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Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

Nephronectin is linked to worse breast cancer outcomes and helps cancer spread.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

Claudin expression changes help the skin respond to injury.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Genetic testing is crucial for diagnosing and treating acrodermatitis enteropathica effectively.

The Ysc84/SH3yl1 protein family is important for cell movement and the process of taking in materials by interacting with actin and cell membranes.

Fetal environments contain various chemicals that may disrupt hormones.

Intersex frogs have different brain gene activity related to sex and thyroid hormones.

PDRN may reduce inflammation and complications in revision rhinoplasty for patients with high fibrinogen levels.

Pesticides can cause reproductive and adrenal health issues.

Electron Beam Tomography (EBT) is a useful additional test to stress testing for detecting heart disease.

Changing YBX1 protein activity affects skin stem cell function and aging.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

Certain genes in Iranian sheep are linked to wool production and heat adaptation.

CTCF protein is essential for skin and hair follicle development in mice.

A new compound was made that might help treat diseases related to male hormones.

Filaggrin mutations are linked to atopic dermatitis and help explain how genetics and environment affect the disease.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

A new gene mutation linked to a skin condition was found in a Spanish family.

Neprilysin is important for hair growth regulation.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

Enzyme replacement therapy may help alleviate symptoms in complex cases like this.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Hairless protein and putrescine regulate each other, affecting hair growth and skin balance.

Keratins are crucial for cell structure, growth, and disease risk.

Abrocitinib is being evaluated for safety and effectiveness in treating moderate to severe atopic dermatitis.

The study identifies the pheromone gland's location and structure in Endoclita vietnamensis, aiding future pest control methods.

Phospholipids help plant proteins move by regulating receptor interactions.

Erosive pustular dermatosis is a rare skin disease that's hard to treat and affects the scalp or legs.