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Certain defective glucocorticoid receptor mutants move faster inside cell nuclei and work less effectively.

A new mouse model helps study melanocyte cells using GFP expression.

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

Noncoding dsRNA boosts hair growth by activating TLR3 and increasing retinoic acid.

The LEF-1 binding site enhances gene expression in hair follicles, with other proteins aiding specific regulation.

Mutant cells in hair follicles are influenced by their location and interactions with surrounding cells.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

Humans have ancient DNA from Neanderthals and other lineages in their chromosomes, affecting traits and evolution.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Increasing SSAT makes skin more prone to cancer.

Double-stranded RNA helps regenerate hair follicles by increasing retinoic acid production and signaling.

Activating TERT in mice skin boosts hair growth by waking up hair follicle stem cells.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

A specific gene variation in goats is linked to better growth traits.

The polyG fragment in Hoxc13 protein helps evolve mammalian skin and hair by enhancing gene interactions.

RpoS helps Borrelia burgdorferi survive in hosts and adapt to different environments.

Gene therapy in mice increased lifespan and improved health without causing cancer.

Overexpressing Merkel cell virus proteins in human hair follicles can create clusters of cells that resemble Merkel cell cancer.

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

Atoh1 expression can create new Merkel cells in the skin.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

A new gene mutation causes insulin resistance in a girl and her mother.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

The new delivery system improved raloxifene's skin absorption and effectiveness against cancer cells.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

A KRT32 gene variant causes loose anagen hair syndrome.

The scraggly mutation causes hair loss and skin defects in mice.

Injecting recipient splenocytes into donors' thymus can prevent graft-versus-host disease.