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Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.

Higher expression of the keratin-associated protein 8.1 gene in Liaoning cashmere goats is linked to finer cashmere fibers.

The ABI1 gene contributes to prostate cancer progression and treatment resistance.

Gene therapy with a vitamin D receptor gene improved hair growth in rats with a type of rickets-related baldness.

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

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

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

Dickkopf-related Protein 2 can help hair grow by activating a specific cell pathway.

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

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

A stable, active version of a growth factor was made in bacteria, showing promise for medical use.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Too much AKR1C3 enzyme causes resistance to finasteride by increasing testosterone.

Certain KIR genes in Indian SLE patients are linked to disease severity and could be biomarkers.

Brg1 is crucial for keeping hair follicle stem cells and repairing skin, working with the Sonic Hedgehog pathway to promote hair growth.

HPV8 causes hair follicle stem cells to grow, leading to skin lesions.

FGF13 gene changes cause excessive hair growth in a rare condition.

Silencing SFRP1 alone promotes hair growth, but adding DKK1 does not help.

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

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

AKR1C3 could be a treatment target for metabolic issues in PCOS.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

Different body areas have unique skin cell communication patterns, explaining why certain skin diseases occur in specific regions.

Removing both Atr and Trp53 genes in adult mice causes severe tissue damage and death due to DNA damage.

The hHa7 gene is regulated by androgens in certain body hair, not scalp hair.