia Areata.

The HCR gene contributes to psoriasis risk.

A specific gene mutation causes a severe skin disorder in a family.

Ptprq has multiple forms that change during inner ear development.