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Urotensin II increases growth and VEGF production in rat skin cells by turning on the Wnt-β-catenin pathway.

The new aptamer TAGX-0003 shows promise as an effective treatment for hair loss disorder alopecia areata.

A new DSG4 gene mutation causes hair defects in a young girl.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

The enzyme from human skin can cross-link proteins and needs calcium to work.

Immune activities and specific genes are important in male pattern baldness.

Gut bacteria can lower androgen levels in male mice.

Two gene areas linked to male pattern baldness found, more research needed.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

Overexpressing AVP1 and AtNHX1 in plants improves salt tolerance and root hair development.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

The enzyme PA-PLA1α is important for proper hair follicle development.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

A gene mutation causes curly hair and hair loss in rats.

Proteins from Tianshan red deer abomasum have strong anti-inflammatory, anti-tumor, and antioxidant effects.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

AIMP1 can boost hair growth by increasing stem cell activity.

Gap junctions help control feather pattern formation by enabling cell communication.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Two specific genetic markers increase the risk of hair loss in Asian populations.

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

Researchers found two new genetic variants linked to Alzheimer's disease.

Blocking CYP17A1 enzyme may help improve certain brain function issues related to dopamine.