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The cerium-polypeptide hydrogel effectively heals drug-resistant bacterial wounds by fighting bacteria, reducing inflammation, and promoting tissue repair.

Chemokine signaling is important for hair development.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Erythropoietin overexpression disrupts hair growth and fat formation in mice.

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

The new antibody, TYHF-1, specifically targets certain hair-related structures.

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

Human hair keratin might be good for filtering out harmful substances from water.

Ecklonia cava extract can reduce the damage and stress caused by hair dye.

Specific mutations in a receptor cause facial abnormalities and hair loss.

Tofacitinib effectively improved severe skin symptoms in a patient with Hypohidrotic Ectodermal Dysplasia.

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

Longer treatment with vismodegib lowers relapse risk in basal cell carcinoma.

Promising cancer treatments were found, but the manufacturer closed.

The new anti-acne treatment HA-P5 effectively reduces acne by targeting two key receptors and avoids an enzyme that can hinder treatment.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

A protein called IL-36γ causes skin side effects from certain cancer treatments when combined with a common skin bacteria.

Adapalene, Diosmin, and Azelastine could be repurposed to treat onchocerciasis.

The upper hair follicle is stable, while the lower part allows movement during hair growth.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

ZD1839 can cause skin issues like acne and hair changes.

Certain gene changes in osteopontin are linked to higher risk of atopic dermatitis and asthma.

CD98hc's role in skin health decreases with age.

Higher SRD5A2 expression predicts better response to finasteride in treating urinary symptoms.

ACKR2 helps prevent skin scarring and hair loss by controlling inflammation.

Neprilysin is important for hair growth regulation.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

CI-1033 causes skin lesions in rats, similar to humans, due to EGF receptor inhibition.

New LPA receptors (LPA4, LPA5, LPA6) have diverse roles in the body.

Iressa often causes skin issues like acne and dryness in lung cancer patients.