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Small molecules KY19382 and KY19334 may help treat skin cancer by reducing CDK1 levels and blocking harmful cell signals.

Natural gene therapy shows promise for treating skin disorders like epidermolysis bullosa.

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

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

Rat dermal papilla cells have unique genes crucial for hair growth.

Eupafolin nanoparticles help protect skin cells from damage caused by air pollution.

Exosomes from stem cells help improve nerve repair in rats.

EGFR is essential for organized skin nerve growth and branching.

RXRa is crucial for Th2 immune cell development and may link nutrition to immune health.

The gene Endothelin 3 makes mice's fur darker by increasing pigment cells and pigment levels.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

NIR-II imaging effectively tracked stem cells that helped repair facial nerve defects in rats.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

TNFα and interleukin-1 blockers reduce skin inflammation from EGFR antibody therapy.

TNFα and interleukin-1 blockers reduce skin inflammation from EGFR antibody therapy.

Trichotillomania, a disorder where people compulsively pull out their own hair, often starts around age 12, is more common in adult females, and can be treated with behavior therapy and medication.

Sweat gland development involves two unique skin cell programs and a temporary skin environment.

Local injections of nanosized rhEPO can speed up skin healing and improve quality after deep second-degree burns.

Umbilical cord blood transplantation improved the boy's symptoms despite complications.

17β-estradiol boosts APE1/Ref-1 secretion in cells and mice via a calcium-dependent pathway.

Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

Finasteride helps female-pattern hair loss.

ANXA1 influences hair growth in mice through the EGF signaling pathway.

A new rat strain with a specific gene mutation causes hair loss and kidney issues.

A man with Acrodermatitis continua did not get better with etanercept treatment, and his condition worsened, suggesting treatment effectiveness may vary by genetics and race.

MITF and WNT3A are key in Dun Mongolian horse pigmentation.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.